Wikipedia:WikiProject Short descriptions/wd/diseases
Explanation
[edit]A list of the different distinct text descriptions currently provided on Wikidata for items in the subtree of disease (Q12136).
Use the 'list' link to get the full list of individual items with a particular description. This can be used to verify what sorts of items have been given the description; to go to their article pages if one wants to add a {{short description}} to override it; or to go to their Wikidata item if one wants to edit it there.
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List
[edit]This list is automatically generated from data in Wikidata and is periodically updated by Listeriabot.
Edits made within the list area will be removed on the next update!
Count | list | Sample_article | Description |
---|---|---|---|
1046 | list | 17q21.31 microdeletion syndrome | Human disease |
446 | list | 17β-Hydroxysteroid dehydrogenase III deficiency | human disease |
58 | list | Abasia | disease |
34 | list | Accessory pancreas | congenital disorder of digestive system |
34 | list | Acneiform eruption | medical condition |
34 | list | Anti-NMDA receptor encephalitis | rare disease |
17 | list | Bladder exstrophy | congenital disorder of urinary system |
17 | list | Asperger syndrome | neurodevelopmental condition |
16 | list | Adrenal gland disorder | endocrine disease |
14 | list | Alexander disease | congenital disorder of nervous system |
13 | list | Arrhinia | congenital disorder of respiratory system |
10 | list | Blanch (medical) | symptom |
9 | list | Blain (animal disease) | animal disease |
9 | list | Attention deficit hyperactivity disorder | range of neurodevelopmental conditions |
9 | list | Acne conglobata | skin condition |
8 | list | Borna disease | horse disease |
7 | list | Cysticercosis | Human helminthiasis |
7 | list | Dhat syndrome | culture-bound syndrome |
7 | list | Aphakia | disorder of lens |
7 | list | Cryopyrin-associated periodic syndrome | syndrome |
6 | list | GM1 gangliosidoses | Lysosomal storage disease |
6 | list | Bovine malignant catarrhal fever | cattle disease |
6 | list | Congenital disorder of glycosylation type IIc | genetic disease |
6 | list | Clinical lycanthropy | mental disorder |
6 | list | Arachnophobia | phobia |
6 | list | Dermatitis | skin disease |
5 | list | Black band disease | coral disease |
5 | list | Canine distemper | dog disease |
5 | list | Amoebic liver abscess | infectious disease |
5 | list | Blight | plant disease |
5 | list | Crimean–Congo hemorrhagic fever | viral disease |
4 | list | Body dysmorphic disorder | Mental disorder |
4 | list | Condyloma | Wikimedia disambiguation page |
4 | list | Cyclopia | congenital disorder |
4 | list | Acrocephalosyndactylia | group of diseases |
4 | list | Cystic fibrosis transmembrane conductance regulator | protein-coding gene in the species Homo sapiens |
4 | list | Amnesic shellfish poisoning | syndrome of shellfish poisoning |
3 | list | Carl and Clarence Aguirre | Conjoined twins |
3 | list | Large-cell lung carcinoma | Disease |
3 | list | Hypergonadism | Medical condition |
3 | list | Coprolalia | Neurological disorder |
3 | list | Blister beetle dermatitis | cutaneous condition |
3 | list | Fungal folliculitis | fungal infection |
3 | list | Fechtner syndrome | genetic disorder |
3 | list | Dysgraphia | neurological condition, developmental or acquired |
3 | list | Cluster headache | neurological disorder |
3 | list | Hyperthyroxinemia | thyroid disease |
2 | list | Abby and Brittany Hensel | American conjoined twins |
2 | list | Coenurosis | Helminthiasis |
2 | list | Infantile neuronal ceroid lipofuscinosis | Neuronal ceroid lipofuscinosis |
2 | list | List of adverse effects of aripiprazole | Wikimedia list article |
2 | list | Angel wing | bird disease |
2 | list | Neglected tropical diseases | class of diseases |
2 | list | Biddenden Maids | conjoined twins |
2 | list | Corn (medicine) | cutaneous disease |
2 | list | Limbic-predominant age-related TDP-43 encephalopathy | form of dementia |
2 | list | Acyanotic heart defect | group-type of congenital heart defects |
2 | list | Diphyllobothriasis | helminthiasis |
2 | list | Achromatopsia | human illness, a type of color blindness |
2 | list | Hepatitis B | human viral infection |
2 | list | Cyanosis | medical sign |
2 | list | Cotard delusion | mental disease |
2 | list | Blue nails | nail disease |
2 | list | African trypanosomiasis | parasitic disease |
2 | list | Haltlose personality disorder | proposed personality disorder |
2 | list | Factitious disorder imposed on self | psychiatric factitious disorder |
2 | list | Jumping to conclusions | psychological term |
2 | list | Catalepsy | psychomotor symptom of catatonia, abnormal maintenance of postures |
2 | list | Delusional misidentification syndrome | psychopathological syndrome |
2 | list | Osteopathia striata | radiologic sign |
2 | list | Disorder of written expression | range of neurological conditions, developmental or acquired |
2 | list | Extrapulmonary tuberculosis | respiratory disease |
2 | list | Gonorrhea | sexually transmitted infection |
2 | list | Periapical granuloma | tooth disease |
2 | list | Acute severe asthma | type of asthma |
2 | list | Spiral fracture | type of bone fracture |
2 | list | Neurofibromatosis type II | type of neurofibromatosis disease |
2 | list | Chylothorax | type of pleural effusion |
2 | list | Closed-head injury | type of traumatic brain injury |
2 | list | Adenomatoid tumor | type of tumor |
2 | list | Arteriovenous malformation | vascular anomaly |
1 | list | Makyo | "Ghost cave": Zen Buddhist concept |
1 | list | Haemodialysis-associated amyloidosis | #946;2M) deposits in the musculoskeletal system leading to carpal tunnel syndrome (CTS), chronic arthropathy, cystic bone lesions, destructive osteoarthropathy, and pathologic fractures |
1 | list | Meth mouth | 'The Shan smile' |
1 | list | Sitosterolemia | (2p21) genes |
1 | list | Mood disorder | (psychology) Any of various disorders characterised by disturbance in an individual's mood |
1 | list | Kaufman oculocerebrofacial syndrome | . An autosomal recessive mode of inheritance seems most likely. |
1 | list | Chronic actinic dermatitis | . Resolution of photosensitivity is reported in up to 50% of individuals after 15 years or more, with contact allergies persisting. |
1 | list | Nutcracker syndrome | 1 mmHg). The thin septae between the veins and the collecting system in the renal fornices rupture, with resultant left sided haematuria. |
1 | list | Dancing plague of 1518 | 16th century mass dancing mania in Strasbourg |
1 | list | Zymotic disease | 19th-century medical term for acute infectious diseases |
1 | list | Microcoria | 2 mm in diameter) from birth, peripheral iris hypopigmentation and transillumination defects leading to errors of refraction (myopia, astigmatism) and sometimes juvenile open angle glaucoma |
1 | list | Piedra | 2 types of piedra white and black |
1 | list | Costeff syndrome | 3-methylglutaconic aciduria that has material basis in mutation in the OPA3 gene |
1 | list | Malpuech facial clefting syndrome | 3MC congenital syndrome associated with the COLEC10 gene on chromosome 8q24 |
1 | list | Michels syndrome | 3MC syndrome associated with the MASP1 gene on chromosome 3q27 |
1 | list | Erosive pustular dermatitis of the scalp | 70 years old) and characterized by the development of painful pustules, shallow erosions, and crusting on atrophic skin that eventually result in cicatricial alopecia |
1 | list | Griscelli syndrome type 2 | A Griscelli syndrome characterized by silvery gray sheen of the hair, hypopigmentation of the skin and immunodeficiency with or without neurologic impairment that has material basis in mutation in the RAB27A gene on chromosome 15q21.3. |
1 | list | Elejalde syndrome | A Griscelli syndrome characterized by silvery gray sheen of the hair, hypopigmentation of the skin and neurological impairment without immunodeficiency that has material basis in mutations in the MYO5A gene on chromosome 15q21.2. |
1 | list | Typhoid fever | A bacterial infectious disorder contracted by consumption of food or drink contaminated with Salmonella typhi. This disorder is common in developing countries and can be treated with antibiotics. |
1 | list | Neurothekeoma | A benign neoplasm arising from nerve sheaths. It is characterized by the presence of a myxoid stroma. |
1 | list | Ovarian fibroma | A benign neoplasm arising from soft tissue of the ovary. It is characterized by the presence of spindle-shaped fibroblasts. |
1 | list | Endocrine gland neoplasm | A benign or malignant neoplasm arising from the epithelial cells of an endocrine organ. Representative examples include pituitary gland adenoma, pituitary gland carcinoma, thyroid gland carcinoma, carcinoid tumor, and neuroendocrine carcinoma. |
1 | list | Thrombocytopenia | A blood platelet disease characterized by a low platelet count in the blood. |
1 | list | Infantile cortical hyperostosis | A bone inflammation disease that causes bone changes, soft tissue swelling and irritability in infants. The disease has been associated with COL1A1 gene. It has symptom soft-tissue swelling, has symptom bone lesions, and has symptom irritability. |
1 | list | Brain metastasis | A brain metastasis is a cancer that has metastasized (spread) to the brain from another location in the body and is therefore considered a secondary brain tumor. |
1 | list | Blastoma | A cell type cancer that has_material_basis_in abnormally proliferating cells derived_from precursor cells called blast cells. |
1 | list | Malignant mixed tumor | A cell type cancer that has_material_basis_in abnormally proliferating cells derived_from two germinal layers of tissue. |
1 | list | Colpocephaly | A cephalic disorder involving the disproportionate enlargement of the occipital horns of the lateral ventricles |
1 | list | Oxycephaly | A cephalic disorder where the top of the skull is pointed or conical due to premature closure of the coronal suture plus any other suture. |
1 | list | Hereditary cystatin C amyloid angiopathy | A cerebral amyloid angiopathy that has material basis in an autosomal dominant mutation of CST3 on chromosome 20p11.21. |
1 | list | Moyamoya disease | A cerebral arterial disease characterized by constriction of certain arteries at the base of the brain. Blood flow is blocked by the constriction and also by blood clots. |
1 | list | Ataxic cerebral palsy | A cerebral palsy that is caused by damage to the cerebellum, which affects muscle coordination, particularly in the limb. Some individuals suffer from hypotonia, tremors, difficulty with visual and/or auditory processing. |
1 | list | Sandifer syndrome | A childhood disorder characterised by gastrointestinal symptoms and associated neurological features. |
1 | list | Childhood absence epilepsy | A childhood electroclinical syndrome characterized by the occurrence of typical absence seizures starting between the age of four and ten years. |
1 | list | Potocki–Lupski syndrome | A chromosomal duplication syndrome characterized by hypotonia, failure to thrive, mental retardation, pervasive developmental disorders and congenital anomalies that has material basis in duplication of a region of chromosome 17p11.2. |
1 | list | Phimosis | A condition in which there is constriction in the tip of the foreskin resulting in inability to fully retract the foreskin over the glans penis. Causes include balanoposthitis, balanitis xerotica obliterans, and untreated diabetes. |
1 | list | Polymicrogyria | A condition that affects the development of the human brain by multiple small gyri (microgyri) creating excessive folding of the brain leading to an abnormally thick cortex. |
1 | list | Blue balls | A condition that arises during sexual arousal when the sperms or fluid are not ejaculated. |
1 | list | Congenital hepatic fibrosis | A congenital disorder usually inherited in an autosomal recessive pattern. It affects the hepatobiliary system and the kidneys. It is characterized by liver fibrosis, portal hypertension, and renal cysts. |
1 | list | Atopic dermatitis | A dermatitis that is a chronically relapsing inflammatory allergic response located in the skin that causes itching and flaking. |
1 | list | Postencephalitic parkinsonism | A disease believed to be caused by a viral illness that triggers degeneration of the nerve cells in the substantia nigra. Overall, this degeneration leads to clinical parkinsonism. |
1 | list | Spondylocostal dysostosis | A dysostosis that results in abnormal development located in vertebrae or located in ribs. The bones of the spine do not develop properly, which causes them to be misshapen and abnormally joined together. |
1 | list | Claustrophobia | A fear or anxiety of being in small, cramped spaces |
1 | list | Dermatofibrosarcoma protuberans | A fibrosarcoma that is located in the dermis laryer of the skin and that begins as a hard nodule and grows slowly. |
1 | list | Mansonelliasis | A filariasis that involves parasitic infection by the nematodes Mansonella ozzardi or Mansonella perstans, which reside in the skin or body cavities. The nematode is transmitted through the bite of midges and blackflies. |
1 | list | Delusion | A firm and fixed belief in that which is based on inadequate grounding |
1 | list | X-linked dystonia parkinsonism | A focal dystonia characterized by parkinsonism that is frequently accompanied by focal dystonia and progresses to generalized dystonia that has material basis in an SVA retrotransposon insertion in the intron of the TAF1 gene on chromosome Xq13.1. |
1 | list | Epicanthic fold | A fold on upper eye lid |
1 | list | Geographic atrophy | A form of MACULAR DEGENERATION also known as dry macular degeneration marked by occurrence of a well-defined progressive lesion or atrophy in the central part of the RETINA called the MACULA LUTEA. It is distinguishable from WET MACULAR DEG |
1 | list | Kallmann syndrome | A form of hypogonadotropic hypogonadism which is also accompanied by a total lack or partial loss in the sense of smell. The condition affects both males and females and causes a failure in puberty and infertility. |
1 | list | Kenny-Caffey syndrome | A genetic condition characterized by long bone sclerosis and thickening, short stature, and head and eye anomalies. Many affected individuals have hypoparathyroidism with hypocalcemia. |
1 | list | Pythiosis | A granulomatous disease caused by the aquatic organism pythium insidiosum and occurring primarily in horses, cattle, dogs, cats, fishes, and rarely in humans. It is classified into three forms: ocular, cutaneous, and arterial. |
1 | list | Cerebral palsy | A group of disorders affecting the development of movement and posture, often accompanied by disturbances of sensation, perception, cognition, and behavior. It results from damage to the fetal or infant brain. |
1 | list | Metabolic myopathy | A group of rare inherited disorders characterized by a deficiency of enzymes that are involved in metabolic pathways that affect muscles. The disorders are characterized by muscle dysfunction. |
1 | list | Cardiomyopathy | A heart disease and a myopathy that is characterised by deterioration of the function of the heart muscle |
1 | list | Atrial septal defect | A heart septal defect located in in the septum that separates the two atria of the heart. |
1 | list | Congenital hemangioma | A hemangioma present and fully formed at birth. The different types are Rapidly involuting congenital hemangiomas (RICH), Partially involuting congenital hemangioma (PICH) and Non-involuting congenital hemangiomas (NICH). |
1 | list | Fibrolamellar hepatocellular carcinoma | A hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers. |
1 | list | Hip dysplasia (canine) | A hereditary disease of the hip joints in dogs. Signs of the disease may be evident any time after 4 weeks of age. |
1 | list | Proteus syndrome | A human disease characterized by an overgrowth of skin, bones, muscles, fatty tissues, and blood and lymphatic vessels. |
1 | list | Fertile eunuch syndrome | A hypogonadotropic hypogonadism that has_material_basis_in homozygous or compound heterozygous mutation in the LHB gene on chromosome 19q13. |
1 | list | Hypotrichosis with juvenile macular dystrophy | A hypotrichosis that has material basis in a autosomal recessive mutation of CDH3 on chromosome 16q22.1. |
1 | list | Pediculosis corporis | A lice infestation that is a cutaneous condition caused by parasitic infestation of body lice Pediculus humanus corporis, which feed on the human blood. Body lice can spread epidemic typhus, trench fever, and louse-borne relapsing fever. |
1 | list | Cystinosis | A lysosomal storage disease characterized by the abnormal accumulation of cystine in the lysosomes. It follows an autosomal recessive inheritance pattern and has material basis in mutations in the CTNS gene, located on chromosome 17. |
1 | list | Vitelliform macular dystrophy | A macular degeneration that can cause progressive vision loss, it is characterized by the disruption of cells in a small area near the center of the retina, the macula. |
1 | list | Lymphoid leukemia | A malignant lymphocytic neoplasm of B-cell or T-cell lineage involving primarily the bone marrow and the peripheral blood. This category includes precursor or acute lymphoblastic leukemias and chronic leukemias. |
1 | list | Childhood cancer | A malignant tumor that occurs in children. Representative examples include soft tissue and bone sarcomas (e.g. osteosarcoma) and embryonal neoplasms (e.g. hepatoblastoma and rhabdoid tumor). |
1 | list | Ethylene glycol poisoning | A medical condition from too much ethylene glycol |
1 | list | Methylmalonyl-CoA mutase deficiency | A methylmalonic acidemia characterized by accumulation of methylmalonic acid in the blood that is unresponsive to vitamn B12 therapy and that has material basis in mutation in the MUT gene on chromosome 6p12.3. |
1 | list | Familial hemiplegic migraine | A migraine with aura that is characterized by temporary numbness or weakness, often affecting one side of the body (hemiparesis). Additional features of an aura can include difficulty with speech, confusion, and drowsiness. |
1 | list | Leigh syndrome | A mitochondrial metabolism disease characterized by progressive loss of mental and movement abilities. Symptoms usually begin between ages of three months and two years and include loss of appetite, vomiting, irritability and seizure activity. |
1 | list | Opitz G/BBB syndrome | A monogenic disease that is characterized by hypertelorism, hypospadias, and additional midline defects resulting from mutations to the MID1 gene in the X-linked form or from a deletion on chromosome 22q11.2 in the autosomal dominant form. |
1 | list | Hand–Schüller–Christian disease | A multifocal, unisystem form of Langerhans-cell histiocytosis. There is involvement of multiple sites in one organ system, most frequently the bone. Patients are usually young children presenting with multiple destructive bone lesions. |
1 | list | Myostatin-related muscle hypertrophy | A muscle tissue disease characterized by increased muscle bulk and strength that has material basis in homozygous mutation in the MSTN gene on chromosome 2q32.2. |
1 | list | Atypical chronic myeloid leukemia | A myelodysplastic myeloproliferative neoplasm characterized by the principal involvement of the neutrophil series with leukocytosis and multilineage dysplasia. The neoplastic cells do not have a Philadelphia chromosome or the BCR/ABL fusion gene. |
1 | list | Multiple myeloma | A myeloid neoplasm that is located in the plasma cells in bone marrow. |
1 | list | Central nervous system tumor | A neoplasm listed in Medical Subject Headings (MeSH) |
1 | list | B-cell prolymphocytic leukemia | A neoplasm of prolymphocytes affecting the blood, bone marrow, and spleen. It is characterized by prolymphocytes exceeding 55% of the lymphoid cells in the blood and profound splenomegaly. |
1 | list | Schimmelpenning syndrome | A neurocutaneous syndrome with anomalies of the central nervous system, ocular system, skeletal system, cardiovascular system, and genitourinary system. A triad of sebaceous nevi, seizures, and mental retardation. |
1 | list | Pantothenate kinase-associated neurodegeneration | A neurodegeneration with brain iron accumulation that has_material_basis_in autosomal recessive inheritance of mutation in the PANK2 gene on chromosome 20p13. |
1 | list | Jokela type spinal muscular atrophy | A neuromuscular disease |
1 | list | Hamartoma | A non cancerous growth made up of an abnormal mixture of cells and tissues normally found in the area of the body. |
1 | list | Vulvar disease | A non-neoplastic or neoplastic disorder that affects the vulva. Representative examples include infection, Bartholin gland adenoma, and vulvar carcinoma. |
1 | list | Fasciolopsiasis | A parasitic helminthiasis infectious disease that involves parasitic infection of the intestine by Fasciolopsis buski. The symptoms include diarrhea, abdominal pain, fever, ascites, anasarca and intestinal obstruction. |
1 | list | Metagonimiasis | A parasitic helminthiasis infectious disease that involves parasitic infection of the intestine by Metagonimus yokogawai. The symptoms are diarrhea and colicky abdominal pain. The heart and brain can also be infected. |
1 | list | Naegleriasis | A parasitic protozoa infectious disease that involves infection of the central nervous system caused by Naegleria fowleri. The symptoms include headache, nausea, rigidity of the neck muscles, vomiting, delirium, seizures and coma. |
1 | list | Dientamoebiasis | A parasitic protozoa infectious disease that involves infection of the large intestine by a protozoan parasite Dientamoeba fragilis. The symptoms include diarrhea, stomach pain and cramping, loss of appetite and weight, nausea, and fatigue. |
1 | list | Coccidiosis | A parasitic protozoa infectious disease that occurs in the intestinal tract of animals and humans caused by Coccidia protozoa. Immunocompromised persons are at greater risk of developing the infection. |
1 | list | Fibromatosis | A poorly circumscribed neoplasm arising from the soft tissues. It is characterized by the presence of spindle-shaped fibroblasts and an infiltrative growth pattern. |
1 | list | Corticobasal degeneration | A progressive neurodegenerative condition affecting the cerebral cortex and basal ganglia. The disorder is characterized by varying degrees of cognitive and motor impairment. |
1 | list | Persistent Müllerian duct syndrome | A pseudohermaphroditism that is characterized by the persistence of Mullerian duct derivatives (i.e. uterus, cervix, fallopian tubes and upper two thirds of vagina) in a phenotypically and karyotypically male. |
1 | list | Purpura fulminans | A purpura characterized blood spots, bruising and discolouration of the skin resulting from coagulation in small blood vessels within the skin and rapidly leads to skin necrosis and disseminated intravascular coagulation. It is often fatal. |
1 | list | Squamous-cell thyroid carcinoma | A rapidly growing primary carcinoma of the thyroid gland composed of malignant squamous cells. The clinical course is usually aggressive. |
1 | list | DeSanctis–Cacchione syndrome | A rare autosomal recessive inherited syndrome. It is characterized by xeroderma pigmentosum, mental retardation, dwarfism, hypogonadism, and neurologic abnormalities. |
1 | list | Hibernoma | A rare benign slow growing adipose tissue tumor, characterized by the presence of polygonal brown fat cells with multivacuolated and/or granular cytoplasm. The tumor is usually painless and is most often seen in young adults. |
1 | list | Diastematomyelia | A rare congenital abnormality in which the spinal cord is split in half by fibrous or bony tissue. It may present as an isolated phenomenon or in association with spina bifida. |
1 | list | Kasabach–Merritt syndrome | A rare disease usually seen in infants |
1 | list | Hemimegalencephaly | A rare disorder affecting development of one side of the brain |
1 | list | Palatal myoclonus | A rare movement disorder characterized by rhythmic movements of the soft palate. |
1 | list | Pick's disease | A rare neurodegenerative disorder leading to dementia. It is characterized by frontotemporal lobar degeneration with accumulation of tau proteins which form Pick bodies. |
1 | list | Hydroa vacciniforme | A rare skin disorder of unknown etiology affecting children. It is a photodermatitis, characterized by the formation of vesicles and scarring on sun exposed areas. |
1 | list | Meigs' syndrome | A rare syndrome affecting females. It is characterized by pleural effusion, ascites and non-malignant ovarian neoplasm. This syndrome usually follows a benign course. Prognosis is favorable following surgical resection of the ovarian mass. |
1 | list | Winchester syndrome | A rare, autosomal recessive inherited syndrome caused by mutations in the MMP2 gene. It is characterized by the presence of multiple, painless subcutaneous nodules, osteolysis particularly in the hands and feet, osteoporosis, and arthropathy. |
1 | list | Sinonasal undifferentiated carcinoma | A rare, highly aggressive carcinoma that arises from the sinonasal tract. It is characterized by the presence of small to medium size malignant cells. The prognosis is poor. |
1 | list | Progressive muscular atrophy | A rare, milder form of amyotrophic lateral sclerosis. It is characterized by a slowly progressive clinical course. Signs and symptoms include muscle weakness, atrophy, and fasciculation. |
1 | list | Ataxia–telangiectasia | A rare, neurodegenerative, autosomal recessive human disease causing severe disability |
1 | list | Warty dyskeratoma | A rare, usually solitary, benign epithelial tumor of the skin that appears to arise from a hair follicle. It usually develops in the head and neck region as a nodular lesion with a central keratotic plug. |
1 | list | Cystitis glandularis | A reactive inflammatory disorder affecting the bladder. It is characterized by the development of small cysts in the bladder wall. The cysts are lined by metaplastic glandular cells. |
1 | list | Spindle cell sarcoma | A sarcoma that results in cells that are spindle-shaped. They are usually resistant to radiation therapy. |
1 | list | Tetanus | A serious infectious disorder that follows wound contamination by the Gram-positive bacterium Clostridium tetani. The bacteria produce a neurotoxin called tetanospasmin, which causes muscle spasm in the jaw and other anatomic sites. |
1 | list | Necrospermia | A serious masculine fertility issue. |
1 | list | Adenosine deaminase deficiency | A severe combined immunodeficiency that is caused by a defective enzyme, adenosine deaminase (ADA), necessary for the breakdown of purines. Lack of ADA causes accumulation of dATP. |
1 | list | Epileptic spasms | A severe epilepsy syndrome with triad of infantile spasms, an interictal electroencephalogram (EEG) pattern termed hypsarrhythmia, and mental retardation. |
1 | list | Pendular nystagmus | A sinusoidal oscillation, which refers to the waveform of involuntary eye movements that may occur in any direction. |
1 | list | Benign symmetric lipomatosis | A skin condition characterized by extensive symmetric fat deposits in the head, neck, and shoulder girdle area. |
1 | list | T-cell prolymphocytic leukemia | A slow-growing type of leukemia (blood cancer) in which too many lymphocytes are found in the bone marrow and/or blood. The T-cell is specified as the defective cell line. |
1 | list | Alastrim | A smallpox that results in milder infection, located in skin, has material basis in Variola virus. The infection results in formation of lesions. |
1 | list | Unicameral bone cyst | A solitary bone cyst is a benign non-epithelial bone cavity that is asymptomatic and that is found most commonly in the second decade of life by chance. The long bones are most often affected, but cases involving the jaw bone have been reported. |
1 | list | Hyperinsulinemic hypoglycemia | A sporadic or inherited disorder characterized by the focal or diffuse proliferation of the cells of the islets of Langerhans in the pancreas. It results in hyperinsulinemia and hypoglycemia. |
1 | list | Flinders Island spotted fever | A spotted fever that has material basis in Rickettsia honei, which is transmitted by cayenne ticks (Amblyomma cajennense). The infection has symptom mild spotted fever, has symptom eschar and has symptom adenopathy. |
1 | list | Springtime lethargy | A state of fatigue, lowered energy, or depression, associated with the onset of spring |
1 | list | Enterolith | A stone within the digestive tract |
1 | list | Thecoma | A stromal tumor that arises from the ovary and is characterized by the presence of cells that contain lipid and resemble theca cells. The vast majority of cases are benign. |
1 | list | Basal-cell carcinoma | A subtype of basal-cell carcinoma most commonly occurring on the sun-exposed areas of the head and neck |
1 | list | Dupuytren's contracture | A superficial fibromatosis arising from the soft tissue of the palm. It is characterized by the presence of spindle-shaped fibroblasts, and an infiltrative growth pattern. It predominantly affects adult males. |
1 | list | Miller–Dieker syndrome | A syndrome characterized by classical lissencephaly and distinct facial features. Visible and submicroscopic deletions of 17p13.3, including the LIS1 gene, are found in almost 100% of patients. |
1 | list | Goldberg–Shprintzen syndrome | A syndrome characterized by intellectual disability, specific facial gestalt and Hirschsprung's disease (HSCR). It has material basis in homozygous mutation in the KIAA1279 gene on chromosome 10q21.1. |
1 | list | Perlman syndrome | A syndrome characterized by polyhydramnios with neonatal macrosomia, nephromegaly, distinctive facial appearance, renal dysplasia, nephroblastomatosis, and predisposition to Wilms tumor. It shows similarities to Beckwith-Wiedemann syndrome. |
1 | list | Parinaud's oculoglandular syndrome | A syndrome of the eye |
1 | list | Gorham's disease | A syndrome that is characterized by bone loss (osteolysis) which is often associated with swelling or abnormal blood vessel growth (angiomatous proliferation). Bone loss can occur in just one bone or spread to soft tissue and adjacent bones. |
1 | list | Goldenhar syndrome | A syndrome that is characterized by incomplete development of the ear, nose, soft palate, lip, and mandible. It is associated with anomalous development of the first branchial arch and second branchial arch. |
1 | list | IgG4-related disease | A systemic fibroinflammatory disease, associated with elevated serum IgG4 levels in about 60% of cases |
1 | list | Gumma (pathology) | A tertiary syphilis that is characterized by granulomatous lesions, called gummas, which are characterized by a center of necrotic tissue with a rubbery texture. They form in the liver, bones, and testes but may affect any organ. |
1 | list | Thymoma | A thymus cancer that derives from epithelial cells located in the thymus. The tumor cells in a thymoma look similar to the normal cells of the thymus, grow slowly, and rarely spread beyond the thymus. |
1 | list | Thymic carcinoma | A thymus cancer that derives from epithelial cells. The tumor cells in a thymic carcinoma look very different from the normal cells of the thymus, grow more quickly, and have usually spread to other parts of the body when the cancer is found. |
1 | list | Tricuspid insufficiency | A tricuspid valve disease that is characterized by failure of the heart's tricuspid valve to close properly during systole. As a result, with each heart beat, blood is pumped out from the right side of the heart in the opposite direction to normal. |
1 | list | Sensorineural hearing loss | A type of Hearing Loss |
1 | list | Mesothelioma | A type of cancer that develops from the thin layer of tissue that covers many of the internal organs (known as the mesothelium) |
1 | list | Lupus erythematosus panniculitis | A type of lupus erythematosus characterized by deep dermal or subcutaneous nodules, most often on the head, face, or upper arms. It is generally chronic and occurs most often in women between the ages of 20 and 45. |
1 | list | Myopericytoma | A usually slow growing, subcutaneous nodular neoplasm arising from myopericytes. It is composed of myoid cells arranged in a perivascular growth pattern. The vast majority of cases have a benign clinical course. |
1 | list | Complex post-traumatic stress disorder | A variant of Posttraumatic Stress Disorder typically caused by ongoing abuse or stressful environment |
1 | list | Diffuse idiopathic pulmonary neuroendocrine cell hyperplasia | A very rare condition characterized by generalized proliferation of pulmonary neuroendocrine cells. It manifests as progressive cough and dyspnea. It is considered a precursor for pulmonary carcinoid tumor. |
1 | list | Lacunar amnesia | AMNESIA LACUNAR |
1 | list | Atelosteogenesis type I | AO1. AOI. Atelosteogenesis type 1. Giant cell chondrodysplasia. Spondylo-humero-femoral dysplasia |
1 | list | Pneumothorax | Abnormal collection of air in the pleural space that causes an uncoupling of the lung from the chest wall |
1 | list | Stenosis | Abnormal narrowing of a blood vessel or other tubular organ or structure. It is also sometimes called a stricture. |
1 | list | Bacterial vaginosis | Abnormal vaginal bacteria population |
1 | list | Hypotonia | Abnormally low muscle tone |
1 | list | Trichiasis | Abnormally positioned eyelashes |
1 | list | Accelerated idioventricular rhythm | Accelerated idioventricular rhythm is a ventricular rhythm with a rate of between 40 and 120 beats per minute. |
1 | list | Aceruloplasminemia | Aceruloplasminemia is an adult-onset disorder of neurodegeneration with brain iron accumulation (NBIA; see this term) characterized by anemia, retinal degeneration, diabetes and various neurological symptoms |
1 | list | Achard–Thiers syndrome | Achard–Thiers syndrome combines the features of adrenogenital syndrome and Cushing syndrome. It occurs mainly in post-menopausal women |
1 | list | Acquired C1 esterase inhibitor deficiency | Acquired angioedema (AAE) is characterized by the occurrence of transitory and recurrent subcutaneous and/or submucosal edemas resulting in swelling and/or abdominal pain due to an acquired C1 inhibitor (C1-INH) deficiency |
1 | list | Barraquer–Simons syndrome | Acquired partial lipodystrophy, or Barraquer-Simons syndrome, is characterised by the association of lipoatrophy of the upper part of the body and lipohypertrophy of the thighs |
1 | list | Acromicric dysplasia | Acromicric dysplasia is a rare bone dysplasia characterized by short stature, short hands and feet, mild facial dysmorphism, and characteristic X-ray abnormalities of the hands |
1 | list | Pouchitis | Acute inflammation in the intestinal mucosa of the continent ileal reservoir (or pouch) in patients who have undergone ileostomy and restorative proctocolectomy (proctocolectomy, restorative) |
1 | list | Adult polyglucosan body disease | Adult polyglucosan body disease (APBD) is a glycogen storage disease of adults characterized by progressive upper and lower motor neuron dysfunction, progressive neurogenic bladder and cognitive difficulties that can lead to dementia |
1 | list | Sporadic late-onset nemaline myopathy | Adult-onset nemaline myopathy is a rapidly progressive type of nemaline myopathy (NM; see this term) characterized by a very late onset |
1 | list | Alcohol and pregnancy | Alcohol use during pregnancy |
1 | list | Tree nut allergy | Allergic reaction to tree nuts that is triggered by the immune system |
1 | list | Alpha-thalassemia | Alpha thalassemia is a thalassemia involving the genes HBA1and HBA2 hemoglobin genes |
1 | list | Early-onset Alzheimer's disease | Alzheimer's disease developing before the age of 65 |
1 | list | Lori and George Schappell | American singer |
1 | list | Aminoacylase 1 deficiency | Aminoacylase 1 deficiency (ACY1D) is an inborn error of metabolism marked by a characteristic pattern of urinary N-acetyl amino acid excretion and neurologic symptoms |
1 | list | Sakati–Nyhan–Tisdale syndrome | An acrocephalosyndactylia characterized by abnormalities in the bones of the legs, congenital heart defects and craniofacial defects and craniosynostosis. The patients suffer from cyanosis and other respiratory and breathing infections. |
1 | list | Acrodermatitis chronica atrophicans | An acrodermatitis characterized by a chronically progressive course, leading to widespread atrophy of the skin. It is a clinical manifestation of Lyme borreliosis. |
1 | list | Acute myelomonocytic leukemia | An acute leukemia characterized by the proliferation of both neutrophil and monocyte precursors. (WHO, 2001) |
1 | list | Acute myeloblastic leukemia with maturation | An acute myeloid leukemia (AML) characterized by blasts with evidence of maturation to more mature neutrophils. (WHO, 2001) |
1 | list | Acute myeloblastic leukemia without maturation | An acute myeloid leukemia (AML) characterized by blasts without evidence of maturation to more mature neutrophils. (WHO, 2001) |
1 | list | Desmoplastic small-round-cell tumor | An aggressive and rare cancer |
1 | list | Adenine phosphoribosyltransferase deficiency | An amino acid metabolic disorder characterized by the formation 2,8-dihydroxyadenine stones and renal failure secondary to intratubular crystalline precipitation. It has an autosomal recessive inheritance pattern. |
1 | list | Hypermethioninemia | An amino acid metabolic disorder that involves an excess of the amino acid methionine, in the blood. This condition can occur when methionine is not broken down properly in the body. |
1 | list | Rheumatoid arthritis | An arthritis that is an autoimmune disease which attacks healthy cells and tissue located in joint. |
1 | list | Autoimmune polyendocrine syndrome type 2 | An autoimmune polyendocrine syndrome that is characterized by abnormal functioning of the immune system that causes auto-reactivity against endocrine organs. It is more heterogeneous and has not been linked to one gene. |
1 | list | Deficiency of the interleukin-1–receptor antagonist | An autoinflammatory disease caused by mutations in the IL1RN gene, which encodes the IL1 receptor antagonist. It presents in infancy, and is characterized by systemic inflammation, pustular rash, bone pain, sterile osteitis, and periostitis. |
1 | list | Neuroblastoma | An autonomic nervous system neoplasm that is derived from immature nerve cells. |
1 | list | Blau syndrome | An autosomal dominant disease characterized by familial granulomatous arthritis, uveitis and skin granulomas. It has material basis in mutations in the NOD2/CARD15 genes. |
1 | list | Timothy syndrome | An autosomal dominant disease that is characterized by cardiac, hand/foot, facial, and neurodevelopmental features. The two forms are type 1 (classic) and type 2, a rare form that has material basis in mutations in a transcript variant of CACNA1C. |
1 | list | Facioscapulohumeral muscular dystrophy | An autosomal dominant disorder affecting the skeletal muscles of the face, scapula, and upper arm. Patients present with muscle weakness in these anatomic areas. The muscle weakness eventually spreads to other skeletal muscles as well. |
1 | list | Helsmoortel-Van der Aa syndrome | An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of ADNP on chromosome 20q13.13. |
1 | list | Xia-Gibbs syndrome | An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of AHDC1 on chromosome 1p36.1-p35.3. |
1 | list | White Sutton syndrome | An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of POGZ on chromosome 1q21.3. |
1 | list | Vici syndrome | An autosomal recessive disease characterized by callosal agenesis, cataracts, cardiomyopathy, combined immunodeficiency and hypopigmentation. It has material basis in mutation in the EPG5 gene on chromosome 18q12.3. |
1 | list | Oliver–McFarlane syndrome | An autosomal recessive disease characterized by trichomegaly, severe chorioretinal atrophy and multiple pituitary hormone deficiencies that has material basis in homozygous or compound heterozygous mutation in PNPLA6 on 19p13.2. |
1 | list | Hereditary pyropoikilocytosis | An autosomal recessive inherited severe hemolytic anemia. It is a subtype of hereditary elliptocytosis and is characterized by partial spectrin deficiency. |
1 | list | Hypocholesterolemia | An decreased concentration of cholesterol in the blood. |
1 | list | Acute disseminated encephalomyelitis | An encephalomyelitis characterized by inflammation located in brain and located in spinal cord that damages myelin. It usually occurs after viral infection, but also following vaccination, bacterial or parasitic infection. |
1 | list | Otitis externa | An external ear disease that involves inflammation of the outer ear and ear canal. It can be caused by active bacterial or fungal infections. |
1 | list | Hyperdontia | An extra tooth, erupted or unerupted, resembling or unlike the other teeth in the group to which it belongs. Its presence may cause malposition of adjacent teeth or prevent their eruption. |
1 | list | Suberosis | An extrinsic allergic alveolitis caused by inhalation of cork dust containing the antigens produced by the fungus Penicillium glabrum. The symptoms include dyspnea, wheezing cough, fever and asthenia. |
1 | list | Farmer's lung | An extrinsic allergic alveolitis which is induced by the inhalation of spores (Aspergillus sp and thermophilic actinomycetes) in dust from moldy hay or straw. It is characterized by sudden onset, fever, cough, expectoration, and breathlessness. |
1 | list | WHIM syndrome | An immunodeficiency disease characterized by neutropenia, hypogammaglobulinemia, and extensive human papillomavirus (HPV) infection. It has material basis in heterozygous mutation in the CXCR4 gene on chromosome 2q22. |
1 | list | Balanitis | An infectious or non-infectious inflammatory process that affects the glans penis. Symptoms include redness and pain of the glans penis and foreskin and discharge. |
1 | list | Enterocolitis | An inflammatory process affecting the small intestine and colon. Causes include viruses, bacteria, radiation, and antibiotics use. |
1 | list | Type IV hypersensitivity | An inflammatory response driven by T cell recognition of processed soluble or cell-associated antigens leading to cytokine release and leukocyte activation. |
1 | list | Type II hypersensitivity | An inflammatory response resulting in cell death or dysfunction mediated by activation of the classical complement pathway or induction of effector cell phagocytosis, cytolysis mechanisms via complement or Fc receptors following the binding of antibo |
1 | list | Hypersensitivity | An inflammatory response to an exogenous environmental antigen or an endogenous antigen initiated by the adaptive immune system. |
1 | list | Dyslipidemia | An inherited acute metabolic disorder that involves the creation and degradation of lipids. |
1 | list | Haemophilia B | An inherited blood coagulation disease that has material basis in Factor IX deficiency, which makes coagulation much more prolonged. The disease is inherited as an X-linked recessive trait. |
1 | list | Porphyria | An inherited metabolic disorder that involves certain enzymes in the heme bio-synthetic pathway resulting in the overproduction and accumulation of porphyrins. |
1 | list | Retiform hemangioendothelioma | An intermediate, locally aggressive and rarely metastasizing blood vessel neoplasm. It is characterized by the presence of hobnail endothelial cells and formation of arborizing vascular channels. |
1 | list | Endovascular papillary hemangioendothelioma | An intermediate, rarely metastasizing blood vessel neoplasm. It is characterized by the presence of lymphatic-like vascular channels and papillary endothelial proliferation. |
1 | list | Keloid | An irregularly shaped, elevated mark on the skin caused by deposits of excessive amounts of collagen during wound healing. It extends beyond the original boundaries of the wound and may enlarge progressively. |
1 | list | Orofaciodigital syndrome 1 | An orofaciodigital syndrome characterized_by polycystic kidney disease and variable involvement of the central nervous system and has_material_basis_in X-linked inheritance of the OFD1 gene. |
1 | list | Multiple epiphyseal dysplasia | An osteochondrodysplasia that has material basis in defective cartilage mineralization into bone which results in irregular ossification centers of the located in hip or located in knee. The disease has symptom fatigue, has symptom joint pain. |
1 | list | Ovine pulmonary adenocarcinoma | Animal disease |
1 | list | Annular lichen planus | Annular lichen planus (LP) is a rare variant of cutaneous lichen planus (see this term) characterized by the development of annular lesions |
1 | list | Oroantral fistula | Antrumperforation |
1 | list | Primarily obsessional obsessive compulsive disorder | Anxiety disorder |
1 | list | Temporomandibular joint pathology | Any condition affecting the anatomic and functional characteristics of the temporomandibular joint |
1 | list | Primary tumors of the heart | Any of the forms of heart neoplasm that have a rare incidence |
1 | list | Odontogenic tumor | Any of the forms of odontogenic neoplasm |
1 | list | Parathyroid neoplasm | Any of the forms of tumor of parathyroid gland that have a rare incidence |
1 | list | Reticulocytopenia | Aplastic crisis |
1 | list | Corneal ulcer | Area of epithelial tissue loss from corneal surface; associated with inflammatory cells in the cornea and anterior chamber |
1 | list | Astrocytoma | Astrocytomas are a type of cancer of the brain. They originate in a particular kind of glial cells, star-shaped brain cells in the cerebrum called astrocytes. |
1 | list | Atrophic lichen planus | Atrophic lichen planus (LP) is a rare variant of cutaneous lichen planus (see this term) characterized by the development of pale papules or plaques with an atrophic center |
1 | list | Autoimmune disease in women | Autoimmune diseases in women and the unique characteristics and differences between genders |
1 | list | Hypogammaglobulinemia | B cell deficiency that is caused by a reduction in all types of gamma globulins |
1 | list | Waldenström's macroglobulinemia | B-cell lymphocytic neoplasm characterized by an uncontrolled increase of B-cells |
1 | list | Mantle cell lymphoma | B-cell lymphocytic neoplasm due to CD5 positive antigen-naive pregerminal center B-cell within the mantle zone that surrounds normal germinal center follicles |
1 | list | Diffuse large B-cell lymphoma | B-cell lymphoma that is a cancer of B cells presenting as an aggressive tumour which can arise in virtually any part of the body |
1 | list | Marginal zone B-cell lymphoma | B-cell lymphoma that is characterized by initial formation in the marginal zones of lymph tissue |
1 | list | Barber–Say syndrome | Barber Say syndrome (BSS) is a rare ectodermal dysplasia with neonatal onset characterized by congenital generalized hypertrichosis, atrophic skin, ectropion and macrostomia |
1 | list | Bazex–Dupré–Christol syndrome | Bazex-DuprC)-Christol syndrome is a rare genodermatosis with a predisposition to early-onset basal cell carcinomas |
1 | list | Compulsive hoarding | Behavioral pattern characterized by compulsive acquisition and storing of goods |
1 | list | Benign paroxysmal torticollis | Benign paroxysmal torticollis of infancy (BPTI) is a rare functional disorder characterised by recurrent episodes of torticollic posturing of the head (inclination or tilting of the head to one side) in healthy children |
1 | list | Lipoma | Benign tumor made of fat tissue |
1 | list | Pashayan syndrome | Blepharonasofacial syndrome is a rare otorhinolaryngological malformation syndrome characterized by a distinctive mask-like facial dysmorphism, lacrimal duct obstruction, extrapyramidal features, digital malformations and intellectual disability |
1 | list | Couvelaire uterus | Blood from detached placental site'which enter into uterine musculature and peritoneal cavity |
1 | list | Blue diaper syndrome | Blue Diaper syndrome is a hereditary metabolic disorder characterised by hypercalcaemia with nephrocalcinosis and indicanuria |
1 | list | Blue rubber bleb nevus syndrome | Blue rubber bleb nevus (BRBNS) is a rare vascular malformation disorder with cutaneous and visceral lesions frequently associated with serious, potentially fatal bleeding and anemia |
1 | list | Cytokine release syndrome | Bodily reaction |
1 | list | Bohring–Opitz syndrome | Bohring-Opitz Syndrome is an extremely rare genetic syndrome.This syndrome is diagnosed by genetic testing and is a mutation in the ASXL1 gene. |
1 | list | BDSM | Bondage and Discipline, Dominance and Submission, Sadism and Masochism |
1 | list | Biemond syndrome | Brachydactyly-nystagmus-cerebellar ataxia syndrome is characterized by brachydactyly, nystagmus and cerebellar ataxia. Intellectual deficit and strabismus are also reported in some patients. |
1 | list | Baggio–Yoshinari syndrome | Brazilian tick-borne disease |
1 | list | Anal fissure | Break or tear in the skin of the anal canal |
1 | list | Judge Rinder | British court show |
1 | list | Bronchogenic cyst | Bronchogenic cysts (BCs) are congenital malformations resulting from abnormal budding of the foregut and are most commonly found in the mediastinum |
1 | list | Tendinopathy | Bruised tendon |
1 | list | Black eye | Brusing injury to the face |
1 | list | Bullous impetigo | Bullous impetigo |
1 | list | Bullous lichen planus | Bullous lichen planus is a variant of rare lichen planus (see this term) characterized by the development of vesico-bullous lesions |
1 | list | CHILD syndrome | CHILD syndrome (Congenital Hemidysplasia with Ichthyosiform nevus and Limb Defects, CS) is an X-linked dominant genodermatosis characterized by unilateral inflammatory and scaling skin lesions with ipsilateral visceral and limb anomalies |
1 | list | Zunich–Kaye syndrome | CHIME syndrome is a rare ectodermal dysplasia syndrome characterized by ocular colobomas, cardiac defects, ichthyosiform dermatosis, intellectual disability, conductive hearing loss and epilepsy |
1 | list | CLOVES syndrome | CLOVE syndrome is characterized by Congenital Lipomatous Overgrowth, progressive, complex and mixed truncal Vascular malformations, and Epidermal nevi |
1 | list | Krista and Tatiana Hogan | Canadian craniopagus conjoined twins |
1 | list | Idiopathic multicentric Castleman disease | Castleman disease characterized by systemic inflammatory symptoms, polyclonal lymphoproliferation, cytopenias, and multiple organ system dysfunction caused by a cytokine storm often including interleukin-6 |
1 | list | Cataract-microcornea syndrome | Cataract-microcornea syndrome is characterized by the association of congenital cataract and microcornea without any other systemic anomaly or dysmorphism |
1 | list | Borderline intellectual functioning | Category of intelligence |
1 | list | Catel–Manzke syndrome | Catel-Manzke syndrome is a rare bone disease characterized by bilateral hyperphalangy and clinodactyly of the index finger typically in association with Pierre Robin sequence (see this term) comprising micrognathia, cleft palate and glossoptosis |
1 | list | Pascual-Castroviejo syndrome | Cerebro-facio-thoracic dysplasia or Pascual-Castroviejo syndrome type 1 is a rare syndrome characterized by facial dysmorphism, intellectual deficit and costovertebral abnormalities |
1 | list | Perineal tear | Childbirth related injury |
1 | list | Lamaze technique | Childbirth technique |
1 | list | Foot binding | Chinese custom of applying tight binding to the feet of young girls to modify the shape and size of their feet as a status symbol and mark of beauty, practised from 10th to early 20th centuries |
1 | list | Neonatal-onset multisystem inflammatory disease | Chronic Infantile Neurological, Cutaneous, and Articular (CINCA) syndrome is characterised by skin rash, joint involvement, chronic meningitis with granulocytes and, in some cases, sensorineural hearing loss and ocular signs |
1 | list | Leprosy | Chronic infection caused by bacteria Mycobacteria lepræ and lepromatosis |
1 | list | Ho–Kaufman–Mcalister syndrome | Cleft palate, micrognathia, Wormian bones, congenital heart disease, dislocated hips, absent tibiae, bowed fibulae, preaxial polydactyly of the feet |
1 | list | Adipsia | Clinically significant lack of expression of thirst. |
1 | list | Cohen syndrome | Cohen syndrome (CS) is a rare genetic developmental disorder characterized by microcephaly, characteristic facial features, hypotonia, non-progressive intellectual deficit, myopia and retinal dystrophy, neutropenia and truncal obesity |
1 | list | Cold agglutinin disease | Cold agglutinin disease is a type of autoimmune hemolytic anemia (see this term) defined by the presence of cold autoantibodies (autoantibodies which are active at temperatures below 30B0C) |
1 | list | Cardiac tamponade | Compression of the heart due to excessive accumulation of fluid in the pericardium (sac in which the heart is enclosed) |
1 | list | Retrograde ejaculation | Condition is which semen is redirected to the urinary bladder rather than ejaculated |
1 | list | Congenital tufting enteropathy | Congenital Tufting Enteropathy is a rare congenital enteropathy presenting with early-onset severe and intractable diarrhea that leads to irreversible intestinal failure |
1 | list | Analbuminaemia | Congenital analbuminemia (CAA) is characterized by the absence or dramatic reduction of circulating human serum albumin (HSA) |
1 | list | Webbed neck | Congenital anatomic variant. |
1 | list | Cubitus valgus | Congenital deformity |
1 | list | Pectus carinatum | Congenital deformity of the chest |
1 | list | Crouzon syndrome | Congenital disorder of the skull and face |
1 | list | Congenital dyserythropoietic anemia type I | Congenital dyserythropoietic anemiatype I (CDA I) is a hematologic disorder of erythropoiesis characterized by moderate to severe macrocytic anemia occasionally associated with limb or nail deformities and scoliosis |
1 | list | Congenital lobar emphysema | Congenital lobar emphysema (CLE) is a respiratory abnormality characterized by respiratory distress due to hyperinflation of one or more affected lobes of the lung |
1 | list | Sucrose intolerance | Congenital sucrase-isomaltase deficiency (CSID) is a carbohydrate intolerance disorder characterised by malabsorption of oligosaccharides and disaccharides |
1 | list | Urophagia | Consumption of urine |
1 | list | Hunan hand syndrome | Contact dermatitis associated with capsaicin |
1 | list | Cooks syndrome | Cooks syndrome is a malformation syndrome affecting the apical structures of digits and presenting with hypo/aplasia of nails and distal phalanges. More than half of digits are usually involved and the thumbs may appear digitalized. |
1 | list | Corticobasal syndrome | Corticobasal syndrome (CBS) is a rare neurodegenerative disease characterized by multifaceted motor system dysfunctions and cognitive defects such as asymmetric rigidity, bradykinesia, limb apraxia, and visuospatial dysfunction |
1 | list | Cranio-lenticulo-sutural dysplasia | Craniolenticulosutural dysplasia (CLSD), also known as Boyadjiev-Jabs syndrome, is characterized by the specific association of large and late-closing fontanels, hypertelorism, early-onset cataract and mild generalized skeletal dysplasia |
1 | list | Upskirt | Criminal offence in certain jurisdictions |
1 | list | Melancholic depression | DSM-IV subtype of clinical depression |
1 | list | Muehrcke's nails | Dark horizontal lines on fingernails |
1 | list | Emberger syndrome | Deafness - lymphedema - leukemia is a very rare, serious syndromic genetic disorder characterized by primary lymphedema, immunodeficiency, and hematological disorders |
1 | list | Beau's lines | Deep horizontal ridges in fingernails |
1 | list | 2q37 monosomy | Deletion 2q37 or monosomy 2q37 is a chromosomal anomaly involving deletion of chromosome band 2q37 and manifests as three major clinical findings: developmental delay, skeletal malformations and facial dysmorphism |
1 | list | Idiopathic osteosclerosis | Dental condition |
1 | list | Paresthesia | Dermal sensation |
1 | list | Atrophodermia vermiculata | Dermatological condition |
1 | list | Tinea faciei | Dermatophytosis |
1 | list | Desmosterolosis | Desmosterolosis is a very rare sterol biosynthesis disorder characterized by multiple congenital anomalies, failure to thrive, and intellectual disability, with elevated levels of desmosterol |
1 | list | Complex regional pain syndrome | Devastating neuropathic-orthopedic disorder; being both Type I (RSD) & Type II (CRPS) |
1 | list | Giacomo and Giovanni Battista Tocci | Dicephalic conjoined twins |
1 | list | Diencephalic syndrome | Diencephalic syndrome (DS) is a rare condition characterized by profound emaciation and failure to thrive (with normal caloric intake and normal linear growth), hyperalertness, hyperkinesias and euphoria, in the presence of hypothalamic tumors |
1 | list | Obstructed defecation | Difficult defecation. |
1 | list | Megacystis (fetal) | Dilatation of the bladder |
1 | list | Q fever | Disease caused by infection with Coxiella burnetiiq |
1 | list | Scleritis | Disease of human eye |
1 | list | Heterochromia iridum | Disease resulting from genetics or injury causing someone to have different colored eyes |
1 | list | Root rot | Disease that causes plant roots to rot |
1 | list | Fetal warfarin syndrome | Disorder of the embryo caused by maternal warfarin administration |
1 | list | Disorders of calcium metabolism | Disorders in the processing of calcium in the body: its absorption, transport, storage, and utilization |
1 | list | Primary autonomic failure | Disorders of the autonomic nervous system occurring as a primary condition. Manifestations can involve any or all body systems but commonly affect the blood pressure and heart rate. |
1 | list | Distal trisomy 10q | Distal trisomy of the long arm of chromosome 10 (10q) is characterized by pre- and postnatal growth retardation, a pattern of specific facial features, hypotonia, and developmental and psychomotor delay |
1 | list | Homesickness | Distress caused by being away from home |
1 | list | Dopamine beta hydroxylase deficiency | Dopamine beta-hydroxylase deficiency is an extremely rare genetic metabolic disorder characterized by autonomic dysregulation leading mainly to orthostatic hypotension |
1 | list | Doping in Russia | Doping in Russia |
1 | list | Drug-induced autoimmune hemolytic anemia | Drug-induced autoimmune hemolytic anemia is a type of autoimmune hemolytic anemia (AIHA; see this term) that occurs as a reaction to therapeutic drugs, and can be due to various mechanisms |
1 | list | Drug-induced QT prolongation | Drugs which induce QT segment prolongation |
1 | list | Duchenne muscular dystrophy | Duchenne muscular dystrophy (DMD) is a neuromuscular disease characterized by rapidly progressive muscle weakness and wasting due to degeneration of skeletal, smooth and cardiac muscle |
1 | list | VLDLR-associated cerebellar hypoplasia | Dysequilibrium syndrome (DES) is a non-progressive cerebellar disorder characterized by ataxia associated with an intellectual disability, delayed ambulation and cerebellar hypoplasia |
1 | list | Anophthalmia | Día mundial de la microftalmia 14 de junio |
1 | list | Eales disease | Eales disease (ED) is an idiopathic, inflammatory retinal venous occlusive disease characterized by 3 stages: vasculitis, occlusion and retinal neovascularization, leading to recurrent vitreous hemorrhages and vision loss |
1 | list | Avoidant/restrictive food intake disorder | Eating disorder |
1 | list | Pagophagia | Eating disorder characterized by the compulsive consumption of ice or iced drinks |
1 | list | Hallucinogen persisting perception disorder | Effects mental disorder |
1 | list | Eiken syndrome | Eiken syndrome is a rare familial skeletal dysplasia characterized by multiple epiphyseal dysplasia, with extremely retarded ossification. It has been described in 6 members of a unique consanguineous family. |
1 | list | Ketosis | Energy production using stored body fats as fuel when carbohydrates are not available |
1 | list | Wetlook | Enjoying getting wet while being clothed or fully clothed (with shoes...), no swimsuit nor waterwear of any kind (swimming trunks/ bikini's, wetsuit...) |
1 | list | Yokkaichi asthma | Epidemic of asthma caused by air pollution in Japan |
1 | list | Skin fragility syndrome | Epidermolysis bullosa simplex due to plakophilin deficiency (EBS-PD) is a suprabasal subtype of epidermolysis bullosa simplex (EBS, see this term) characterized by generalized superficial erosions and less commonly blistering |
1 | list | Epidermolysis bullosa simplex with mottled pigmentation | Epidermolysis bullosa simplex with mottled pigmentation (EBS-MP) is a basal subtype of epidermolysis bullosa simplex (EBS, see this term) characterized by generalized blistering with mottled or reticulate brown pigmentation |
1 | list | Esotropia | Esotropia is a strabismus in which the eye turns inward toward the nose |
1 | list | Photokeratitis | Eyes with no protection to the UV rays |
1 | list | Prosopagnosia | Face blindness - the inability to recognize familiar faces |
1 | list | Dysfibrinogenemia | Familial dysfibrinogenemia is a coagulation disorder characterized by a bleeding tendency due to a functional anomaly of circulating fibrinogen |
1 | list | Congenital hypofibrinogenemia | Familial hypofibrinogenemia is a coagulation disorder characterized by mild bleeding symptoms following trauma or surgery due to a reduced plasma fibrinogen concentration |
1 | list | McGillivray syndrome | Familial scaphocephaly syndrome, McGillivray type is a rare newly described craniosynostosis (see this term) syndrome characterized by scaphocephaly, macrocephaly, severe maxillary retrusion, and mild intellectual disability |
1 | list | Thyroid dyshormonogenesis | Familial thyroid dyshormonogenesis is a type of primary congenital hypothyroidism (see this term), a permanent thyroid hormone deficiency that is present from birth, which results from inborn errors of thyroid hormone synthesis |
1 | list | Glycogen storage disease type XI | Fanconi-Bickel glycogenosis (FBG) is a rare glycogen storage disease characterized by hepatorenal glycogen accumulation, severe renal tubular dysfunction and impaired glucose and galactose metabolism |
1 | list | Rabies | Fatal viral disease |
1 | list | Ghon focus | Feature of Tuberculosis seen in Chest X-Ray |
1 | list | Derealization | Feeling as though the external world is not real |
1 | list | Feline spongiform encephalopathy | Feline brain disease |
1 | list | Facial femoral syndrome | Femoral-facial syndrome is characterized by predominant femoral hypoplasia (bilateral or unilateral) and unusual facies |
1 | list | Lucio and Simplicio Godina | Filipino conjoined twins |
1 | list | Floating–Harbor syndrome | Floating-Harbor syndrome is a genetic developmental disorder characterized by facial dysmorphism, short stature with delayed bone age, and expressive language delay |
1 | list | Athlete's foot | Foot disease |
1 | list | Fountain syndrome | Fountain syndrome is an extremely rare multi-systemic genetic disorder characterized by intellectual disability, deafness, skeletal abnormalities and coarse facial features |
1 | list | Ulna fracture | Fractures of the larger bone of the forearm. |
1 | list | Fragile X-associated tremor/ataxia syndrome | Fragile X-associated tremor/ataxia syndrome (FXTAS) is a rare neurodegenerative disorder characterized by adult-onset progressive intention tremor and gait ataxia |
1 | list | Fraser syndrome | Fraser syndrome is a rare clinical entity including as main characteristics cryptophthalmos and syndactyly |
1 | list | Frontal fibrosing alopecia | Frontal fibrosing alopecia (FFA) is a rare variant of lichen planopilaris (see this term) characterized by symmetrical, progressive, band-like anterior hair loss of the scalp |
1 | list | GAPO syndrome | GAPO syndrome is a multiple congenital anomalies (MCA) syndrome involving connective tissue characterized by Growth retardation, Alopecia, Pseudoanodontia and Ocular manifestations |
1 | list | GM2-gangliosidosis, AB variant | GM2 gangliosidosis, AB variant is an extremely rare, severe genetic disorder characterized by progressive neurological decline due to ganglioside activator deficiency |
1 | list | Tay–Sachs disease | GM2 gangliosidosis, variant B or Tay-Sachs disease is marked by accumulation of G2 gangliosides due to hexosaminidase A deficiency |
1 | list | Glutathionuria | Gamma-glutamyl transpeptidase deficiency is characterized by increased glutathione concentration in the plasma and urine |
1 | list | Townes–Brocks syndrome | Genetic Disorder |
1 | list | Rett syndrome | Genetic brain disorder |
1 | list | Freemartin | Genetic condition of female mammals |
1 | list | Prader–Willi syndrome | Genetic disorder |
1 | list | Familial hyperaldosteronism | Genetic hyperaldosteronism |
1 | list | Genetics of infertility | Genetic infertility |
1 | list | Genetics of obesity | Genetic obesity |
1 | list | Ghosal hematodiaphyseal dysplasia | Ghosal hematodiaphyseal dysplasia syndrome (GHDD) is a rare disorder characterized by increased bone density (predominantly diaphyseal) and aregenerative corticosteroid-sensitive anemia |
1 | list | Glucose-galactose malabsorption | Glucose-galactose malabsorption (GGM) is a very rare, potentially lethal, genetic metabolic disease characterized by impaired glucose-galactose absorption resulting in severe watery diarrhea and dehydration with onset inthe neonatal period |
1 | list | Glutaric aciduria type 1 | Glutaryl-CoA dehydrogenase (GCDH) deficiency (GDD) is an autosomal recessive neurometabolic disorder clinically characterized by encephalopathic crises resulting in striatal injury and a severe dystonic dyskinetic movement disorder |
1 | list | Glycogen storage disease type VI | Glycogen storage disease |
1 | list | Griscelli syndrome type 3 | Griscelli syndrome characterized by isolated silvery gray sheen of the hair and hypopigmentation of the skin that has material basis in mutation in the MLPH or MYO5A genes |
1 | list | HCV in children and pregnancy | HCV and pregnancy |
1 | list | Long-term nonprogressor | HIV-infected individual who does not progress to immune deficiency |
1 | list | HIV/AIDS in Africa | HIV/AIDS in Africa |
1 | list | Rangeliosis | Haemorrhagic disease affecting young dogs and canides, caused by Rangelia vitalii |
1 | list | Haim–Munk syndrome | Haim-Munk syndrome (HMS) is characterized by palmoplantar hyperkeratosis, severe early-onset periodontitis, onychogryposis, pes planus, arachnodactyly and acroosteolysis |
1 | list | Congenital self-healing reticulohistiocytosis | Hashimoto-Pritzker histiocytosis (HPH) is a variant of Langerhans cell histiocytosis (see this term) characterized by multiple disseminated skin lesions (firm, red-brown, painless papulo-nodules) |
1 | list | Ventilator-associated lung injury | Health |
1 | list | Overmedication | Health care issue |
1 | list | Obesity in Sweden | Health issue in Sweden |
1 | list | Acute radiation syndrome | Health problems caused by exposure to very high levels of ionizing radiation |
1 | list | Post-lingual deafness | Hearing disease |
1 | list | Dysacusis | Hearing impairment and discomfort due a distorted perception of sound |
1 | list | Hepatocellular adenoma | Hepatocellular adenoma (HA) is a rare benign tumor of the liver |
1 | list | Hereditary angioedema | Hereditary angioedema (HAE) is a genetic disease characterized by the occurrence of transitory and recurrent subcutaneous and/or submucosal edemas resulting in swelling and/or abdominal pain |
1 | list | Geniospasm | Hereditary geniospasm is a movement disorder characterized by episodes of involuntary tremor of the chin and lower lip |
1 | list | Hereditary leiomyomatosis and renal cell cancer syndrome | Hereditary leiomyomatosis and renal cell cancer (HLRCC) is a hereditary cancer syndrome characterized by a predisposition to cutaneous and uterine leiomyomas and, in some families, to renal cell cancer |
1 | list | Herpes labialis | Herpes simplex virus that primarily affects the lip |
1 | list | Coxa vara | Hip deformity in which the femoral neck leans forward resulting in a decrease in the angle between femoral neck and its shaft. It may be congenital often syndromic, acquired, or developmental. |
1 | list | Emphysematous cystitis | Hip fracture right |
1 | list | Young–Madders syndrome | Holoprosencephaly-postaxial polydactyly syndrome associates, in chromosomally normal neonates, holoprosencephaly, severe facial dysmorphism, postaxial polydactyly and other congenital abnormalities, suggestive of trisomy 13 (see this term) |
1 | list | Subphrenic abscess | Hoover's sign |
1 | list | Central nervous system viral disease | Human |
1 | list | Carpal tunnel syndrome | Human Syndrome |
1 | list | Acromegaly | Human disease / micro cephaly opposite |
1 | list | Mumps | Human disease caused by paramyxovirus |
1 | list | Ileus | Human disease characterized by impairment of intestinal peristalsis; in modern language usually excludes mechanical bowel obstruction |
1 | list | Horner's syndrome | Human disease characterized by miosis (a constricted pupil), partial ptosis (a weak, droopy eyelid), apparent anhydrosis (decreased sweating), with apparent enophthalmos (inset eyeball) |
1 | list | Kawasaki disease | Human disease in which blood vessels throughout the body become inflamed |
1 | list | Double outlet right ventricle | Human disease, Congenital Heart Disease |
1 | list | Diabetes insipidus | Human disease, a condition characterized by large amounts of dilute urine and increased thirst |
1 | list | Werner syndrome | Human disease. Common in 1 in 2 children. Death is inevitable. |
1 | list | Hydrops fetalis | Human disease. The abnormal accumulation of fluid in two or more fetal compartments, including ascites, pleural effusion, pericardial effusion, and skin edema. |
1 | list | Hypermobility (joints) | Human disease: joints that stretch farther than normal |
1 | list | Adhesive capsulitis of shoulder | Human disease: painful and disabling disorder of unclear cause in which the shoulder capsule |
1 | list | Lemierre's syndrome | Human disease: infectious thrombophlebitis of the internal jugular vein |
1 | list | Yaws | Human disease: tropical infection of the skin, bones and joints caused by the spirochete bacterium Treponema pallidum pertenue |
1 | list | Toxic multinodular goitre | Human diseasexdr dildar |
1 | list | Haemophilia | Human genetic disease that impairs the body's ability to make blood clots, a process needed to stop bleeding |
1 | list | Vitreomacular adhesion | Human medical condition |
1 | list | Monckeberg's arteriosclerosis | Human pathology |
1 | list | Dysplastic nevus syndrome | Human skin disease |
1 | list | Chickenpox | Human viral disease |
1 | list | Pinworm infection | Human worm infection |
1 | list | Viral disease | Human, animal or plant disease resulting from a viral infection |
1 | list | Huntington's disease | Huntington disease (HD) is a rare neurodegenerative disorder of the central nervous system characterized by unwanted choreatic movements, behavioral and psychiatric disturbances and dementia |
1 | list | Cuckold | Husband of an adulterous wife, or males unwittingly investing effort in others' offspring |
1 | list | Chalazion | Huuggblepharitis that is characterized as a cyst in the eyelid that is caused by inflammation of a blocked meibomian gland, usually on the upper eyelid |
1 | list | Ichthyosis follicularis with alopecia and photophobia syndrome | Ichthyosis follicularis - alopecia - photophobia (IFAP) is a rare genetic disorder characterized by the triad of ichthyosis follicularis, alopecia, and photophobia from birth |
1 | list | Idiopathic hypersomnia | Idiopathic hypersomnia is a sleep disorder classified in two forms: idiopathic hypersomnia with long sleep time and idiopathic hypersomnia without long sleep time |
1 | list | Klismaphilia | In human sexuality, a paraphilia involving enjoyment of, and sexual arousal from, enemas. |
1 | list | Agalmatophilia | Inanimate Object Love |
1 | list | 1971 Iraq poison grain disaster | Incident of mass poisoning in Iraq in 1971 |
1 | list | Mydriasis | Increase of the pupil's diameter and dilation |
1 | list | Opportunistic infection | Infection that takes advantage of one or more factors |
1 | list | Gram-negative bacterial infection | Infections caused by bacteria that show up as pink (negative) when treated by the gram-staining method |
1 | list | Intestinal parasite infection | Infections of the INTESTINES with PARASITES, commonly involving PARASITIC WORMS. Infections with roundworms (NEMATODE INFECTIONS) and tapeworms (CESTODE INFECTIONS) are also known as HELMINTHIASIS. |
1 | list | Pseudomonas infection | Infections with bacteria of the genus pseudomonas |
1 | list | Southern tick-associated rash illness | Infectious disease transmitted by ticks |
1 | list | Enthesitis | Inflammation at the site of insertion of ligaments, tendons, and other fibrous structures into bone |
1 | list | Neuritis | Inflammation of a nerve or the general inflammation of the peripheral nervous system |
1 | list | Hemorrhagic cystitis | Inflammation of the bladder resulting in bloody urine |
1 | list | Cryptogenic organizing pneumonia | Inflammation of the bronchioles (bronchiolitis) and surrounding tissue in the lungs |
1 | list | Proctocolitis | Inflammation of the rectum and colon |
1 | list | Chronic gastritis | Inflammation of the stomach that is chronic in nature |
1 | list | Panniculitis | Inflammation of the subcutaneous adipose tissue |
1 | list | Tonsillitis | Inflammation of the tonsils |
1 | list | Trigonitis | Inflammation of the trigone of the urinary bladder |
1 | list | Urethritis | Inflammation of the urethra |
1 | list | Fasciitis | Inflammation process in fascia |
1 | list | Psoas muscle abscess | Infundibulum |
1 | list | Dahan syndrome | Injury to the pituitary gland, resulting from spasm of the arteries. Where the pituitary gland produces less or no hormones due to the injury |
1 | list | Vulvar intraepithelial neoplasia | Intraepithelial neoplasia of the vulvar squamous epithelium. There is no evidence of invasion. This category includes vulvar high grade squamous intraepithelial lesion and vulvar intraepithelial neoplasia, differentiated type. |
1 | list | Iron deficiency (plant disorder) | Iron deficiency (plant disorder) |
1 | list | Auricular hypertrichosis | Is a genetic condition expressed as long and strong hairs growing from the helix of the pinna. |
1 | list | Neuromyotonia | Isaac's syndrome is an immune-mediated peripheral motor neuron disorder characterized by continuous muscle fiber activity at rest resulting in muscle stiffness, cramps, myokymia, and pseudomyotonia |
1 | list | Acropachy | Isolated congenital digital clubbing is a rare genodermatosis disorder characterized by enlargement of the terminal segments of fingers and toes with thickened nails without any other abnormality |
1 | list | Rocker bottom foot | Isolated congenital vertical talus (CVT) is a rare pedal deformity recognizable at birth by a dislocation of the talonavicular joint, resulting in a characteristic radiographic near-vertical orientation of the talus |
1 | list | Lazarus and Joannes Baptista Colloredo | Italian conjoined twins |
1 | list | Jacobsen syndrome | Jacobsen syndrome is a multiple congenital anomaly/mental retardation (MCA/MR) contiguous gene syndrome caused by partial deletion of the long arm of chromosome 11 |
1 | list | Jalili syndrome | Jalili syndrome is characterized by the association of amelogenesis imperfecta (AI; see this term) and cone-rod retinal dystrophy (CORD; see this term) |
1 | list | Taijin kyofusho | Japanese culture-bound syndrome |
1 | list | Itai-itai disease | Japanese epidemic of cadmium poisoning |
1 | list | Niigata Minamata disease | Japanese outbreak of mercury poisoning |
1 | list | Jessner lymphocytic infiltrate of the skin | Jessner lymphocytic infiltration of the skin (JLIS) is a chronic benign cutaneous disease characterized by asymptomatic non-scaly erythematous papules or plaques on the face and neck |
1 | list | Johnson–McMillin syndrome | Johnson neuroectodermal syndrome is characterised by alopecia, anosmia or hyposmia, conductive deafness with malformed ears and microtia and/or atresia of the external auditory canal, and hypogonadotropic hypogonadism |
1 | list | Joubert syndrome | Joubert syndrome (JS) is characterized by congenital malformation of the brainstem and agenesis or hypoplasia of the cerebellar vermis leading to an abnormal respiratory pattern, nystagmus, hypotonia, ataxia, and delay in achieving motor milestones |
1 | list | African cutaneous Kaposi sarcoma | Kaposi's sarcoma that is located in black Africans |
1 | list | Kapur–Toriello syndrome | Kapur-Toriello syndrome is an extremely rare syndrome characterized by facial dysmorphism, severe intellectual deficiency, cardiac and intestinal anomalies, and growth retardation |
1 | list | Spinal and bulbar muscular atrophy | Kennedy's disease, also known as bulbospinal muscular atrophy (BSMA), is a rare X-linked recessive motor neuron disease characterized by proximal and bulbar muscle wasting |
1 | list | Keutel syndrome | Keutel syndrome is characterised by diffuse cartilage calcification, brachytelephalangism, peripheral pulmonary artery stenoses and facial dysmorphism |
1 | list | Kienböck's disease | Kienbock disease is a rare bone disorder of unknown etiology characterized clinically by osteonecrosis of the carpal lunate, eventually leading to collapse of the lunate bone impacting wrist function |
1 | list | Knobloch syndrome | Knobloch syndrome (KS) is defined by vitreoretinal and macular degeneration, and occipital encephalocele |
1 | list | Leukonychia | Known as a cresent moon on your nail |
1 | list | Kohlschütter-Tönz syndrome | KohlschC<tter-TC6nz syndrome (KTS) is a genetically heterogeneous autosomal recessive syndrome characterized by the triad of amelogenesis imperfect, infantile onset epilepsy, intellectual disability with or without regression and dementia |
1 | list | Krabbe disease | Krabbe disease is a lysosomal disorder that affects the white matter of the central and peripheral nervous systems. It includes infantile, late-infantile/juvenile and adult forms. |
1 | list | Kufor–Rakeb syndrome | Kufor-Rakeb syndrome (KRS) is a rare genetic neurodegenerative disorder characterized by juvenile Parkinsonism, pyramidal degeneration (dystonia), supranuclear palsy, and cognitive impairment |
1 | list | Disinhibition | Lack of social and/or behavioral restraint |
1 | list | Lafora disease | Lafora disease (LD) is a rare, inherited, severe, progressive myoclonic epilepsy characterized by myoclonus and/or generalized seizures, visual hallucinations (partial occipital seizures), and progressive neurological decline |
1 | list | Langer mesomelic dysplasia | Langer mesomelic dysplasia (LMD) is characterized by severe disproportionate short stature with mesomelic and rhizomelic shortening of the upper and lower limbs |
1 | list | Lathosterolosis | Lathosterolosis is an extremely rare inborn error of sterol biosynthesis characterized by facial dysmorphism, congenital anomalies (including limb and kidney anomalies), failure to thrive, developmental delay and liver disease |
1 | list | Legius syndrome | Legius syndrome, also known as NF1-like syndrome, is a rare, genetic skin pigmentation disorder characterized by multiple cafC)-au-lait macules with or without axillary or inguinal freckling |
1 | list | Lelis syndrome | Lelis syndrome is characterised by the association of ectodermal dysplasia (hypotrichosis and hypohidrosis) with acanthosis nigricans |
1 | list | Lenz–Majewski syndrome | Lenz-Majewski hyperostotic dwarfism is an extremely rare syndrome associating dwarfism, characteristic facial appearance, cutis laxa and progressive bone sclerosis |
1 | list | Lethal acantholytic epidermolysis bullosa | Lethal acantholytic epidermolysis bullosa is a suprabasal subtype of epidermolysis bullosa simplex (EBS, see this term) characterized by generalized oozing erosions, usually in the absence of blisters |
1 | list | Arts syndrome | Lethal ataxia with deafness and optic atrophy (also known as Arts syndrome) is characterized by intellectual deficit, early-onset hypotonia, ataxia, delayed motor development, hearing impairment and loss of vision due to optic atrophy |
1 | list | Raine syndrome | Lethal osteosclerotic bone dysplasia is defined by generalized osteosclerosis with periosteal bone formation, characteristic facial dysmorphism, brain abnormalities including intracerebral calcifications, and neonatal lethal course |
1 | list | Leukotriene C4 synthase deficiency | Leukotriene C4 synthase deficiency is an extremely rare fatal neurometabolic developmental disorder characterized clinically by muscular hypotonia, psychomotor retardation, failure to thrive, and microcephaly |
1 | list | Lichen planopilaris | Lichen planopilaris (LPP) is a rare cutaneous variant of lichen planus (see this term) which affects hair follicles. It may occur on its own or in association with more common forms of lichen planus, usually classical type and/or oral lichen planus. |
1 | list | Flail chest | Life-threatening medical condition that occurs when a segment of the rib cage breaks due to trauma and becomes detached from the rest of the chest wall |
1 | list | Milium (dermatology) | Light-coloured spots under the skin |
1 | list | Limb body wall complex | Limb body wall complex (LBWC) is characterized by severe multiple congenital anomalies in the fetus with exencephaly/encephalocele, thoraco- and/or abdominoschisis (anterior body wall defects) and limb defects, with or without facial clefts |
1 | list | Linear lichen planus | Linear lichen planus (LLP), also referred to as Blaschkoid LP, is a rare type of lichen planus characterized by a linear distribution of lichenoid lesions along the lines of Blaschko, which are embryonic pathways of skin development |
1 | list | Localized lipodystrophy | Localised lipodystrophies are characterised by loss of subcutaneous tissue from small regions of the body |
1 | list | Unicentric Castleman disease | Localized Castleman disease (LCD) is the most common form of Castleman disease (CD; see this term) and it is usually asymptomatic or it may present with enlarged lymph nodes. LCD may be cured by surgical resection. |
1 | list | Hypertension | Long term medical condition |
1 | list | Downblouse | Looking at breasts without permission |
1 | list | Lowry–MacLean syndrome | Lowry-MacLean syndrome is a very rare syndrome characterized by microcephaly, craniosynostosis, glaucoma, growth failure and visceral malformations |
1 | list | Multiple complex developmental disorder | MCDD |
1 | list | Hurler–Scheie syndrome | MPS - I H/S: cutaneous condition, also characterized by mild mental retardation and corneal clouding |
1 | list | Madelung's deformity | Madelung disease, or deformity (MD) is a predominantly bilateral wrist anomaly characterized by shortened and bowed radii and long ulnae leading to dorsal dislocation of the distal ulna and limited mobility of the wrist and elbow |
1 | list | Madras motor neuron disease | Madras motor neuron disease (MMND) is characterized by weakness and atrophy of limbs, multiple lower cranial nerve palsies and sensorineural hearing loss |
1 | list | Majeed syndrome | Majeed syndrome is a rare genetic multisystemic disorder characterized by the triad of chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anemia, and variable transient inflammatory dermatosis |
1 | list | 1592–93 London plague | Major plague outbreak in England |
1 | list | Malakoplakia | Malakoplakia is a chronic multisystem granulomatous inflammatory disease characterized by the presence of single or multiple soft plaques on various organs of the body |
1 | list | Y chromosome microdeletion | Male sterility due to chromosome Y deletion is characterized by a severe deficiency of spermatogenesis. Chromosome Y deletions are a frequent genetic cause of male infertility. |
1 | list | Malonyl-CoA decarboxylase deficiency | Malonic aciduria is a metabolic disorder caused by deficiency of malonyl-CoA decarboxylase (MCD) |
1 | list | Coccidioidomycosis | Mammalian disease caused by Coccidioides fungi |
1 | list | Fleischer's syndrome | Mammo-renal syndrome |
1 | list | Marinesco–Sjögren syndrome | Marinesco-Sjogren syndrome (MSS) belongs to the group of autosomal recessive cerebellar ataxias. Cardinal features of MSS are cerebellar ataxia, congenital cataract, and delayed psychomotor development. |
1 | list | Diabetes and deafness | Maternally inherited diabetes and deafness (MIDD) is a mitochondrial disorder characterized by maternally transmitted diabetes and sensorineural deafness |
1 | list | McKusick–Kaufman syndrome | McKusick-Kaufman syndrome is a very rare, genetic developmental disorder presenting in the neonatal period characterized by genitourinary malformations, polydactyly, and more rarely, congenital heart disease or gastrointestinal malformations |
1 | list | Neonatal withdrawal | Medical condition in newborn babies caused by drugs taken by the mother before birth |
1 | list | Biliary colic | Medical condition in which gallstones cause acute pain |
1 | list | Dancing mania | Medieval social phenomena |
1 | list | Survivor guilt | Mental condition |
1 | list | Metachondromatosis | Metachondromatosis (MC) is a rare disorder characterized by the presence of both multiple enchondromas and osteochondroma-like lesions |
1 | list | Cryoglobulinemic vasculitis | Mixed cryoglobulinemia (MC) is a rare multisystem disease characterized by the presence of circulating cryoprecipitable immune complexes in the serum, manifested clinically by a classical triad of purpura, weakness and arthralgia |
1 | list | Mooncalf | Monstrous birth |
1 | list | Malaria | Mosquito-borne infectious disease |
1 | list | Spastic ataxia-corneal dystrophy syndrome | Mousa-AlDin-AlNassar syndrome is characterised by the presence of spastic ataxia in association with bilateral congenital cataract, corneal dystrophy, and nonaxial myopia |
1 | list | Multifocal motor neuropathy | Multifocal motor neuropathy (MMN) is a rare acquired immune-mediatedneuropathy characterized clinically by a purely motor deficit with conduction block and asymmetric multifocal weakness, fasciculations, and cramping |
1 | list | Multiple system atrophy | Multiple system atrophy (MSA) is a neurodegenerative disorder characterized by autonomic failure (cardiovascular and/or urinary), parkinsonism, cerebellar impairment and corticospinal signs with a median survival of 6-9 years |
1 | list | Phakomatosis | Multisystem disorders that involve the ectodermal structures like central nervous system, skin and eyes. |
1 | list | Photic sneeze reflex | Muscle contracture that allows our eyes to adjust to brighter conditions |
1 | list | Kocher–Debre–Semelaigne syndrome | Muscular pseudohypertropy - hypothyroidism, also known as Kocher-Debre-Semelaigne syndrome is a rare disorder characterized by pseudohypertrophy of muscles due to longstanding hypothyroidism (see this term) |
1 | list | N-Acetylglutamate synthase deficiency | N-acetylglutamate synthase (NAGS) deficiency is a urea cycle disorder leading to hyperammonaemia |
1 | list | Naegeli–Franceschetti–Jadassohn syndrome | Naegeli-Franceschetti-Jadassohn (NFJ) syndrome is a rare ectodermal dysplasia that affects the skin, sweat glands, nails, and teeth |
1 | list | Naxos syndrome | Naxos disease is a recessively inherited condition with arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) and a cutaneous phenotype, characterised by peculiar woolly hair and palmoplantar keratoderma |
1 | list | Neuroacanthocytosis | Neuroacanthocytosis (NA) syndromes are a group of genetic diseases characterized by the association of red blood cell acanthocytosis (deformed erythrocytes with spike-like protrusions) and progressive degeneration of the basal ganglia |
1 | list | Neuroendocrine hyperplasia | Neuroendocrine cell hyperplasia of infancy (NCHI) is a non-lethal pediatric form of interstitial lung disease (ILD, see this term) characterized by tachypnea without respiratory failure |
1 | list | Neuroferritinopathy | Neuroferritinopathy is a late-onset type of neurodegeneration with brain iron accumulation (NBIA; see this term) characterized by progressive chorea or dystonia and subtle cognitive deficits |
1 | list | Neuropathy, ataxia, and retinitis pigmentosa | Neuropathy, Ataxia, and Retinitis Pigmentosa (NARP) syndrome is a clinically heterogeneous progressive condition characterized by a combination of proximal neurogenic muscle weakness, sensory-motor neuropathy, ataxia, and pigmentary retinopathy |
1 | list | Autistic enterocolitis | Nonexistent medical condition invented in fraudulent study by Andrew Wakefield |
1 | list | Hospital-acquired infection | Nosocomial Infections |
1 | list | Congenital insensitivity to pain | Not feeling pain |
1 | list | Genu varum | O-knees |
1 | list | OSLAM syndrome | OSLAM syndrome is characterised by the association of osteosarcoma, limb anomalies (clinodactyly with brachymesophalangy, bilateral radioulnar synostosis and absence of one digital ray of the foot) and red cell macrocytosis without anaemia |
1 | list | Obstructive shock | Obstructive shock is a form of shock associated with physical obstruction of the great vessels or the heart itself. |
1 | list | Occipital horn syndrome | Occipital horn syndrome (OHS) is a mild form of Menkes disease (MD, see this term), a syndrome characterized by progressive neurodegeneration and connective tissue disorders due to a copper transport defect |
1 | list | Oculocerebrocutaneous syndrome | Oculocerebrocutaneous syndrome (OCCS) is a rare congenital disorder associated with an intellectual disability and is typically characterized by the triad of eye, central nervous system and skin malformations |
1 | list | Oculopharyngeal muscular dystrophy | Oculopharyngeal muscular dystrophy (OPMD) is an adult-onset progressive myopathy characterized by progressive eyelid ptosis, dysphagia, dysarthria and proximal limb weakness |
1 | list | Opsismodysplasia | Opsismodysplasia is a skeletal dysplasia characterized by congenital dwarfism and facial dysmorphism |
1 | list | Oral florid papillomatosis | Oral mucosal pathology |
1 | list | PEHO syndrome | PEHO (Progressive encephalopathy with Edema, Hypsarrhythmia and Optic atrophy) syndrome is a rare neurodegenerative disorder belonging to the group of infantile progressive encephalopathies |
1 | list | PELVIS syndrome | PELVIS is an acronym defining the association of Perineal hemangioma, External genitalia malformations, Lipomyelomeningocele, Vesicorenal abnormalities, Imperforate anus, and Skin tag. Eleven cases have been reported. |
1 | list | Periodic fever, aphthous stomatitis, pharyngitis and adenitis | PFAPA (Periodic fever - aphthous stomatitis- pharyngitis - adenopathy) syndrome is an auto inflammatory syndrome characterized by recurrent febrile episodes associated with aphthous stomatitis, pharyngitis and cervical adenitis |
1 | list | Vaginismus | Painful vaginal penetration without a physical cause. |
1 | list | Papular mucinosis of infancy | Papular mucinosis of infancy is a rare pediatric non progressive form of localized lichen myxedematosus (see this term) characterized by the development of firm opalescent mucinous papules on the upper arms and the trunk |
1 | list | Sowda | Parasitic infestation |
1 | list | Parastremmatic dwarfism | Parastremmatic dwarfism is a very rare chondrodysplasia characterized by severe dwarfism, kyphoscoliosis, stiffness of large joints and distortion of lower limbs |
1 | list | Paris-Trousseau syndrome | Paris-Trousseau thrombocytopenia (TCPT) is a contiguous gene syndrome characterized by mild bleeding tendency, variable thrombocytopenia (THC), dysmorphic facies, abnormal giant alpha-granules in platelets and dysmegakaryopoiesis |
1 | list | Paroxysmal exercise-induced dystonia | Paroxysmal exertion-induced dyskinesia (PED) is a form of paroxysmal dyskinesia (see this term), characterized by painless attacks of dystonia of the extremities triggered by prolonged physical activities |
1 | list | Paroxysmal extreme pain disorder | Paroxysmal extreme pain disorder is a rare disorder of abnormal pain sensation |
1 | list | Bee sting | Part of a bee's anatomy. |
1 | list | Sluggish cognitive tempo | Particular type of attention disorder |
1 | list | Pneumoretroperitoneum | Pathological or accidental introduction of air into the retroperitoneal space. |
1 | list | Bacterial wilt of turfgrass | Pathovar of bacteria |
1 | list | Paraneoplastic pemphigus | Pemphigus is a group of chronic autoimmune skin diseases characterised by blisters formation on the outer layer of the skin and the mucous membranes. Three clinical forms have been characterised, of which paraneoplastic pemphigus is extremely rare. |
1 | list | Tarlov cyst | Perineural (or Tarlov) cysts are cerebrospinal fluid-filled nerve root cysts most commonly found at the sacral level of the spine, although they can be found in any section of the spine, which can cause progressively painful radiculopathy |
1 | list | Antisocial personality disorder | Personality disorder that involves a pervasive pattern of disregard for other people |
1 | list | Postpartum psychosis | Peurperal psychosis |
1 | list | Phakomatosis pigmentokeratotica | Phakomatosis pigmentokeratotica (PPK) is a very rare epidermal nevus disorder characterized by the association of speckled lentiginous nevi with epidermal sebaceous nevi, and extracutaneous anomalies |
1 | list | Pseudophobia | Phobia |
1 | list | Polydactyly | Physical anomaly |
1 | list | Accessory nail of the fifth toe | Physical human trait |
1 | list | Potassium deficiency (plants) | Plant disorder |
1 | list | Pneumonitis | Pneumonitis is a general term that refers to inflammation of lung tissue. |
1 | list | Anti-MAG peripheral neuropathy | Polyneuropathy associated with IgM monoclonal gammapathy (MG) with anti-MAG (myelin-associated-glycoprotein) activity is a demyelinating polyneuropathy characterized clinically by sensory ataxia, tremor, paresthesia, and impaired gait |
1 | list | Complications of traumatic brain injury | Possible consequences of a brain injury |
1 | list | Anetoderma | Primary anetoderma is a rare skin disease characterized by loss of elastin tissue resulting in localized areas of flaccid skin in the absence of a secondary cause |
1 | list | Primary effusion lymphoma | Primary effusion lymphoma (PEL) is a large B-cell lymphoma located in the body cavities, characterized by pleural, peritoneal, and pericardial fluid lymphomatous effusions and that is always associated with human herpes virus-8 (HHV-8) |
1 | list | Occupational lung disease | Professional Lung Disease |
1 | list | Sarcopenia | Progressive decline in muscle mass due to aging which results in decreased functional capacity of muscles |
1 | list | Copenhagen disease | Progressive non-infectious anterior vertebral fusion (PAVF) is an early childhood spinal disorder characterized by the gradual onset of thoracic and/or lumbar spine ankylosis often in conjunction with kyphosis with distinctive radiological features |
1 | list | Progressive supranuclear palsy | Progressive supranuclear palsy (PSP) is a rare late-onset neurodegenerative disease characterized by supranuclear gaze palsy, postural instability, progressive rigidity, and mild dementia |
1 | list | Contracture | Prolonged shortening of the muscle or other soft tissue around a joint, preventing movement of the joint |
1 | list | Proteus-like syndrome | Proteus-like syndrome describes patients who do not meet the diagnostic criteria for Proteus syndrome (see this term) but who share a multitude of characteristic clinical features of the disease |
1 | list | Prognathism | Protrusion of the upper or lower human jaw |
1 | list | Childbirth-related posttraumatic stress disorder | Psychiatric disorder associated with childbirth |
1 | list | Pudendal nerve entrapment | Pudendal neuralgia (PN) is a chronic neuropathic pain, aggravated by sitting and for which no organic cause can be found by imaging studies. It is often associated with pelvic dysfunction. |
1 | list | Pulmonary toxicity | Pulmonary toxicity is the medical name for side effects on the lungs. |
1 | list | Pure autonomic failure | Pure autonomic failure (PAF) is a neurodegenerative disease that affects the sympathetic branch of the autonomous nervous system and that manifests with orthostatic hypotension |
1 | list | Pyoderma | Pyoderma is a skin infectious disease where the infection is pyogenic causing the formation of pus |
1 | list | PAPA syndrome | Pyogenic arthritis-pyoderma gangrenosum-acne syndrome is a rare pleiotropic autoinflammatory disorder of childhood, primarily affecting the joints and skin |
1 | list | Quebec platelet disorder | Quebec platelet syndrome (QPS) is a platelet granule disorder characterized by moderate to severe bleeding after trauma, surgery or obstetric interventions, frequent ecchymoses, mucocutaneous bleeding and muscle and joint bleeds |
1 | list | Spectrum disorder | RLS IS A SPECTRUM DISORDER |
1 | list | Radial dysplasia | Radial hemimelia is a congenital longitudinal deficiency of the radius bone of the forearm characterized by partial or total absence of the radius |
1 | list | Radiation proctitis | Radiation proctitis is a rare rectal disease directly induced by pelvic radiotherapy and characterized by rectal bleeding, change in bowel habits, tenesmus and sepsis |
1 | list | Morquio syndrome | Rare Disease |
1 | list | T-cell lymphoma | Rare T-cell lymphoma |
1 | list | Schindler disease | Rare congenital metabolic disorder in humans. |
1 | list | Germ cell tumor | Rare germ cell tumor |
1 | list | Retroperitoneal fibrosis | Related to igG4-related disease |
1 | list | Perinatal asphyxia | Respiratory failure in the newborn. (Dorland, 27th ed) |
1 | list | Retinoblastoma | Retinal cell cancer |
1 | list | Reynolds syndrome | Reynolds syndrome (RS) is an autoimmune disorder characterized by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc) (see these terms) |
1 | list | Rhinitis medicamentosa | Rhinitis induced by descongestants |
1 | list | Rhombencephalosynapsis | Rhombencephalosynapsis (RS) is a rare malformation of the cerebellum characterised by the association of agenesis (total or partial) of the vermis and fusion of the cerebellar hemispheres |
1 | list | Anastasia and Tatiana Dogaru | Romanian conjoined twins |
1 | list | Rombo syndrome | Rombo syndrome is characterized by vermiculate atrophoderma, milia, hypotrichosis, trichoepitheliomas, peripheral vasodilation with cyanosis and basal cell carcinomas |
1 | list | Rotator cuff tear | Rotator cuff tear |
1 | list | Penile fracture | Rupture of one or both of the tunica albuginea, the fibrous coverings that envelop the penis's corpora cavernosa |
1 | list | Masha and Dasha Krivoshlyapova | Russian conjoined twins |
1 | list | Saccharopinuria | Saccharopinuria is a disorder of lysine metabolism associated with hyperlysinaemia and lysinuria |
1 | list | Sandhoff disease | Sandhoff disease is a lysosomal storage disorder from the GM2 gangliosidosis family and is characterised by central nervous system degeneration |
1 | list | Sarcosinemia | Sarcosinemia is a metabolic disorder characterized by an increased concentration of sarcosine in plasma and urine due to sarcosine dehydrogenase deficiency |
1 | list | Schöpf–Schulz–Passarge syndrome | SchC6pf-Schulz-Passarge syndrome (SSPS) is a rare autosomal recessive ectodermal dysplasia characterized by multiple eyelid apocrine hidrocystomas, palmoplantar keratoderma, hypotrichosis, hypodontia and nail dystrophy |
1 | list | Schinzel–Giedion syndrome | Schinzel-Giedion syndrome (SGS) is an ectodermal dysplasia syndrome chiefly characterized by a distinctive facial dysmorphism, hydronephrosis, severe developmental delay, typical skeletal malformations, and genital and cardiac anomalies |
1 | list | EAST syndrome | SeSAME syndrome is characterized by seizures, sensorineural deafness, ataxia, intellectual deficit, and electrolyte imbalance (hypokalemia, metabolic alkalosis, and hypomagnesemia) |
1 | list | Euthyroid sick syndrome | Secondary allostasis of thyroid function in fetal life, starving and in critical illness |
1 | list | Serotonin syndrome | Serotoninergic syndrome is characterised by an excess of serotonin in the central nervous system, associated with the use of various agents, including selective serotonin reuptake inhibitors (SSRIs) |
1 | list | Toxic epidermal necrolysis | Severe skin reaction |
1 | list | Coprophilia | Sexual paraphilia involving feces |
1 | list | Shellfish poisoning | Shellfish poisoning. |
1 | list | Silent sinus syndrome | Silent sinus syndrome is characterised by adult-onset progressive enophthalmos due to collapse of some or all of the maxillary sinus walls |
1 | list | Herpesviral meningitis | Simplexvirus infectious disease that results in inflammation located in meninges, has material basis in Human herpesvirus 2 and has symptom headache, has symptom fever, and has symptom meningism |
1 | list | Sinding-Larsen and Johansson syndrome | Sinding-Larsen-Johansson disease is a type of osteochondrosis affecting the attachment of the patellar tendon to the patella and characterised by tenderness and localized swelling of the patella |
1 | list | Sinus bradycardia | Sinus bradycardia is a sinus rhythm with a rate that is lower than normal |
1 | list | Upper motor neuron syndrome | Skeletal muscle syndrome |
1 | list | Hypertrophic scar | Skin condition |
1 | list | Ischiopatellar dysplasia | Small patella syndrome (SPS) is a very rare benign bone dysplasia affecting skeletal structures of the lower limb and the pelvis |
1 | list | Hyponatremia | Sodium/Electrolytic Deficit Symptoms |
1 | list | Sphincter of Oddi dysfunction | Sphincter of Oddi |
1 | list | Spinal shock | Spinal shock was defined as a loss of sensation accompanied by motor paralysis with initial loss but gradual recovery of reflexes, following a spinal cord injury |
1 | list | Spinocerebellar ataxia type 1 | Spinocerebellar ataxia type 1 (SCA1) is a subtype of type I autosomal dominant cerebellar ataxia (ADCA type I; see this term) characterized by dysarthria, writing difficulties, limb ataxia, and commonly nystagmus and saccadic abnormalities |
1 | list | Teunissen–Cremers syndrome | Stapes ankylosis with broad thumbs and toes is a very rare genetic bone disorder characterized by ankylosis of stapes, broad thumbs and halluces, conductive hearing loss and hyperopia |
1 | list | Anesthesia awareness | State of inadequate unconsciousness during general anesthesia |
1 | list | Stickler syndrome | Stickler syndrome is an inherited vitreoretinopathy characterized by the association of ocular signs with more or less complete forms of Pierre-Robin sequence (see this term), bone disorders, and sensorineural deafness (10% of cases) |
1 | list | PANDAS | Streptococcus triggered misdirected immune response resulting in inflammation on a child’s brain leading to OCD, anxiety, tics, personality Pandas also have a tree obsession and like eating oranges |
1 | list | Beet vascular necrosis | Subspecies of bacteria |
1 | list | Precursor B-cell lymphoblastic leukemia | Subtype of acute lymphoblastic leukemia (ALL) |
1 | list | Succinyl-CoA:3-oxoacid CoA transferase deficiency | Succinyl-CoA:3-ketoacid CoA transferase deficiency (SCOTD) is a defect in ketone body utilization characterized by severe, potentially fatal intermittent episodes of ketoacidosis |
1 | list | Takotsubo cardiomyopathy | Sudden temporary weakening of the heart muscle |
1 | list | Fusarium wilt | Suomeksi |
1 | list | Ichthyosis bullosa of Siemens | Superficial epidermolytic ichthyosis (SEI) is a rare keratinopathic ichthyosis (KI; see this term) characterized by the presence of superficial blisters and erosions at birth |
1 | list | Subcutaneous emphysema | Surgical Emphysema |
1 | list | Excessive daytime sleepiness | Symptom characterized by persistent sleepiness during daytime |
1 | list | Blurred vision | Symptom, lack of sharpness of vision resulting in the inability to see fine detail. http://purl.obolibrary.org/obo/HP_0000622 [HPO: probinson]. |
1 | list | DiGeorge syndrome | Synonym for 22q11.2 deletion syndrome. T cell deficiency disease that is the result of a large deletion of chromosome 22 which includes the DGS gene needed for development of the thymus and related glands with subsequent lack of T-cell production |
1 | list | Systemic-onset juvenile idiopathic arthritis | Systemic-onset juvenile idiopathic arthritis is marked by the severity of the extra-articular manifestations (fever, cutaneous eruptions) and by an equal sex ratio |
1 | list | TEMPI syndrome | TEMPI syndrome is a rare multi-systemic disease characterized by the presence of Telangiectasias, Erythrocytosis with elevated erythropoietin levels, Monoclonal gammopathy, Perinephric-fluid collections, and Intrapulmonary shunting |
1 | list | Terminal osseous dysplasia with pigmentary defects | Terminal osseous dysplasia-pigmentary defects syndrome is characterised by malformation of the hands and feet, pigmentary skin lesions on the face and scalp and digital fibromatosis |
1 | list | Chang and Eng Bunker | Thai-American conjoined twin brothers |
1 | list | XXXY syndrome | The 48,XXXY syndrome represents a chromosomal anomaly of the aneuploidic type characterized by the presence of two extra X chromosomes in males |
1 | list | XXYY syndrome | The 48,XXYY syndrome represents a chromosomal anomaly of the aneuploidic type characterized by the presence of an extra X and Y chromosome in males |
1 | list | 49,XXXXY | The 49,XXXXY syndrome represents a chromosomal anomaly of the aneuploidic type characterized by the presence of three extra X chromosomes in males |
1 | list | Nablus mask-like facial syndrome | The 8q22.1 microdeletion syndrome or Nablus mask-like facial syndrome is a rare microdeletion syndrome associated with a distinct facial appearance. |
1 | list | Oculomotor apraxia | The absence or defect of controlled, voluntary, and purposeful eye movement |
1 | list | Cat bite | The bite of the domestic cat |
1 | list | Mucometrocolpos | The build of mucous behind an imperforate hymen |
1 | list | Inverted nipple | The case where the nipple is turned inside the breast |
1 | list | Amaurotic nystagmus | The nystagmus associated with blindness or the central vision defects. |
1 | list | Ronnie and Donnie Galyon | The oldest living conjoined twins |
1 | list | Somniloquy | The phenomenon of talking while asleep. |
1 | list | Parasitemia | The presence of parasites (especially malarial parasites) in the blood. (Dorland, 27th ed) |
1 | list | Disfigurement | The state of having one's appearance harmed by a medical or physical procedure. |
1 | list | Thiamine responsive megaloblastic anemia syndrome | Thiamine-responsive megaloblastic anemia (TRMA) is characterized by a triad of megaloblastic anemia, non-type I diabetes mellitus, and sensorineural deafness |
1 | list | Pain management in children | This is a description of the medical condition of pain in children, its assessment, treatment and prevention |
1 | list | Malouf syndrome | This syndrome is characterized by the association of dilated cardiomyopathy and hypergonadotropic hypogonadism (DCM-HH) |
1 | list | De Quervain's thyroiditis | Thyroid disease |
1 | list | Graves' ophthalmopathy | Thyroid eye disease (TED), often associated with Graves' disease. |
1 | list | Hürthle cell | Thyroid follicles lined by deeply eosinophilic Hürthle cells are seen in Hashimoto disease |
1 | list | Paris syndrome | Tourist experience of being overwhelmed by finally visiting Paris |
1 | list | Transient bullous dermolysis of the newborn | Transient bullous dermolysis of the newborn is a rare subtype of dystrophic epidermolysis bullosa (DEB, see this term) characterized by generalized blistering at birth that usually regresses within the first 6 to 24 months of life |
1 | list | Postperfusion syndrome | Transient neurocognitive deficit after surgery using heart-lung machine |
1 | list | Familial amyloid cardiomyopathy | Transthyretin (TTR)-related familial amyloidotic cardiomyopathy is a hereditary TTR-related systemic amyloidosis (ATTR) with predominant cardiac involvement resulting from myocardial infiltration of abnormal amyloid protein |
1 | list | Crus fracture | Traumatic or pathological injury to the tibia in which the continuity of the bone is broken |
1 | list | Pott disease | Tuberculosis of the spine |
1 | list | Tufted angioma | Tufted angioma is a very rare, benign, cutaneous, slow-growing, vascular tumor mostly developing in infancy or early childhood |
1 | list | Meningioma | Tumor forms from meninges |
1 | list | Canine transmissible venereal tumor | Tumors most commonly seen on or near the genitalia. They are venereal, most likely transmitted through transplantation of cells by contact. Metastases have been reported. Spontaneous regression may occur. |
1 | list | Urogenital neoplasm | Tumors or cancer of the urogenital system in either the male or the female |
1 | list | Café au lait spot | Type of birthmark |
1 | list | Bronchopleural fistula | Type of fistula |
1 | list | Bruise | Type of hematoma |
1 | list | Psychogenic pain | Type of pain |
1 | list | Medical fetishism | Type of sexual fetish |
1 | list | Fear of missing out | Type of social anxiety |
1 | list | Shell shock | Type of trauma experienced in World War One |
1 | list | Oncovirus | Type of viruses |
1 | list | Peptic ulcer disease | Ulcer of an area of the gastrointestinal tract |
1 | list | Ullrich congenital muscular dystrophy | Ullrich congenital muscular dystrophy (UCMD) is characterized by early-onset, generalized and slowly progressive muscle weakness, multiple proximal joint contractures, marked hypermobility of the distal joints and normal intelligence |
1 | list | Nuchal cord | Umbilical chord wrapped around the fetus's neck in the womb |
1 | list | Umbilical cord ulceration and intestinal atresia | Umbilical cord ulceration-intestinal atresia syndrome is characterised by congenital intestinal atresia, umbilical cord ulceration and severe intrauterine haemorrhage |
1 | list | Anosognosia | Unawareness of one's own illness, symptoms or impairments |
1 | list | Uncombable hair syndrome | Uncombable hair syndrome (UHS), or pili trianguli et canaliculi, is a rare scalp hair shaft dysplasia |
1 | list | Urolithiasis | Urolithiasis |
1 | list | Intermenstrual bleeding | Uterine bleeding between menstrual periods |
1 | list | Vegetative-vascular dystonia | Vegetative-vascular dystonia |
1 | list | Oculofaciocardiodental syndrome | Very rare genetic disease involving ocular abnormalities and cardiac abnormalities. |
1 | list | Viet and Duc Nguyen | Vietnamese conjoined twins |
1 | list | Vitamin A deficiency | Vitamin A disease |
1 | list | Vulvar tumors | Vulvar tumors are those neoplasms of the vulva. |
1 | list | Vulvodynia | Vulvodynia is a chronic pain syndrome that affects the vulvar area and occurs without an identifiable cause. Symptoms typically include a feeling of burning or irritation. For the diagnosis to be made symptoms must last at least 3 months. |
1 | list | Wagner's disease | Wagner disease is a rare hereditary vitreoretinopathy characterized by an anomaleous vitreous associated with myopia, cataract, chorioretinal atrophy, and peripheral tractional or rhegmatogenous retinal detachment |
1 | list | Warm antibody autoimmune hemolytic anemia | Warm autoimmune hemolytic anemia is the most common form of autoimmune hemolytic anemia (see this term) defined by the presence of warm autoantibodies against red blood cells (autoantibodies that are active at temperatures between 37-40B0C) |
1 | list | Eosinophilic cellulitis | Wells syndrome is characterised by the presence of recurrent cellulitis-like eruptions with eosinophilia |
1 | list | Wiedemann–Rautenstrauch syndrome | Wiedemann-Rautenstrauch syndrome is a very rare disorder with features of premature aging recognizable at birth, decreased subcutaneous fat, hypotrichosis, relative macrocephaly and dysmorphism |
1 | list | Angioma | Wikimedia category |
1 | list | Serous cystadenoma | Wikipedia disambiguation page |
1 | list | Wildervanck syndrome | Wildervanck syndrome is characterized by the triad of cervical vertebral fusion (Klippel-Feil anomaly, see this term), bilateral abducens palsy with retracted eyes (Duane syndrome, see this term) and congenital perceptive deafness |
1 | list | Wolcott–Rallison syndrome | Wolcott-Rallison syndrome (WRS) is a very rare genetic disease, characterized by permanent neonatal diabetes mellitus (PNDM) with multiple epiphyseal dysplasia and other clinical manifestations, including recurrent episodes of acute liver failure |
1 | list | Woodhouse–Sakati syndrome | Woodhouse-Sakati syndrome is a multisystemic disorder characterized by hypogonadism, alopecia, diabetes mellitus, intellectual deficit and extrapyramidal signs with choreoathetoid movements and dystonia |
1 | list | Worster-Drought syndrome | Worster-Drought syndrome (WDS) is a form of cerebral palsy characterized by congenital pseudobulbar (suprabulbar) paresis manifesting as selective weakness of the lips, tongue and soft palate, dysphagia, dysphonia, drooling and jaw jerking |
1 | list | Adrenoleukodystrophy | X-linked adrenoleukodystrophy (X-ALD) is a peroxisomal disorder resulting in cerebral demyelination, axonal dysfunction in the spinal cord leading to spastic paraplegia, adrenal insufficiency and in some cases testicular insufficiency |
1 | list | Simpson–Golabi–Behmel syndrome | X-linked disease characterized by pre- and postnatal overgrowth and craniofacial, skeletal, cardiac and renal abnormalities |
1 | list | FG syndrome | X-linked disease characterized by retardation, hyperactivity, hypotonia, broad thumbs, big first toes and a characteristic facial appearance including macrocephaly and has an X-linked recessive inheritance pattern |
1 | list | Ogden syndrome | X-linked disease resulting from a deficiency in N-terminal acetyltransferase, extreme abrupt behavior, anger issues, characterized by postnatal growth failure with severe delays and dysmorphic features in boys |
1 | list | Haemophilia A | X-linked disease that has material basis in Factor VIII deficiency, which results in the formation of fibrin deficient clots which makes coagulation much more prolonged |
1 | list | Becker muscular dystrophy | X-linked recessive inherited disorder characterized by slowly progressive muscle weakness of the legs and pelvis |
1 | list | Yemenite deaf-blind hypopigmentation syndrome | Yemenite deaf-blind hypopigmentation syndrome is an exceedingly rare genetic disorder characterized by cutaneous pigmentation anomalies, ocular disorders and hearing loss |
1 | list | Young's syndrome | Young syndrome is characterised by the association of obstructive azoospermia with recurrent sinobronchial infections |
1 | list | Joseph and Luka Banda | Zambian conjioned twins |
1 | list | Zimmermann–Laband syndrome | Zimmermann-Laband syndrome (ZLS) is a rare disorder characterized by gingival fibromatosis, coarse facial appearance, and absence or hypoplasia of nails or terminal phalanges of hands and feet |
1 | list | Late talker | a child demonstrating speech ability later than is average |
1 | list | Pierre Robin sequence | a congenital condition with micrognathia and glossoptosis |
1 | list | Sick building syndrome | a medical condition where people in a building suffer from symptoms of illness or feel unwell for no apparent reason |
1 | list | Multiple drug resistance | a microbial organism's resistance to multiple antimicrobial drugs |
1 | list | Hybristophilia | a paraphilia in which sexual arousal are responsive to and contingent upon being with a partner known to have committed an outrage, cheating, lying, known infidelities, or crime |
1 | list | Rheumatoid nodule | a particular variant of polyarthritis associated with early manifestations of palindromic rheumatism, radiologic subchondral bone cysts, and subcutaneous rheumatoid nodules |
1 | list | Necrophilia | a pathological attraction to dead bodies, especially sexual attraction or intercourse |
1 | list | Substance abuse | a patterned use of a drug in which the user consumes the psychoactive/chemical substance substances in amounts or with methods which are harmful to themselves or others |
1 | list | Major depressive episode | a period characterized by the symptoms of major depressive disorder |
1 | list | Retrognathism | a physical misalignment of the jaw bones |
1 | list | Prediabetes | a predisease state of hyperglycemia with high risk for diabetes |
1 | list | Acidosis | a process causing increased acidity in the blood and other body tissues |
1 | list | Diffuse myelinoclastic sclerosis | a progressive demyelinating disorder of the central nervous system |
1 | list | Paternal depression | a psychological disorder derived from parental depression |
1 | list | Substance-induced psychosis | a psychosis that results from the effects of exogenous toxic substances or drugs |
1 | list | Adenylosuccinate lyase deficiency | a rare autosomal recessive metabolic disorder |
1 | list | Landau–Kleffner syndrome | a rare childhood neurological syndrome characterized by seizures and progressive loss of speech typically in a child with previous age-appropriate development |
1 | list | Chromhidrosis | a rare condition characterized by the secretion of colored sweat, caused by the deposition of lipofuscin in the sweat glands. Usually chromhidrosis affects the apocrine glands, mainly on the face and underarms. |
1 | list | Duane syndrome | a rare congenital disease characterized by external gaze palsy |
1 | list | Sturge–Weber syndrome | a rare congenital neurological and skin disorder associated with port-wine stains of the face, glaucoma, seizures, intellectual disability, and cerebral malformations and tumors. |
1 | list | Parry–Romberg syndrome | a rare disease characterized by progressive shrinkage and degeneration of the tissues beneath the skin, usually on only one side of the face (hemifacial atrophy) but occasionally extending to other parts of the body |
1 | list | Walker–Warburg syndrome | a rare form of autosomal recessive congenital muscular dystrophy. |
1 | list | Von Hippel–Lindau disease | a rare genetic disorder characterized by visceral cysts and benign tumors in multiple organ systems with potential for subsequent malignant change. |
1 | list | Pseudopseudohypoparathyroidism | a rare genetic disorder in the human body |
1 | list | Aicardi–Goutières syndrome | a rare genetic neurodevelopmental disorder |
1 | list | SUNCT syndrome | a rare headache disorder of trigeminal autonomic cephalalgia (TAC) category |
1 | list | Dejerine–Sottas disease | a rare hereditary neurological disorder characterised by damage to the peripheral nerves and resulting progressive muscle wasting |
1 | list | Rasmussen's encephalitis | a rare inflammatory neurological disease, characterized by frequent and severe seizures, loss of motor skills and speech, hemiparesis (weakness on one side of the body), encephalitis (inflammation of the brain), and dementia |
1 | list | Hoyeraal-Hreidarsson syndrome | a rare multisystem disease characterized by intrauterine growth retardation, microcephaly, cerebellar hypoplasia, progressive combined immune deficiency and aplastic anemia. |
1 | list | Epidermal nevus syndrome | a rare neurocutaneous syndrome |
1 | list | Bannayan–Riley–Ruvalcaba syndrome | a rare overgrowth syndrome and hamartomatous disorder with occurrence of multiple subcutaneous lipomas, macrocephaly and hemangiomas. |
1 | list | Lichen striatus | a rare skin condition, seen primarily in children, characterized by self-limiting eruption of small, scaly papules. |
1 | list | Gelastic seizure | a rare type of seizure that involves a sudden burst of energy, usually in the form of laughing or crying |
1 | list | Cogan syndrome | a rare vasculitis of children and young adults characterized by nonsyphilitic interstitial keratitis of cornea, fever and fatigue. |
1 | list | Primary familial brain calcification | a rare, genetic neurological disorder characterized by abnormal deposits of calcium in areas of the brain that control movement |
1 | list | Meckel syndrome | a rare, lethal, ciliopathic, genetic disorder with malformations of the urinary system, of central nervous system, hepatic developmental defects, and pulmonary hypoplasia. |
1 | list | Electromagnetic hypersensitivity | a sensitivity to electromagnetic fields, not recognized by medical science |
1 | list | Psychomotor agitation | a set of signs and symptoms that stem from mental tension and anxiety; еhe signs are unintentional and purposeless motions; the symptoms are emotional distress and restlessness |
1 | list | Hypokinetic diseases | a term sometimes given to selected diseases and other health conditions |
1 | list | Ankylosing spondylitis | a type of arthritis in which there is long term inflammation of the joints of the spine |
1 | list | Atonic seizure | a type of seizure that consists of partial or complete loss of muscle tone |
1 | list | Glioma | a type of tumor that starts in the brain or spine |
1 | list | Pipecolic acidemia | a very rare autosomal recessive metabolic disorder that is caused by a peroxisomal defect |
1 | list | Fazio–Londe disease | a very rare inherited motor neuron disease of children and young adults |
1 | list | Cenesthopathy | aberrant bodily sensation |
1 | list | Antimicrobial resistance | ability of a microbe to resist the effects of medication |
1 | list | Ergophobia | abnormal and persistent fear of work or fear of finding employment |
1 | list | Dysphagia lusoria | abnormal condition characterized by difficulty in swallowing caused by aberrant right subclavian artery |
1 | list | Nephroptosis | abnormal condition in which the kidney drops down into the pelvis when the patient stands up |
1 | list | Disease | abnormal condition negatively affecting organisms |
1 | list | Psychosis | abnormal condition of the mind that involves a loss of contact with reality |
1 | list | Fistula | abnormal connection between two hollow spaces (technically, two epithelialized surfaces), such as blood vessels, intestines, or other hollow organs |
1 | list | Afterdepolarization | abnormal depolarizations of cardiac myocytes |
1 | list | Dysplasia | abnormal development, at macroscopic or microscopical level |
1 | list | Megaesophagus | abnormal dilation of the esophagus not due to obstruction |
1 | list | Varicocele | abnormal enlargement of the pampiniform venous plexus in the scrotum |
1 | list | Ophidiophobia | abnormal fear of snakes |
1 | list | Astraphobia | abnormal fear of thunder and lightning |
1 | list | Lilapsophobia | abnormal fear of tornadoes or hurricanes |
1 | list | Gynophobia | abnormal fear of women |
1 | list | Carnosity | abnormal fleshy excrescence or tuberosity |
1 | list | Tumor | abnormal growth of tissue forming a mass |
1 | list | Atrial fibrillation | abnormal heart rhythm characterized by rapid and irregular beating |
1 | list | Multifocal atrial tachycardia | abnormal heart rhythm, specifically a type of supraventricular tachycardia |
1 | list | Splenomegaly | abnormal increased size of the spleen |
1 | list | Neoplasm | abnormal mass of tissue as a result of abnormal growth or division of cells |
1 | list | Pneumatosis | abnormal presence of air or other gas within tissues |
1 | list | Cemento-osseous dysplasia | abnormal production of bone in the mandible |
1 | list | Formication | abnormal sensation that bugs are crawling on or under the skin |
1 | list | Hyperprosexia | abnormal state of attention |
1 | list | Tooth discoloration | abnormal tooth color, hue or translucency |
1 | list | Hemoglobin Barts | abnormal type of hemoglobin that consists of four gamma globins |
1 | list | Leukocoria | abnormal white reflection from the retina of the eye |
1 | list | Pseudoathetosis | abnormal writhing movements, usually of the fingers, caused due to disruption in proprioception |
1 | list | Arteriovenous fistula | abnormal, epithelial-lined connection between an artery and vein that is present at the time of birth |
1 | list | Gerascophobia | abnormal, incessant fear and repulsement of growing older (ageing) due to loss of health amd ability. |
1 | list | Traumatophobia | abnormal, pathological fear of having an injury |
1 | list | Thrombophilia | abnormality of blood coagulation that increases the risk of thrombosis (blood clots in blood vessels) |
1 | list | Hyperlipidemia | abnormally elevated levels of lipids or lipoproteins in the blood |
1 | list | Supraventricular tachycardia | abnormally fast heart rhythm arising from improper electrical activity in the upper part of the heart |
1 | list | Azotemia | abnormally high levels of nitrogen in the blood |
1 | list | Neutropenia | abnormally low concentration of neutrophils in the blood |
1 | list | Eosinopenia | abnormally low level of eosinophils in the blood |
1 | list | Acute kidney injury | abrupt loss of kidney function that develops within 48 hours |
1 | list | Brain abscess | abscess caused by inflammation and collection of infected material in the brain |
1 | list | Anencephaly | absence of a major portion of the brain, skull, and scalp that occurs during embryonic development |
1 | list | Amenorrhea | absence of a menstrual period in a woman of reproductive age |
1 | list | Amazia | absence of the mammary gland |
1 | list | Aphalangia | absence of the phalanx bone on one or more digits |
1 | list | Asystole | absence of ventricular contractions lasting longer than the minimum possible to sustain life |
1 | list | Aboulia | absence of willpower or decisiveness, especially as a symptom of mental disorder |
1 | list | Atheroma | accumulation of degenerative material in the inner layer of artery walls |
1 | list | Pleural effusion | accumulation of excess fluid in the pleural cavity |
1 | list | Achondrogenesis type 1B | achondrogenesis that has material basis in mutation in the SLC26A2 gene which results in umbilical or inguinal hernia and a prominent rounded abdomen |
1 | list | Achondrogenesis type 2 | achondrogenesis that has material basis in mutations in the COL2A1 gene which results in underdeveloped lungs, hydrops fetalis, a prominent forehead and abnormal ossification of the located in vertebral column or located in pelvis |
1 | list | Chronic inflammatory demyelinating polyneuropathy | acquired immune-mediated inflammatory disorder of the peripheral nervous system |
1 | list | Hyperuricemia | acquired metabolic disease that has material basis in an abnormally high level of uric acid in the blood. |
1 | list | Lactic acidosis | acquired metabolic disease that has material basis in low pH in body tissues and blood accompanied by the buildup of lactate especially D-lactate |
1 | list | Hyperprolactinaemia | acquired metabolic disease that has material basis in the presence of abnormally-high levels of prolactin in the blood |
1 | list | Amyloidosis | acquired metabolic disease that involves abnormal deposited of amyloid proteins in organs and/or tissues |
1 | list | Carpenter syndrome | acrocephalosyndactylia characterized by craniosynostosis, acrocephaly, obesity, syndactyly and polydactyly |
1 | list | Saethre–Chotzen syndrome | acrocephalosyndactylia that has material basis in a genetic mutation in the TWIST1 gene which results in premature fusion located in skull |
1 | list | Greig cephalopolysyndactyly syndrome | acrocephalosyndactylia that has material basis in mutation in the GLI3 gene which results in abnormal development located in limb, located in head, located in face |
1 | list | Pfeiffer syndrome | acrocephalosyndactylia that has material basis in mutations in the FGFR1 and FGFR2 gene which results in premature fusion located in skull |
1 | list | Nager acrofacial dysostosis | acrofacial dysostosis characterized by underdeveloped cheek bones, very small lower jaw, cleft palate, defects in the middle ear, absent eyelashes, and a notch in the lower eyelids called a coloboma, in children |
1 | list | Exhibitionism | act of exposing in a public or semi-public context those parts of one's body that are not normally exposed |
1 | list | Alcohol enema | act of introducing alcohol into the rectum and colon via the anus |
1 | list | Opioid overdose | acute condition due to excessive opioids |
1 | list | Hepatitis A | acute infectious disease of the liver |
1 | list | Acute lung injury | acute lung injury |
1 | list | Acute promyelocytic leukemia | acute myeloid leukemia characterized by accumulation of promyelocytes in the bone marrow and by a translocation between chromosomes 15 and 17 |
1 | list | Acute panmyelosis with myelofibrosis | acute myeloid leukemia characterized by bone marrow fibrosis without preexisting primary myelofibrosis |
1 | list | Bouffée délirante | acute polymorphic psychotic disorder (bouffée délirante) |
1 | list | Erythropoietic protoporphyria | acute porphyria characterized by a deficiency in the enzyme ferrochelatase, leading to abnormally high levels of protoporphyrin in the tissue |
1 | list | Porphyria cutanea tarda | acute porphyria characterized by painful, blistering skin lesions that develop on sun-exposed skin |
1 | list | Oneirophrenia | acute schizophrenia-like psychotic disorder in which hallucinations and dream-like state are the main clinical features |
1 | list | Combat stress reaction | acute stress disorder that involves neurotic reactions to unusual, severe, or overwhelming military stress |
1 | list | Video game addiction | addiction to computer and video games |
1 | list | Supernumerary nipple | additional nipple occurring in mammals |
1 | list | Cystadenocarcinoma | adenocarcinoma that derives from epithelial cells originating in glandular tissue, in which cystic accumulations of retained secretions are formed |
1 | list | Papillary adenocarcinoma | adenocarcinoma that derives from epithelial cells originating in glandular tissue, which form complex papillary structures and exhibit compressive, destructive growth that replaces the normal tissue |
1 | list | Signet ring cell carcinoma | adenocarcinoma that derives from epithelial cells originating in glandular tissue, which have signet ring appearance |
1 | list | Clear-cell adenocarcinoma | adenocarcinoma that derives from epithelial cells which have clear cytoplasm |
1 | list | Hepatoid tumor | adenocarcinoma with morphologic characteristics similar to hepatocellular carcinoma, arising from an anatomic site other than the liver |
1 | list | Nipple adenoma | adenoma that involves the nipple |
1 | list | Cystadenoma | adenoma that is a cystic |
1 | list | Insulinoma | adenoma that is located in the pancreas and is characterized by overproduction of insulin |
1 | list | Asherman's syndrome | adhesions or fibrosis of endometrium of uterus |
1 | list | Juvenile myoclonic epilepsy | adolescence-adult electroclinical syndrome that is characterized by brief, involuntary twitching of a muscle or a group of muscles (myoclonus) early in the morning with onset between 12 and 18 years |
1 | list | Primary aldosteronism | adrenal adenoma characterized by over production of aldosterone |
1 | list | Adrenocortical adenoma | adrenal adenoma that is a benign tumor of the adrenal cortex |
1 | list | Adrenocortical carcinoma | adrenal cortex cancer that forms in the outer layer of tissue of the adrenal gland and that has material basis in abnormally proliferating cells derives from epithelial cells |
1 | list | Primary pigmented nodular adrenocortical disease | adrenal cortex disease characterized by small to normal sized adrenal glands containing multiple small cortical pigmented nodules |
1 | list | X-linked adrenal hypoplasia congenita | adrenal cortical hypofunction that is characterized by a reduction in adrenal gland function resulting from incomplete development of the adrenal cortex and has material basis in the nuclear receptor NR0B1 (DAX1) gene |
1 | list | Addison's disease | adrenal cortical hypofunction that is characterized by insufficient steroid hormone production by the adrenal glands. |
1 | list | Waterhouse–Friderichsen syndrome | adrenal gland disease that is characterized by failure of the adrenal gland due to bleeding into the gland |
1 | list | Hyperaldosteronism | adrenal gland hyperfunction disease that results in the overproduction of aldosterone by the adrenal glands |
1 | list | Cushing's syndrome | adrenal gland overactivity caused by a tumor of the pituitary gland or by medication |
1 | list | Drug eruption | adverse drug reaction of the skin |
1 | list | Cubitus varus | affecting the elbow |
1 | list | Pallor mortis | after-death paleness that occurs in those with light/white skin |
1 | list | Stargardt disease | age related macular degeneration that is characterized by progressive vision loss usually to the point of legal blindness |
1 | list | Alexithymia | agnosia that is a deficiency in understanding, processing, or describing emotions |
1 | list | Akinetopsia | agnosia that is a loss of motion perception |
1 | list | Finger agnosia | agnosia that is a loss of the ability to distinguish the fingers on the hand |
1 | list | Apperceptive agnosia | agnosia that is a loss of the ability to distinguish visual shapes |
1 | list | Auditory agnosia | agnosia that is a loss of the ability to distinguishing environmental and non-verbal auditory cues including difficulty distinguishing speech from non-speech sounds even though hearing is usually normal |
1 | list | Integrative agnosia | agnosia that is a loss of the ability to integrate these elements together into comprehensible perceptual wholes while recognizing elements of the whole |
1 | list | Apraxia | agnosia that is a loss of the ability to map out physical actions in order to repeat them in functional activities |
1 | list | Pain asymbolia | agnosia that is a loss of the ability to perceive and process pain |
1 | list | Cortical deafness | agnosia that is a loss of the ability to perceive any auditory information but whose hearing is intact |
1 | list | Social-emotional agnosia | agnosia that is a loss of the ability to perceive facial expression, body language and intonation, rendering them unable to non-verbally perceive people's emotions and limiting that aspect of social interaction |
1 | list | Simultanagnosia | agnosia that is a loss of the ability to recgonize a whole image or scene while retaining the ability to recognize objects or details in their visual field one at a time |
1 | list | Auditory verbal agnosia | agnosia that is a loss of the ability to recognising spoken words as semantically meaningful |
1 | list | Cerebral achromatopsia | agnosia that is a loss of the ability to recognize a color, while being able to perceive or distinguish it |
1 | list | Phonagnosia | agnosia that is a loss of the ability to recognize familiar voices |
1 | list | Amusia | agnosia that is a loss of the ability to recognize musical notes, rhythms, and intervals |
1 | list | Associative visual agnosia | agnosia that is a loss of the ability to recognize visual scenes or classes of objects but retain the abilty to describe them |
1 | list | Topographical disorientation | agnosia that is a loss of the ability to rely on visual cues to guide them directionally due to the inability to recognise objects |
1 | list | Astereognosis | agnosia that is the loss of the ability to recognize objects by touch based on its texture, size and weight |
1 | list | Stadtaffe | album |
1 | list | Alcohol use among college students | alcohol consumption by students |
1 | list | Blackout (drug-related amnesia) | alcohol-related amnesia |
1 | list | Major depressive disorder | all-encompassing low mood accompanied by low self-esteem, and by loss of interest or pleasure in normally enjoyable activities. |
1 | list | Oculolinctus | alleged eyeball-licking fetish |
1 | list | Sluggish schizophrenia | alleged mental disorder applied to Soviet political dissidents |
1 | list | Nickel allergy | allergic contact dermatitis that has allergic trigger nickel atom |
1 | list | Oral allergy syndrome | allergic reaction in the mouth following eating food |
1 | list | African blackwood dermatitis | allergic skin reaction to a particular type of wood |
1 | list | Sweat allergy | allergy associated with the production of sweat |
1 | list | Wheat allergy | allergy involving a FOODON:00001141 |
1 | list | ATR-16 syndrome | alpha thalassemia that has material basis in a deletion in chromosome 16p that involves the alpha-1 (HBA1) and alpha-2 (HBA2) genes, among others |
1 | list | Hemoglobin H disease | alpha thalassemia that has material basis in contiguous gene deletion of the hemoglobin alpha-1 (HBA1) and alpha-2 (HBA2) genes on one chromosome 16, and a defect, deletional or nondeletional, in either HBA1 or HBA2 on the other |
1 | list | Alpha-thalassemia mental retardation syndrome | alpha thalassemia that has material basis in mutation in the ATRX gene on Xq21 |
1 | list | Swimming-induced pulmonary edema | also known as swimming-induced pulmonary edema |
1 | list | Microvasculature remodeling | alterations of vascular wall structures, often leading to elevated vascular resistance |
1 | list | Enamel-renal syndrome | amelogenesis imperfecta that has material basis in homozygous or compound heterozygous mutation in the FAM20A gene on chromosome 17q24 |
1 | list | Cystathioninuria | amino acid metabolic disorder characterized by elevated plasma and urinary cystathionine levels that has material basis in homozygous or compound heterozygous mutation in the CTH gene on chromosome 1p31 |
1 | list | Brunner syndrome | amino acid metabolic disorder characterized by recessive X-linked inhetiance, impaired monoamine metabolism, impulsive aggressiveness and mild mental retardation that has material basis in mutation in the MAOA gene on chromosome location Xp11 |
1 | list | Organic acidemia | amino acid metabolic disorder that disrupts normal amino acid metabolism causing a building up of branched-chain amino acids |
1 | list | Ornithine translocase deficiency | amino acid metabolic disorder that has material basis in deficiency of ornithine translocase resulting in the accumulation of ammonia in the blood |
1 | list | Glycine encephalopathy | amino acid metabolic disorder that involves abnormally high levels of the amino acid glycine in bodily fluids and tissues |
1 | list | Carbamoyl phosphate synthetase I deficiency | amino acid metabolic disorder that involves accumulation of ammonia in the blood |
1 | list | Hyperlysinemia | amino acid metabolic disorder that involves an abnormal increase of lysine in the blood |
1 | list | Hyperhomocysteinemia | amino acid metabolic disorder that involves an abnormally large level of homocysteine in the blood |
1 | list | Homocystinuria | amino acid metabolic disorder that involves an accumulation of homocysteine in the serum and an increased excretion of homocysteine in the urine |
1 | list | Systemic primary carnitine deficiency | amino acid metabolic disorder that involves defective proteins called carnitine transporters, which bring carnitine into cells and prevent its escape from the body preventing the body cannot utilize fats for energy |
1 | list | Multiple carboxylase deficiency | amino acid metabolic disorder that involves failures of carboxylation enzymes |
1 | list | Tyrosinemia | amino acid metabolic disorder that involves impaired break down of the amino acid tyrosine |
1 | list | Alkaptonuria | amino acid metabolic disorder that involves phenylalanine and tyrosine metabolism with the accumulation of homogentisic acid, a toxic tyrosine byproduct |
1 | list | Argininosuccinic aciduria | amino acid metabolic disorder that involves the accumulation of argininosuccinic acid (ASA) in the blood and urine |
1 | list | Cystinuria | amino acid metabolic disorder that involves the formation of cystine stones in the kidneys, ureter, and bladder |
1 | list | 2-Hydroxyglutaric aciduria | amino acid metabolic disorder that is an autosomal recessive neurometabolic disorder characterized by the significant elevation of urinary levels of hydroxyglutaric acid causing progressive brain damage |
1 | list | Phenylketonuria | amino acid metabolic disorder that is characterized by a mutation in the gene for the hepatic enzyme phenylalanine hydroxylase (PAH), rendering it nonfunctional |
1 | list | Transient global amnesia | amnestic disorder that is characterized by temporary but almost total disruption of short-term memory with a range of problems accessing older memories. |
1 | list | Primary cutaneous amyloidosis | amyloidosis characterized by pruritus, skin scratching and by deposits of amyloid in the dermis |
1 | list | Cerebral amyloid angiopathy | amyloidosis where amyloid protein progressively deposits in cerebral blood vessel walls with subsequent degenerative vascular changes that usually result in spontaneous cerebral hemorrhage, ischemic lesions and progressive dementia |
1 | list | Nonverbal autism | an Autism Spectrum Disorder |
1 | list | Panic disorder | an anxiety disorder characterized by unexpected and repeated episodes of intense fear accompanied by physical symptoms |
1 | list | Phobia | an anxiety disorder defined by a persistent and excessive fear of an object or situation |
1 | list | Lambert–Eaton myasthenic syndrome | an autoimmune, presynaptic disorder of neuromuscular transmission characterized by fluctuating muscle weakness and autonomic dysfunction frequently associated with small-cell lung cancer (SCLC) |
1 | list | Nevoid basal-cell carcinoma syndrome | an autosomal dominant condition that can cause unusual facial appearances and a predisposition for basal-cell carcinoma |
1 | list | Binge eating disorder | an eating disorder characterized by frequent and recurrent binge eating episodes with associated negative psychological and social problems, but without subsequent purging episodes |
1 | list | Culture shock | an experience one may have when moving to a cultural environment which is different from one's own |
1 | list | Febrile infection-related epilepsy syndrome | an explosive-onset, potentially fatal acute epileptic encephalopathy that develops in previously healthy children and adolescents following the onset of a non-specific febrile illness |
1 | list | Osteopetrosis | an extremely rare inherited disorder whereby the bones harden, becoming denser, sometimes causing bones to dissolve and break, caused by malfunctioning osteoclasts’ inability to resorb bone |
1 | list | Idée fixe (psychology) | an idea that preoccupies an individual and that he is unwilling to give up despite evidence to the contrary |
1 | list | Smith–Lemli–Opitz syndrome | an inborn error of cholesterol synthesis. It is an autosomal recessive, multiple malformation syndrome caused by a mutation in the enzyme 7-Dehydrocholesterol reductase, or DHCR7. |
1 | list | Pentosuria | an inborn error of metabolism characterized by the excretion of 1 to 4 g of the pentose L-xylulose in the urine per day |
1 | list | Stye | an infection of an oil gland in the eyelid. This results in a red tender bump at the edge of the eyelid. The outside or the inside of the eyelid can be affected |
1 | list | Transverse myelitis | an inflammatory demyelinating disorder of the spinal cord, either idiopathic or secondary to a known cause |
1 | list | Myokymia | an involuntary, spontaneous, localised quivering of a few muscles, or bundles within a muscle, but which are insufficient to move a joint |
1 | list | High-functioning autism | an obsolete label applying to autistic people with an IQ of 70 or above |
1 | list | CD30+ cutaneous T-cell lymphoma | anaplastic lymphoma of the skin which develops as a primary neoplasm expressing the CD30 antigen |
1 | list | Right-sided aortic arch | anatomic abnormality that occurs during embryonic development, in which the aortic arch is right-sided |
1 | list | Hua–Yi distinction | ancient Chinese concept that differentiated a culturally defined "China" (called Hua, Huaxia 華夏, or Xia 夏) from cultural or ethnic outsiders (Yi "barbarians") |
1 | list | Iron-deficiency anemia | anemia caused by a lack of iron |
1 | list | Aplastic anemia | anemia that is characterized by a deficiency of red blood cells, white blood cells and platelets produced by bone marrow |
1 | list | Microvascular angina | angina (chest pain) with signs associated with decreased blood flow to heart tissue but with normal coronary arteries |
1 | list | White elephant (animal) | animal |
1 | list | Melanism | animal phenotype |
1 | list | Bosworth fracture | ankle fracture |
1 | list | Depersonalization | anomaly of self-awareness |
1 | list | Vaccine shedding | anti-vaccine myth |
1 | list | Anal fistula | anus disease characterized by is an abnormal connection between the epithelialised surface of the anal canal and the perianal skin |
1 | list | Mathematical anxiety | anxiety about one's ability to do mathematics |
1 | list | Fear of trains | anxiety and fear associated with trains, railways and railway travel |
1 | list | Death anxiety (psychology) | anxiety caused by thoughts of death |
1 | list | Selective mutism | anxiety disorder |
1 | list | Workplace phobia | anxiety disorder and specific phobia associated with workspace |
1 | list | Separation anxiety disorder | anxiety disorder that involves the feeling of excessive and inappropriate levels of anxiety over being separated from a person to whom the individual has a strong emotional attachment or place |
1 | list | Obsessive–compulsive disorder | anxiety disorder that involves unwanted and repeated thoughts, feelings, ideas, sensations (obsessions), or behaviors that make them feel driven to do something (compulsions) |
1 | list | Generalized anxiety disorder | anxiety disorder that is characterized by long-lasting anxiety that is not focused on any one object or situation |
1 | list | Numerophobia | anxiety disorder, where the condition is fear of dealing with numbers or mathematics |
1 | list | School refusal | anxiety or fear of school causing physical symptoms such as nausea and headaches |
1 | list | Dysautonomia | any disease or malfunction of the autonomic nervous system |
1 | list | Notifiable disease | any disease that is required by law to be reported to government authorities |
1 | list | Immersion foot syndromes | any of several skin conditions affecting the feet |
1 | list | Abdominal aortic aneurysm | aortic aneurysm that is located in the abdominal aorta |
1 | list | Thoracic aortic aneurysm | aortic aneurysm that is located in the thoracic aorta |
1 | list | Aortic stenosis | aortic valve disease that has physical basis in incomplete opening of the aortic valve |
1 | list | Aortic insufficiency | aortic valve disease that is characterized by leaking of the aortic valve of the heart causes blood to flow in the reverse direction during ventricular diastole, from the aorta into the left ventricle |
1 | list | Myelophthisic anemia | aplastic anemia that is characterized by displacement of hemopoietic bone-marrow tissue either by fibrosis, tumors or granulomas |
1 | list | Sideroblastic anemia | aplastic anemia where the bone marrow produces ringed sideroblasts rather than healthy red blood cells (erythrocytes) |
1 | list | False pregnancy | appearance of clinical or subclinical signs and symptoms associated with pregnancy when the woman is not actually pregnant |
1 | list | Caput medusae | appearance of distended and engorged superficial epigastric veins |
1 | list | Pseudomyxoma peritonei | appendix cancer that is characterized by progressive accumulation of mucus-secreting tumor cells within the abdomen and pelvis |
1 | list | Cavitation (bone) | area of dead bone caused by a lack of blood flow |
1 | list | Osteonecrosis of the jaw | area of necrotic bone in the mandible or maxilla |
1 | list | Zettai ryōiki | area of the thigh delimited by high socks and a short skirt or shorts |
1 | list | Limb infarction | area of tissue death of an arm or leg |
1 | list | Pyogenic liver abscess | areas of pus from bacterial infection in the hepatic parenchyma |
1 | list | Uhl anomaly | arrhythmogenic right ventricular dysplasia that has material basis in heterozygous mutation in the TGFB3 gene on chromosome 14q24 |
1 | list | Arsenic poisoning | arsenic affecting human life |
1 | list | 1858 Bradford sweets poisoning | arsenic poisoning in United Kingdom |
1 | list | ACDC (medicine) | arterial calcification due to deficiency of CD73, rare genetic disorder that causes calcium buildup in the arteries and joints of the hands and feet, and other areas below the waist |
1 | list | Cerebral arteriovenous malformation | arteriovenous malformation that is located in the brain |
1 | list | Peripheral artery disease | artery disease characterized by build up of plaque in the arteries that carry blood to your head, organs, and limbs |
1 | list | Coronary artery disease | artery disease characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles |
1 | list | Cerebrovascular disease | artery disease that is characterized by dysfunction of the blood vessels supplying the brain |
1 | list | Oligoarthritis | arthritis affecting two to four joints |
1 | list | Chondrocalcinosis | arthritis that has material basis in the accumulation of salt crystals located in joint |
1 | list | Septic arthritis | arthritis that involves infection by a pathogen located in joint |
1 | list | Adult-onset Still's disease | arthritis that is a rare from of inflammatory arthritis characterized by fevers, rash, and joint pain |
1 | list | Reactive arthritis | arthritis that is an autoimmune disease which develops due to an infection located elsewhere in the body |
1 | list | Pneumonoultramicroscopicsilicovolcanoconiosis | artificial word for a lung disease, longest English word published in a dictionary |
1 | list | Allergic bronchopulmonary aspergillosis | aspergillosis that involves an allergic reaction due to the spores of Aspergillus moulds (A. fumigatus), which colonizes the mucus in the airways causing inflammation |
1 | list | Conorenal syndrome | asphyxiating thoracic dystrophy that has material basis in homozygous or compound heterozygous mutation in the IFT140 gene on chromosome 16p13 |
1 | list | Pregnancy category | assessment given to a medication based on the potential danger to a fetus |
1 | list | Syndrome | association of several clinically recognizable features |
1 | list | Fibrillary astrocytoma | astrocytoma that is characterized as a low grade astrocytoma and has material basis in neoplastic astrocytes |
1 | list | Pilocytic astrocytoma | astrocytoma that is characterized by cells that look like fibers when viewed under a microscope and is located in the brain |
1 | list | Anaplastic astrocytoma | astrocytoma that is characterized by cells with regular, round to oval nuclei |
1 | list | Aberrations of the eye | asymmetries in the topography and refractive index of the corneal surface that affect visual acuity |
1 | list | Familial atrial fibrillation | atrial fibrillation that has material basis in autosomal dominant inheritance of the familial atrial fibrillation (ATFB) genes |
1 | list | Geographic tongue | atrophic glossitis that is characterized as an inflammatory condition of the mucous membrane of the tongue, usually on the dorsal surface |
1 | list | Cerebellar degeneration | atrophy (wasting) of the cerebellum |
1 | list | Encephalitis lethargica | atypical form of encephalitis |
1 | list | Nonsyndromic deafness | auditory system disease that is associated with permanent hearing loss caused by damage to structures in the inner ear and/or the middle ear, which is not associated with other signs and symptoms |
1 | list | Atypical autism | autism spectrum disorder that involves some autistic symptoms occuring after age 3 with an abscence of all the traits necessary for a diagnosis of autism |
1 | list | Hashimoto's thyroiditis | autoimmune disease |
1 | list | Granulomatosis with polyangiitis | autoimmune disease affecting blood vessels in the lungs, kidneys, and skin |
1 | list | Autoimmune hemolytic anemia | autoimmune disease of blood that is characterized by deficient red blood cells caused by auto-antibodies. |
1 | list | Autoimmune polyendocrine syndrome | autoimmune disease of endocrine system characterized by abnormal functioning of the immune system that causes auto-reactivity against endocrine organs |
1 | list | Autoimmune thyroiditis | autoimmune disease of endocrine system that involves inflammation located in thyroid gland caused by the immune system reacting against its own tissues |
1 | list | Autoimmune pancreatitis | autoimmune disease of endocrine system that is located in the pancreas |
1 | list | Autoimmune hepatitis | autoimmune disease of gastrointestinal tract that results in inflammation located in liver caused by the body's immune system attacking the liver cells |
1 | list | Bullous pemphigoid | autoimmune disease of skin and connective tissue characterized by large blisters |
1 | list | Guillain–Barré syndrome | autoimmune disease that causes the immune system to attack part of the peripheral nervous system |
1 | list | Caspase-8 deficiency | autoimmune lymphoproliferative syndrome that has material basis in homozygous mutation in the CASP8 gene on chromosome 2q33 |
1 | list | Autoimmune polyendocrine syndrome type 1 | autoimmune polyendocrine syndrome that is inherited in an autosomal recessive fashion, which is characterized by abnormal functioning of the immune system that causes auto-reactivity against endocrine organs |
1 | list | Waardenburg syndrome | autosomal disease characterized by varying degrees of deafness, minor defects in structures arising from the neural crest and pigmentation anomalies of the hair, the skin and/or the iris of both eyes |
1 | list | Machado–Joseph disease | autosomal dominant cerebellar ataxia that is characterized by slow degeneration of the hindbrain and has material basis in expansion of CAG triplet repeats (glutamine) in the ATXN3 gene |
1 | list | CADASIL | autosomal dominant cerebrovascular disorder characterized by recurrent subcortical ischemic stroke and cognitive impairment |
1 | list | Marcus Gunn phenomenon | autosomal dominant condition with incomplete penetrance, in which nursing infants will have rhythmic upward jerking of their upper eyelid |
1 | list | Rapp–Hodgkin syndrome | autosomal dominant disease characterized by abnormal development of ectodermal tissues including the skin, hair, nails, teeth and sweat glands and anhidrotic ectodermal dysplasia with cleft lip/palate |
1 | list | Axenfeld syndrome | autosomal dominant disease characterized by abnormalities of the front part of the eye, the anterior segment |
1 | list | Holt–Oram syndrome | autosomal dominant disease characterized by congenital anomalies located_in heart and located_in upper limb. |
1 | list | Ectrodactyly–ectodermal dysplasia–cleft syndrome | autosomal dominant disease characterized by ectrodactyly, ectodermal dysplasia, and orofacial clefts (cleft lip-palate) |
1 | list | Li–Fraumeni syndrome | autosomal dominant disease characterized by increases risk of developing several types of cancer, including breast cancer, osteosarcomata and soft tissue sarcomata |
1 | list | Multiple endocrine neoplasia type 2 | autosomal dominant disease characterized by medullary carcinoma of the thyroid, pheochromocytoma, hyperparathyroidism, and occasionally cutaneous lichen amyloidosis |
1 | list | Multiple endocrine neoplasia type 2B | autosomal dominant disease characterized by medullary thyroid carcinoma, pheochromocytoma, multiple mucosal neuromas and intestinal ganglioneuromas, and often a marfanoid habitus and other skeletal abnormalities |
1 | list | Carney complex | autosomal dominant disease characterized by myxomas, spotty pigmentation of the skin and endocrine overactivity |
1 | list | Papillorenal syndrome | autosomal dominant disease characterized by optic nerve coloboma and renal disease that has material basis in heterozygous mutation in the PAX2 gene on chromosome 10q24 |
1 | list | Severe achondroplasia with developmental delay and acanthosis nigricans | autosomal dominant disease characterized by severe achondroplasia, developmental delay and acanthosis nigricans that has material basis in heterozygous mutation in the FGFR3 gene on chromosome 4p16 |
1 | list | Hereditary hemorrhagic telangiectasia | autosomal dominant disease characterized by tarteriovenous malformations that lack intervening capillaries and result in direct connections between arteries and veins |
1 | list | Hereditary breast–ovarian cancer syndrome | autosomal dominant disease characterized by the higher than normal tendency to develop breast and ovarian cancers in genetically related families |
1 | list | Duane-radial ray syndrome | autosomal dominant disease characterized by upper limb anomalies, ocular anomalies, and, in some cases, renal anomalies and that has material basis in heterozygous mutation in the SALL4 gene on chromosome 20q13 |
1 | list | Feingold syndrome | autosomal dominant disease characterized by variable combinations of microcephaly, limb malformations, esophageal and duodenal atresias, and learning disability/mental retardation |
1 | list | Multiple endocrine neoplasia type 1 | autosomal dominant disease that has material basis in a mutation in the MEN1 tumor suppressor gene and is characterized by over active endocrine glands frequently involving tumors of the parathyroid glands, the pituitary gland, and the pancreas |
1 | list | Polyostotic fibrous dysplasia | autosomal dominant disease that involves skin pigmentation, bone and hormonal problems along with premature puberty |
1 | list | Larsen syndrome | autosomal dominant disease that is characterized by large-joint dislocations and characteristic craniofacial abnormalities |
1 | list | Branchio-oculo-facial syndrome | autosomal dominant disease that is characterized by low birth weight and growth retardation, bilateral branchial clefts |
1 | list | Juvenile polyposis syndrome | autosomal dominant disease that is characterized by predisposition to hamartomatous benign polyps in the gastrointestinal tract, specifically in the stomach, small intestine, colon, and rectum |
1 | list | Familial adenomatous polyposis | autosomal dominant disease that is has material basis in mutations in the APC gene and involves formation of numerous polyps in the epithelium of the large intestine which are initially benign and later transform into colon cancer |
1 | list | Hyperimmunoglobulin E syndrome | autosomal dominant form called Job's syndrome or Buckley syndrome, is a heterogeneous group of immune disorders |
1 | list | Peutz–Jeghers syndrome | autosomal dominant genetic disorder characterized by the development of benign hamartomatous polyps in the gastrointestinal tract and hyperpigmented macules on the lips and oral mucosa (melanosis) |
1 | list | Branchio-oto-renal syndrome | autosomal dominant genetic disorder involving the kidneys, ears, and neck |
1 | list | Hand-foot-genital syndrome | autosomal dominant human genetic disease characterized by limb malformations (e.g. bilateral shortening of thumbs/big toes) and urogenital defects (e.g. abnormalities of ureters/urethra; incomplete Müllerian fusion in females; hypospadias in males) |
1 | list | Weill–Marchesani syndrome | autosomal genetic disease characterized by short stature, bachycephaly and other facial abnormalities, brachydactyly, joint stiffness and distinctive ocular abnormalities |
1 | list | Septo-optic dysplasia | autosomal genetic disease characterized by the classical triad of optic nerve hypoplasia, pituitary gland hypoplasia and midline brain defects that has material basis in mutation in the HESX1 gene on chromosome 3p14 |
1 | list | Oculocutaneous albinism | autosomal recessive disease characterized by abnormal pigmentation of the skin, hair and eyes |
1 | list | Carvajal syndrome | autosomal recessive disease characterized by autosomal recessive inheritance of dilated cardiomyopathy, woolly hair, and keratoderma that has material basis in homozygous mutation in the DSP gene on chromosome 6p24 |
1 | list | 3-M syndrome | autosomal recessive disease characterized by dwarfism, facial dysmorphia and skeletal abnormalities |
1 | list | Seckel syndrome | autosomal recessive disease characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability |
1 | list | Galloway Mowat syndrome | autosomal recessive disease characterized by is a rare autosomal recessive disease, characterized by microcephaly with brain anomalies including CA in some cases, intellectual disability, and early-infantile-onset nephrotic syndrome |
1 | list | Schwartz–Jampel syndrome | autosomal recessive disease characterized by neuromyotonia and chondrodysplasia that has material basis in hypomorphic mutations in the HSPG2 gene on chromosome 1p36 |
1 | list | Chédiak–Higashi syndrome | autosomal recessive disease characterized by oculocutaneous albinism, immune deficiency, coagulation deficiency and neuropathy; it is that has material basis in mutations in the CHS1 gene |
1 | list | UV-sensitive syndrome | autosomal recessive disease characterized by photosensitivity and liver spots (solar lentigines) |
1 | list | Micro syndrome | autosomal recessive disease characterized by severe intellectual disability, microcephaly, congenital cataract, microcornea, microphthalmia, agenesis or hypoplasia of the corpus callosum and hypogenitalism |
1 | list | Griscelli syndrome | autosomal recessive disease characterized by silvery gray sheen of the hair and hypopigmentation of the skin |
1 | list | Epidermolysis bullosa simplex with muscular dystrophy | autosomal recessive disease characterized early childhood onset of progressive muscular dystrophy and blistering skin changes and that has material basis in homozygous or compound heterozygous mutation in the PLEC gene on chromosome 8q24 |
1 | list | Antley–Bixler syndrome | autosomal recessive disease that is characterized at birth or prenatally by malformations and deformities affecting the majority of the skeleton and other areas of the body with autosomal recessive inheritance of the FGFR2 gene |
1 | list | Xeroderma pigmentosum | autosomal recessive disease that is characterized by a deficiency in the ability to repair ultraviolet damage that has material basis in autosomal recessive inheritance of DNA repair |
1 | list | ABCD syndrome | autosomal recessive disease that is characterized by albinism, black lock, cell migration disorder of the neurocytes of the gut and sensorineural deafness and has material basis in a mutation in the endothelin B receptor gene (EDNRB) |
1 | list | Urofacial syndrome | autosomal recessive disease that is characterized by inverted facial expressions in association with a severe and early-onset form of dysfunctional urinary voiding |
1 | list | Cystic fibrosis | autosomal recessive disease that is characterized by the buildup of thick, sticky mucus that can damage many organs. |
1 | list | Sotos syndrome | autosomal recessive disease that occurs rarely and is characterized by excessive physical growth during the first 2 to 3 years of life |
1 | list | CANDLE syndrome | autosomal recessive disorder |
1 | list | Sjögren–Larsson syndrome | autosomal recessive form of ichthyosis apparent at birth |
1 | list | Cerebrotendineous xanthomatosis | autosomal recessive form of xanthomatosis. |
1 | list | Senior–Løken syndrome | autosomal recessive genetic disease characterized by progressive wasting of the filtering unit of the kidney (nephronophthisis), with or without medullary cystic renal disease, and progressive eye disease |
1 | list | Lysosomal acid lipase deficiency | autosomal recessive inborn error of metabolism that results in the body not producing enough active lysosomal acid lipase (LAL) enzyme |
1 | list | Niemann–Pick disease, type C | autosomal recessive lipid storage disorder that is characterized by accumulation of cholesterol and sphingomyelins in cells of the viscera and the central nervous system |
1 | list | Salla disease | autosomal recessive lysosomal storage disease |
1 | list | Glycogen storage disease type II | autosomal recessive metabolic disorder |
1 | list | Lucey–Driscoll syndrome | autosomal recessive metabolic disorder affecting enzymes involved in bilirubin metabolism |
1 | list | Autosomal recessive spastic ataxia of Charlevoix-Saguenay | autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is a neurodegenerative disorder characterised by early-onset cerebellar ataxia with spasticity, a pyramidal syndrome and peripheral neuropathy |
1 | list | Oikophobia | aversion to home surroundings |
1 | list | Iconophobia | aversion to images, especially religious icons |
1 | list | Eurotophobia | aversion to or dislike of female genitalia |
1 | list | Hexakosioihexekontahexaphobia | aversion to the number 666 or "number of the beast" |
1 | list | Vegaphobia | aversion to vegetarian and vegan people |
1 | list | Hoplophobia | aversion to weapons |
1 | list | Tetraphobia | avoidance of instances of the number 4, due to homophony of the hanzi 四 (4) and 死 (death) in many East Asian languages |
1 | list | Granuloma inguinale | bacterial disease caused by Klebsiella granulomatis (formerly known as Calymmatobacterium granulomatis) characterized by genital ulcers |
1 | list | Bacterial cold water disease | bacterial disease of salmonid fish |
1 | list | Listeriosis | bacterial infection |
1 | list | Paratyphoid fever | bacterial infection caused by one of the three types of Salmonella enterica |
1 | list | Enteric redmouth disease | bacterial infection of freshwater and marine fish |
1 | list | Cholera | bacterial infection of the small intestine |
1 | list | Haemophilus meningitis | bacterial meningitis that has material basis in Haemophilus influenzae infection |
1 | list | Pitted keratolysis | bacterial skin infection of the foot |
1 | list | Fear | basic emotion induced by a perceived threat |
1 | list | Internet sex addiction | behavioral addiction |
1 | list | Food addiction | behavioral addiction that is characterized by the compulsive consumption of palatable foods despite adverse consequences. |
1 | list | Hypergraphia | behavioral condition characterized by the intense desire to write |
1 | list | Factitious disorder imposed on another | behavioral disorder in which an adult fakes an illness in (mostly) a child or other proxy(s) |
1 | list | Diogenes syndrome | behavioral disorder notably characterized by extreme self-neglect and compulsive hoarding |
1 | list | Fixed fantasy | belief or system of beliefs held by a single individual to be genuine, but that cannot be verified in reality |
1 | list | Ideas of reference and delusions of reference | belief that certain gestures, environmental cues, innocuous events, comments and so forth are directed at oneself |
1 | list | Chronic Lyme disease | belief that symptoms are caused by an unproven infection |
1 | list | Alvinolagnia | belly or midriff fetish |
1 | list | Noble rot | beneficial form of a grey fungus, Botrytis cinerea, affecting wine grapes |
1 | list | Osteoid osteoma | benign bone tumor that arises from osteoblasts and was originally thought to be a smaller version of an osteoblastoma |
1 | list | Fissured tongue | benign condition characterized by deep grooves (fissures) in the dorsum of the tongue |
1 | list | Angiokeratoma | benign cutaneous lesion of capillaries, resulting in small marks of red to blue color and characterized by hyperkeratosis |
1 | list | Rhabdomyoma | benign mesenchymal tumor arising from skeletal or cardiac muscle |
1 | list | Cementoblastoma | benign neoplasm of the cementum of the teeth |
1 | list | Pseudolymphoma | benign nepolasm that resembles a malignant lymphoma |
1 | list | Morton's neuroma | benign neuroma of an intermetatarsal plantar nerve, most commonly of the second and third intermetatarsal spaces, which results in the entrapment of the affected nerve; the main symptoms are pain and/or numbness |
1 | list | Splenic tumor | benign or malignant neoplasm that affects the spleen |
1 | list | Dermatofibroma | benign skin growths |
1 | list | Histiocytoma (dog) | benign tumor in dogs; an abnormal growth in the skin of histiocytes |
1 | list | Baritosis | benign type of pneumoconiosis, which is caused by long-term exposure to barium dus |
1 | list | Angiomatosis | benign vascular malformation involving skin, subcutaneous tissue, skeletal muscle and occasionally bone |
1 | list | Ovarian tumor | benign, borderline, or malignant neoplasm involving the ovary |
1 | list | Mongolian spot | benign, flat, congenital birthmark, prevalent among East, South, Southeast, North and Central Asian peoples, Indigenous Oceanians, and Amerindians |
1 | list | Fibrous tissue neoplasm | benign, intermediate, or malignant mesenchymal neoplasm characterized by the presence of neoplastic fibroblasts |
1 | list | Penicillin drug reaction | beta-lactam allergy triggered by penicillin |
1 | list | Cholangiocarcinoma | bile duct adenocarcinoma that has material basis in bile duct epithelial cells. |
1 | list | Ascending cholangitis | bile duct disease that is an inflammation of the bile duct |
1 | list | Caroli disease | bile duct disease that is characterized by abnormal dilatation of the intrahepatic bile ducts |
1 | list | Gallbladder cancer | biliary tract cancer that is located in the gallbladder |
1 | list | Crigler–Najjar syndrome | bilirubin metabolic disorder that involves a build up of bilirubin as bilirubin is not being broken down as a result of a lack or deficiency of the enzyme uridine diphosphate glycosyltransferase (UGT) |
1 | list | Bipolar II disorder | bipolar disorder that is characterized by at least one hypomanic episode and at least one major depressive episode; with this disorder, depressive episodes are more frequent and more intense than manic episodes |
1 | list | Bipolar I disorder | bipolar disorder that is characterized by at least one manic or mixed episode |
1 | list | Avian malaria | birds disease |
1 | list | Preterm birth | birth at less than a specified gestational age |
1 | list | Amelia (birth defect) | birth defect |
1 | list | Gastroschisis | birth defect in which the baby's intestines extend outside of the body through a hole next to the belly button. |
1 | list | Apitoxin | bitter colorless liquid containing proteins, which may produce local inflammation. It may have similarities to sea nettle toxin |
1 | list | Cloacal exstrophy | bladder exstrophy-epispadias-cloacal exstrophy complex that is characterized by a defect in the urethra, bladder and bowel |
1 | list | Hemarthrosis | bleeding into joint spaces |
1 | list | Subarachnoid hemorrhage | bleeding into the subarachnoid space |
1 | list | Subconjunctival bleeding | bleeding underneath the conjunctiva |
1 | list | Pimple | blister containing purulent fluid |
1 | list | Airway obstruction | blockage in the respiratory system |
1 | list | Pulmonary embolism | blockage of the main artery of the lung or one of its branches by a substance that has travelled from elsewhere in the body |
1 | list | Venous thrombosis | blood clot (thrombus) that forms within a vein |
1 | list | Anisopoikilocytosis | blood disorder often caused by some type of anemia |
1 | list | Thrombocythemia | blood platelet disease that is characterized by the presence of high platelet counts in the blood |
1 | list | Angiogenesis | blood vessel formation when new vessels emerge from existing vessels |
1 | list | Von Willebrand disease | blood-clotting disorder |
1 | list | Leukoedema | blue, grey or white appearance of mucosae, particularly the buccal mucosa |
1 | list | Occupational injury | bodily damage resulting from working |
1 | list | Osteofibrous dysplasia | bone benign neoplasm that is located in the mouth and results in an overgrowth of gingival tissue due to irritation or trauma |
1 | list | Ewing's sarcoma | bone cancer that has material basis in neural crest cells derives from undeveloped, undifferentiated neuroectoderm |
1 | list | Adamantinoma | bone cancer that is located in almost exclusively in the long bones |
1 | list | Osteosarcoma | bone cancer that is located in bone that has material basis in cells of mesenchymal origin |
1 | list | Avascular necrosis | bone death caused when the bone no longer receives blood supply |
1 | list | Spinal stenosis | bone deterioration disease that has material basis in bony spurs, disc degeneration, or thickened ligaments which results in narrowing located in spinal cord |
1 | list | Degenerative disc disease | bone deterioration disease that has material basis in gradual dehydration and tears located in intervertebral disc |
1 | list | Clubfoot | bone development disease |
1 | list | Brachydactyly | bone development disease characterized by short fingers and toes |
1 | list | Osteochondrodysplasia | bone development disease that results in defective development of cartilage or bone |
1 | list | Dysostosis | bone development disease that results in defective ossification of located in bone |
1 | list | Osteopenia | bone disease |
1 | list | Skeletal fluorosis | bone disease caused by excessive accumulation of fluoride in the bones |
1 | list | Paget's disease of bone | bone formation disease that has material basis in hyperactive osteoclast which results in abnormal osteoblast bone formation located in skull, located in pelvis, located in vertebral column, located in set of limbs |
1 | list | Smith's fracture | bone fracture |
1 | list | Osteomyelitis | bone inflammation disease that has material basis in infection located in bone or located in bone marrow |
1 | list | Golfer's elbow | bone inflammation disease that results in inflammation located in epicondyle |
1 | list | Spaceflight osteopenia | bone loss caused by microgravity |
1 | list | Osteomalacia | bone remodeling disease that has material basis in a vitamin D deficiency which results in softening located in bone |
1 | list | Osteosclerosis | bone remodeling disease that results in abnormal elevated bone density or mass |
1 | list | Hyperostosis | bone remodeling disease that results in an abnormal growth of located in bone |
1 | list | Fibrous dysplasia of bone | bone remodeling disease that results in the destruction of normal bone and replacing it with fibrous bone tissue |
1 | list | Osteoporosis | bone resorption disease characterized by decreased density of normally mineralized bone which results in the thinning of bone tissue and decreased mechanical strength |
1 | list | Osteitis fibrosa cystica | bone resorption disease that has material basis in hyperparathyroidism which results in hyperactivity in osteoclasts, deformity, and loss of mass located in bone |
1 | list | Spondylolisthesis | bone structure disease that has material basis in displacement located in set of vertebrae |
1 | list | Spondylolysis | bone structure disease that involves a defect located in lumbar vertebral column. |
1 | list | Torus palatinus | bony protrusion on the palate |
1 | list | Heterotopic pregnancy | both extra-uterine (ectopic pregnancy) and intrauterine pregnancy occur simultaneously |
1 | list | Bovine spongiform encephalopathy | bovine counterpart to variant Creutzfeldt-Jakob disease |
1 | list | Constipation | bowel dysfunction that is characterized by infrequent or difficult evacuation of feces. |
1 | list | Brachial plexus injury | brachial plexus neuropathy characterized by an abnormality, usually caused by disease or trauma, located in the brachial plexus |
1 | list | Atypical teratoid rhabdoid tumor | brain cancer that is usually located in the brain, but can occur anywhere in the central nervous system |
1 | list | Akinetic mutism | brain disease characterized by marked reduction of nearly all motor functions including facial expressions, gestures and speech output, but with some degree of alertness |
1 | list | Migraine | brain disease characterized by recurrent headaches on one side |
1 | list | Encephalitis | brain disease that is characterized as an acute inflammation of the brain with flu-like symptoms |
1 | list | Basal ganglia disease | brain disease that is characterized by dysfunction of the basal ganglia which help start and control movement |
1 | list | Hepatic encephalopathy | brain disease that is characterized by loss of brain function, the occurrence of confusion, altered level of consciousness, and coma that results when the liver is unable to remove toxins from the blood |
1 | list | Mild cognitive impairment | brain function syndrome |
1 | list | Diffuse intrinsic pontine glioma | brainstem tumor |
1 | list | Rib fracture | break in a rib bone |
1 | list | Skull fracture | break in one or more of the eight bones that form the cranial portion of the skull |
1 | list | Basilar skull fracture | break of a bone in the base of the skull |
1 | list | Humerus fracture | break of the humerus bone in the upper arm |
1 | list | Proximal humerus fracture | break of the upper part of the bone of the arm |
1 | list | Mandibular fracture | break through the mandibular bone |
1 | list | Fibroadenoma | breast benign neoplasm comprised of fibrous and glandoular tissues located in breast |
1 | list | Emotional and behavioral disorders | broad class of mental disorder |
1 | list | Dyssomnia | broad classification of sleeping disorders involving difficulty getting to sleep, remain sleeping, or of excessive sleepiness |
1 | list | Alcoholism | broad term for problems with alcohol |
1 | list | Chronic leukemia | broad type of leukemia; disjoint with acute leukemia |
1 | list | Aspiration pneumonia | bronchopneumonia that develops due to the entrance of foreign materials into the lungs usually oral or gastric contents |
1 | list | Hickey | bruise-like mark caused by the kissing or sucking of the skin |
1 | list | Aneurysm | bulge in the wall of a blood vessel |
1 | list | Cicatricial pemphigoid | bullous skin disease characterized by skin lesions and scaring and located in mucous membranes and located in skin |
1 | list | Achilles bursitis | bursitis (inflammation of synovial sac) of bursa situated above the insertion of tendon to calcaneus |
1 | list | Neutropenic enterocolitis | caecitis |
1 | list | Caffeinism | caffeine overdose |
1 | list | Porcelain gallbladder | calcification of the gallbladder believed to be brought on by excessive gallstones |
1 | list | Normophosphatemic familial tumoral calcinosis | calcinosis that is characterized by massive periarticular, and seldom visceral, deposition of calcified tumors |
1 | list | Diffuse idiopathic skeletal hyperostosis | calcinosis that is the calcification or a bony hardening of ligaments in areas where they attach to your spine |
1 | list | Calcinosis | calcium metabolism disease that is the result of the formation of calcium deposits in any soft tissue |
1 | list | Rhinolith | calculus present in the nasal cavity |
1 | list | Prayer bump | callus on the forehead of some Muslims |
1 | list | Cervical cancer | cancer arising from the cervix, caused by a sexually transmitted virus |
1 | list | Occupational cancer | cancer caused by occupational hazard |
1 | list | Lung cancer | cancer in the lung |
1 | list | Non-Hodgkin lymphoma | cancer of lymph in humans |
1 | list | Colorectal cancer | cancer of the colon or rectum |
1 | list | Ureteral neoplasm | cancer or tumors of the ureter |
1 | list | Cancer in cats | cancer that afflicts cats |
1 | list | Cancer in dogs | cancer that afflicts dogs |
1 | list | Breast cancer | cancer that originates in the mammary gland |
1 | list | Devil facial tumour disease | cancer type affecting Tasmanian devils |
1 | list | Esophageal candidiasis | candidiasis that involves fungal infection of the esophagus by Candida albicans in immunocompromised people, resulting in lesions, bleeding, painful swallowing and substernal pain |
1 | list | Oral candidiasis | candidiasis that involves fungal infection of the mucous membrane of the mouth by Candida species, which is characterized by thick white or cream-colored deposits on inflamed mucosal membranes |
1 | list | Pyruvate dehydrogenase deficiency | carbohydrate metabolic disorder characterized by the buildup of lactic acid in the body and a variety of neurological problems and caused by a deficiency of one of the three enzymes in the pyruvate dehydrogenase complex |
1 | list | Fructose bisphosphatase deficiency | carbohydrate metabolic disorder that has material basis in a deficiency of fructose-1,6-bisphosphatase resulting in hypoglycemia and metabolic acidosis on fasting due to insufficient fructose bisphosphatase for gluconeogenesis |
1 | list | Galactosemia | carbohydrate metabolic disorder that involves a defect in galactose metabolism resulting in toxic levels of galactose 1-phosphate in various tissues |
1 | list | Congenital disorder of glycosylation | carbohydrate metabolic disorder that involves deficient or defective glycosylation of a variety of tissue proteins and/or lipids |
1 | list | Nesidioblastosis | carbohydrate metabolic disorder that involves low blood glucose resulting from an excess of insulin |
1 | list | Glucose-6-phosphate dehydrogenase deficiency | carbohydrate metabolic disorder that is characterised by abnormally low levels of glucose-6-phosphate dehydrogenase (abbreviated G6PD or G6PDH) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Clear cell carcinoma | carcinoma (i.e. not a sarcoma) showing clear cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Squamous cell carcinoma | carcinoma that derives from squamous epithelial cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Transitional cell carcinoma | carcinoma that derives from transitional epithelial cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Adenocarcinoma | carcinoma that has material basis in abnormally proliferating cells, derives from epithelial cells, which originate in glandular tissue |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Acinic cell carcinoma | carcinoma that has material basis in abnormally proliferating cells, derives from spindle cells and/or derives from giant cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lymphoepithelioma-like carcinoma | carcinoma that is a malignant epithelial neoplasm densely infiltrated by lymphoid cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Carcinoma in situ | carcinoma that is an early development defined by the absence of invasion of surrounding tissues |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mucoepidermoid carcinoma | carcinoma that is characterized by squamous cells, mucus-secreting cells, and intermediate cells. It can occur in several anatomic sites, including parotid gland, oral cavity, paranasal sinus, skin, breast, lung, larynx, and lacrimal ducts |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Primary peritoneal carcinoma | carcinoma that is located in the inside of the abdomen |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Embryoma | carcinosarcoma and embryonal cancer that is located in embryonic tissue and results in a mass of rapidly growing cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Adenomyoma | carcinosarcoma that has material basis in gland and muscle components |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pulseless electrical activity | cardiac arrest with electrical signal but insufficient pumping |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Variant angina | cardiac chest pain at rest that occurs in cycles |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Left bundle branch block | cardiac conduction abnormality seen on the electrocardiogram |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Heart cancer | cardiovascular cancer located in the heart |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Congenital heart defect | cardiovascular disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Heart disease | cardiovascular system disease that involves the heart |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Heart block | cardiovascular system disease that involves the heart's electrical conduction system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Vascular disease | cardiovascular system disease that primarily affects the blood vessels |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Operation Aderlass | case of investigation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Odd-eyed cat | cat with one blue eye and one eye either green, yellow, or brown;feline form of complete heterochromia. The condition most commonly affects white-colored cats, but may be found in a cat of any color, provided that it possesses the white spotting gene |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Zonular cataract and nystagmus | cataract that has material basis in mutation in the NHS gene on chromosome Xp22 |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cervical fracture | catastrophic fracture of any of the seven cervical vertebrae in the neck |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Echopraxia | catatonic behaviour, repetitive imitation of the movements of another person |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Somatic symptom disorder | category of mental disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Parasomnia | category of sleep disorders |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Refractive error | cause of vision problems |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Angiomyolipoma | cell type benign neoplasm that from perivascular epithelioid cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ganglioglioma | cell type benign neoplasm that has material basis in glial-type cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ameloblastoma | cell type benign neoplasm that has material basis in odontogenic epithelium |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hemangioma | cell type benign neoplasm that has physical basis in endothelial cells that line blood vessels and is characterised by increased number of normal or abnormal vessels filled with blood |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Leiomyoma | cell type benign neoplasm that is a benign tumor of smooth muscle cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chondroma | cell type benign neoplasm that is a cartilaginous tumor encapsulated with a lobular growing pattern |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gonadoblastoma | cell type benign neoplasm that is composed of a mixture of gonadal elements |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Adenoma | cell type benign neoplasm that is composed of epithelial tissue in which tumor cells form glands or glandlike structures |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Papilloma | cell type benign neoplasm that is composed of epithelial tissue on papillae of vascularized connective tissue |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sarcoma | cell type cancer that has material basis in abnormally proliferating cells derived from embryonic mesoderm |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Carcinoma | cell type cancer that has material basis_in abnormally proliferating cells derives from epithelial cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Precancerous condition | cellular proliferation that results in abnormal growths in the body, which do not invade or destroy the surrounding tissue, but in time will transform into a cancer |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lentigo maligna | cellular subtype of malignant melanoma, a pigmented lesion composed of melanocytes occurring on sun-exposed skin, usually the face and neck |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Neurodegeneration | central nervous system disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Restless legs syndrome | central nervous system disease characterized by throbbing, pulling creeping or other unpleasant sensations in the legs and the irresistible urge to move them |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Meningoencephalitis | central nervous system disease that involves encephalitis which occurs along with meningitis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Neuroinflammation | central nervous system disease that is characterized by neuron inflammation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Encephalopathy | central nervous system diseases located in the brain |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Locoweed | central nervous system disorder of animals |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Caffeine dependence | central nervous system stimulant drug which occurs in nature as part of the coffee, tea, yerba mate and other plants |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cerebellar ataxia | cerebellar disease characterized by ataxia originating in the cerebellum. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Leukodystrophy | cerebral degeneration characterized by dysfunction of the white matter of the brain |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Alpers' disease | cerebral degeneration that results in progressive degeneration of grey matter in the cerebrum and has symptom convulsions |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Choroid plexus tumor | cerebral ventricle cancer that is located in the plexus located in the ventricles of the brain |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Intracranial aneurysm | cerebrovascular disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Vietnamese tuberculosis | certain forms of chronic melioidosis that look clinically very similar to tuberculosis; named after the clinical appearance of the disease in American soldiers returning from the Vietnam War |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cervical polyp | cervix disease characterized by a benign polyp on the surface of the cervical canal |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cervical weakness | cervix disease that is characterized by the beginning of dilation and effacement of a pregnant woman's cervix before her pregnancy has reached term |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Barakat syndrome | characterized by autosomal dominant inheritance of hypoparathyroidism, sensorineural deafness and progressive renal failure that has material basis in chromosome deletion that results in haploinsufficiency of the GATA3 gene on chromosome 10p14 |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Angular cheilitis | cheilitis characterized by inflammation of one or both of the corners of the mouth |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mendelson's syndrome | chemical pneumonitis or aspiration pneumonitis caused by aspiration during anaesthesia, especially during pregnancy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chemotherapy-induced acral erythema | chemotherapy-induced dermal side effects tassociated with the use of cytostatic agents |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Angina | chest discomfort due to not enough blood flow to heart muscle |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pulmonary laceration | chest injury in which lung tissue is torn or cut |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lymphoid leucosis | chicken disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Malignant rhabdoid tumour | childhood kidney neoplasm that is located in the in the kidney as well as other locations outside the kidneys such as the liver, muscle, heart, lung, soft tissues, skin, the central nervous system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lennox–Gastaut syndrome | childhood-onset epilepsy with triad of signs including frequent seizures of multiple types, an abnormal EEG pattern of less than 2.5 Hz slow spike wave activity, and moderate to severe intellectual impairment |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Childhood schizophrenia | childhood-onset mental disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Spoiled child | children who exhibit behavioral problems from being overindulged by their parents |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chilblains | chillblains |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Vertebral subluxation | chiropractic concept |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cholecystitis | cholangitis that is characterized by an inflammation that is located in the gallbladder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Choroid plexus carcinoma | choroid plexus cancer that has material basis in epithelial cells of the choroid plexus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Down syndrome | chromosomal condition characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Polyploidy | chromosomal constitution of a cell containing multiples of the normal number of chromosomes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Wolf–Hirschhorn syndrome | chromosome abnormality with a distinct craniofacial phenotype and intellectual disability |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Diploid triploid mosaic | chromosome disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ring chromosome | chromosome whose arms fused into a ring |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Occupational disease | chronic ailment that occurs as a result of work or occupational activity; aspect of occupational safety and health |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dermatitis herpetiformis | chronic blistering skin condition, characterised by blisters filled with a watery fluid |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pemphigus vulgaris | chronic blistering skin disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Fox–Fordyce disease | chronic blockage of the sweat gland ducts with a secondary, non-bacterial inflammatory response to the secretions and cellular debris in the cysts |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Banti's syndrome | chronic congestive enlargement of the spleen[2] resulting in premature destruction of the red blood cells by the spleen. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Allergic conjunctivitis | chronic conjunctivitis that is an inflammation of the conjunctiva involing red, itchy, and watery eyes a resulting from an exposure to an allergen or an irritant |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Fibromyalgia | chronic disorder of unknown etiology characterized by pain, stiffness, and tenderness |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Eumycetoma | chronic granulomatous[1] fungal disease[2] of humans, affecting mainly the limbs, and sometimes the abdominal and chest walls or the head |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Interstitial cystitis | chronic inflammatory condition of the submucosal and muscular layers of the bladder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chronic periodontitis | chronic inflammatory process that affects the tissues that surround and support the teeth |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Morsicatio buccarum | chronic irritation or injury of inner mouth-lining caused by repetitive chewing, biting |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ringbone | chronic joint disease of hoofed animals |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chronic myelomonocytic leukemia | chronic leukemia characterized by monocytosis, increased monocytes in the bone marrow, variable degrees of dysplasia, but an absence of immature granulocytes in the blood |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chronic neutrophilic leukemia | chronic leukemia characterized by neutrophilic leukocytosis with no detectable Philadelphia chromosome or BCR/ABL fusion gene |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Large granular lymphocytic leukemia | chronic lymphocytic leukemia that exhibits an unexplained, chronic (> 6 months) elevation in large granular lymphocytes (LGLs) in the peripheral blood |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hairy cell leukemia | chronic lymphocytic leukemia that is characterized by over production of B cells (lymphocytes) by the bone marrow where the B cells appear hairy under a microscope |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Delayed sleep phase disorder | chronic mismatch between a person's normal daily rhythm, compared to other people and societal norms |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Post-vasectomy pain syndrome | chronic pain condition |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Epidermolysis bullosa acquisita | chronic subepidermal blistering disease associated with autoimmunity to type VII collagen |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Blepharophyma | chronic swelling of eyelids |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tendinosis | chronic tendon injury with damage to a tendon at a cellular level |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pressure ulcer | chronic ulcer of skin where the ulcer is an ulceration of tissue deprived of adequate blood supply by prolonged pressure |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Physical dependence | chronic use of a tolerance forming drug, in which abrupt or gradual drug withdrawal causes unpleasant physical symptoms |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Kashin–Beck disease | chronic, endemic osteochondropathy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Idiopathic pulmonary fibrosis | chronic, irreversible and ultimately fatal disease characterized by a progressive decline in lung function |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bardet–Biedl syndrome | ciliopathic human genetic disorder that produces many effects and affects many body systems |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Irregular sleep–wake rhythm | circadian sleep disorder characterized by at least three sleep episodes per 24-hour period, irregularly from day to day |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Health effects of tobacco | circumstances, mechanisms, and factors of tobacco consumption on human health |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Weather pains | claims of pain associated with changes in barometric pressure, humidity or other weather phenomena |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Inborn errors of metabolism | class of disease including endocrine diseases, nutritional diseases and metabolic diseases |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cardiovascular disease | class of diseases that involve the heart or blood vessels |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Skin condition | class of disorder that affects skin, hair or nails |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sphingolipidoses | class of lipid storage disorders relating to sphingolipid metabolism |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Environmental disease | class of non-hereditary diseases |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mange | class of skin diseases caused by parasitic mites |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Skin cancer | class of skin illnesses, tumor or cancer of the skin |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Movement disorders | clinical syndromes with either an excess of movement or a paucity of voluntary and involuntary movements |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Comedo | clogged hair follicle in the skin |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cyst | closed sac growth on the body |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Portal vein thrombosis | clotting within the hepatic portal vein |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cataract | clouding of the lens inside the eye, which leads to low vision |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Benzodiazepine withdrawal syndrome | cluster of symptoms that emerge when a person who has taken benzodiazepines and has developed a physical dependence undergoes dosage reduction or discontinuation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Metabolic syndrome | clustering of medical conditions (giving a total of 16 possible combinations giving the syndrome) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Freckle | clusters of concentrated melanin |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Isosporiasis | coccidiosis that involves infection of the epithelial cells of the small intestine with Cystoisospora belli, which results in nonbloody diarrhea with crampy abdominal pain, malabsorption and weight loss |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Amnesia | cognitive disorder where the memory is disturbed or lost and involves the loss of memories previously established, loss of the ability to create new memories, continuous high blood pressure and severe shock may also caused amnesia |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Anxiety disorder | cognitive disorder with an excessive, irrational dread of everyday situations |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Diversion colitis | colitis caused by diversion of the fecal stream due to complication of ileostomy or colostomy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ischemic colitis | colitis caused by inadequate blood supply to the colon |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chemical colitis | colitis caused by introduction of various chemicals |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Collagenous colitis | colitis characterized by a distinctive thickening of the subepithelial collagen table |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lymphocytic colitis | colitis characterized by an accumulation of lymphocytes in the colonic epithelium and connective tissue (lamina propria) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Clostridioides difficile infection | colitis characterized by an overgrowth of Clostridium difficile bacteria |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Microscopic colitis | colitis that can only be diagnosed by the examination of colon tissue under a microscope |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mixed connective tissue disease | collagen disease that is considered an overlap of three diseases, systemic lupus erythematosus, scleroderma, and polymyositis with very high titers of circulating antinuclear antibody to a ribonucleoprotein antigen |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Atelectasis | collapse or closure of a lung resulting in reduced or absent gas exchange |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Subdural hygroma | collection of cerebrospinal fluid (CSF), without blood, located under the dural membrane |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sarcoglycanopathy | collection of diseases resulting from mutations in any of the four sarcoglycan genes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Liver abscess | collection of pus within the liver as a result of infection by bacteria, protozoa, or other agents |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Megacolon | colonic disease that is characterized by an abnormal dilation of the colon |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Culture-bound syndrome | combination of symptoms that are considered to be a recognizable disease only within a specific culture |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Purine nucleoside phosphorylase deficiency | combined T cell and B cell immunodeficiency that is a rare autosomal recessive metabolic disorder that has material basis in mutation in the PNP gene and characterized mainly by decreased T-cell function |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Severe combined immunodeficiency | combined T cell and B cell immunodeficiency that is caused by a defect in several genes encoding for B and T lymphocytes resulting in individuals with non-functional immune systems |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Wernicke–Korsakoff syndrome | combined presence of Wernicke's encephalopathy (WE) and Korsakoff's syndrome |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Atrial flutter | common abnormal heart rhythm that starts in the atrial chambers of the hear |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lightheadedness | common and typically unpleasant sensation of dizziness |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Nasopharynx cancer | common cancer originating in the nasopharynx |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Amalgam tattoo | common discoloration of tissue in the mouth |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Fear of the dark | common fear or phobia among children and, to a varying degree, adults |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Frontal lobe epilepsy | common form of epilepsy that may appear to be related to a psychiatric problem or a sleep disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ear mite | common name |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Canker | common name for a tree pathogen |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Surfer's ear | common name for an abnormal bone growth within the external ear canal |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Facial nerve paralysis | common problem that involves the paralysis of any structures innervated by the facial nerve |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Livedo reticularis | common skin finding consisting of a mottled reticulated vascular pattern that appears as a lace-like purplish discoloration of the skin |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pinguecula | common type of conjunctival degeneration in the eye |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Common cold | common viral infection of upper respiratory tract |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Infectious mononucleosis | common viral infectious disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Speech disorder | communication disorder that involves difficulty with the act of speech production. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Agnosia | communication disorder that is a loss of ability to recognize objects, persons, sounds, shapes, or smells while the specific sense is not defective nor is there any significant memory loss. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Atypical hemolytic uremic syndrome | complement deficiency that is characterized by mechanical hemolytic anemia, thrombocytopenia, and renal dysfunction |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Brain death | complete and irreversible loss of brain function |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Acquired generalized lipodystrophy | complete generalized lipodystrophy that is charcterized by generalized disappearance of fat occurring during childhood and adolescence where normal body fat is present at birth |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Invasive hydatidiform mole | complete hydatidiform mole or very rarely a partial mole that invades the myometrium |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Aspermia | complete lack of semen with ejaculation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Blindness | complete or nearly complete vision loss |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Impossible syndrome | complex combination of human congenital malformations (birth defects) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Epilepsy syndromes | complex of signs and symptoms that define a unique epileptic condition |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Immune reconstitution inflammatory syndrome | complication of anti-HIV treatment |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mirizzi's syndrome | complication of cholelithiasis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Twin-to-twin transfusion syndrome | complication of disproportionate blood supply, resulting in high morbidity and mortality |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Twin reversed arterial perfusion | complication of monochorionic twin pregnancies |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gradenigo's syndrome | complication of otitis media and mastoiditis involving the apex of the petrous temporal bone |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Macrophage activation syndrome | complication of several chronic rheumatic diseases of childhood |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Testicular rupture | complication of testicular trauma |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tarsal tunnel syndrome | compression neuropathy and painful foot condition in which the tibial nerve is compressed as it travels through the tarsal tunnel |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Amylophagia | compulsion to consume purified starch (such as cornstarch) in excess |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Low frustration tolerance | concept in Rational Emotive Behavioral Therapy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Calculus (medicine) | concretion of material, usually mineral salts, that forms in an organ or duct of the body |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dwarfism | condition affecting a person or animal short in stature, caused by slow or delayed growth |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Decompression sickness | condition arising on depressurisation of the body |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Traumatic brain injury | condition caused by an external force which has traumatically injured the brain |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Toxic shock syndrome | condition caused by bacterial toxins |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tympanosclerosis | condition caused by hyalinization and subsequent calcification of subepithelial connective tissue of TM and middle ear |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Heat illness | condition caused by the failure of the human body to dissipate heat in a hot environment |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Rhinophyma | condition causing development of a large, bulbous nose associated with granulomatous infiltration, commonly due to untreated rosacea |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Saddle nose | condition characterized by a loss of height of the nose, because of the collapse of the bridge |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tinea versicolor | condition characterized by a rash on the trunk and proximal extremities |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Harlequin syndrome | condition characterized by asymmetric sweating and flushing on the upper thoracic region of the chest, neck and face |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gout | condition characterized by painful swelling of the joints, which is caused by deposition of urate crystals |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Vitamin deficiency | condition due to a deficiency of one or more essential vitamins |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Malnutrition in children | condition in children from eating a diet in which some nutrients are either not enough or are too much |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Alabama rot | condition in dogs believed to be caused by toxins produced by bacteria |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Postural orthostatic tachycardia syndrome | condition in which a change from lying to standing causes an abnormally large increase in heart rate |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Motion sickness | condition in which a disagreement exists between visually perceived movement and the vestibular system's sense of movement |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hyperspermia | condition in which a male has an abnormally large ejaculate volume |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Noise-induced hearing loss | condition in which a person loses the ability to hear due to exposure to high intensity sound |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sleep sex | condition in which a person will engage in sexual activities while asleep |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gestational diabetes | condition in which a woman without diabetes develops high blood sugar levels during pregnancy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sexual anhedonia | condition in which an individual cannot feel pleasure from an orgasm |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Transsexual | condition in which an individual identifies with a gender inconsistent or not culturally associated with their biological sex |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Perforated ulcer | condition in which an untreated ulcer can burn through the wall of the stomach (or other areas of the gastrointestinal tract), allowing digestive juices and food to leak into the abdominal cavity |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Macrodontia (tooth) | condition in which any tooth or teeth appear larger than normal |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypothermia | condition in which core temperature drops below the required temperature for normal metabolism and body functions as roger banks said |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Rhabdomyolysis | condition in which damaged skeletal muscle breaks down rapidly |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Alopecia areata | condition in which hair is lost from some or all areas of the body |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Compartment syndrome | condition in which increased pressure within one of the body's compartments results in insufficient blood supply to tissue within that space |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Obsessive love | condition in which one person feels an overwhelming obsessive desire to possess and protect another person toward whom one feels a strong attraction, with an inability to accept failure or rejection |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Splenic infarction | condition in which oxygen supply to the spleen is interrupted |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lactose intolerance | condition in which people have symptoms due to a decreased ability to digest lactose |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Polyradiculoneuropathy | condition in which polyneuropathy and polyradiculopathy occur together |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Coagulopathy | condition in which the blood’s ability to coagulate (form clots) is impaired |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypoxia (medical) | condition in which the body or a region of the body is deprived of adequate oxygen supply at the tissue level |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Heart failure | condition in which the heart is unable to provide sufficient pump action |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Laryngeal paralysis | condition in which the nerves and muscles that control the movements of one or both arytenoid cartilages of the larynx cease to function |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tennis elbow | condition in which the outer part of the elbow becomes sore and tender |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hemoglobinuria | condition in which the oxygen transport protein hemoglobin is found in abnormally high concentrations in the urine |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Thymic hypoplasia | condition in which the thymus is underdeveloped or involuted |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hyperinsulinemia | condition in which there are excess levels of insulin circulating in the blood relative to the level of glucose |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypertelorism | condition in which there is an abnormally increased distance between two organs or bodily parts; most often, this term is referring to an increased distance between the orbits (orbital hypertelorism) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Normal pressure hydrocephalus | condition in which there is excess cerebrospinal fluid in the ventricles, and with normal or slightly elevated cerebrospinal fluid pressure |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Brachymetatarsia | condition in which there is one or more abnormally short or overlapping toes metatarsals |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Nyctalopia | condition making it difficult or impossible to see in relatively low light |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Loxoscelism | condition occasionally produced by the bite of the recluse spiders |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Diverticulosis | condition of having diverticula (outpocketings) in the wall of the intestine |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dry eye syndrome | condition of having dry eyes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Polycephaly | condition of having more than one head |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Nystagmus | condition of involuntary eye movement |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Deafblindness | condition of little or no useful sight and little or no useful hearing |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypertensive emergency | condition of markedly elevated blood pressure with diastolic pressure typically greater than 120 mm Hg |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hyperthymesia | condition of possessing an extremely detailed autobiographical memory |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Reduced affect display | condition of reduced emotional reactivity in an individual |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Venous stasis | condition of slow blood flow in the veins, usually of the legs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dual diagnosis | condition of suffering from a mental illness and a comorbid substance abuse problem |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Far-sightedness | condition of the eye |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Posterior vitreous detachment | condition of the eye in which the vitreous membrane separates from the retina |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Leukoplakia | condition of the mucous membranes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Macular telangiectasia | condition of the retina |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Birth defect | condition present at birth regardless of cause; human disease or disorder developed prior to birth |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Computer vision syndrome | condition resulting from focusing the eyes on a computer or other display device for protracted, uninterrupted periods of time |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Antidepressant discontinuation syndrome | condition that can occur following the interruption, dose reduction, or discontinuation of antidepressant drugs, including selective serotonin re-uptake inhibitors (SSRIs) or serotonin–norepinephrine reuptake inhibitors (SNRIs) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pyoderma gangrenosum | condition that causes tissue to become necrotic, causing deep ulcers that usually occur on the legs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Substance intoxication | condition that follows the administration of a psychoactive drug - a type of substance-related disorders |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Paresis | condition typified by a weakness of voluntary movement |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sialolithiasis | condition where a calcified mass or sialolith forms within a salivary gland, usually in the duct of the submandibular gland |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cardiorenal syndrome | condition where a dysfunction of heart or kidney results in failure of the other organ |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Elevated alkaline phosphatase | condition where alkaline phosphatase exceeds normal levels in the blood |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Neuroglycopenia | condition where both glucemic and sympathetic effects are the cause of signs and symptoms |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Childhood obesity | condition where excess body fat negatively affects a child's health or well-being |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Algaemia | condition where green algae is found in the blood |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Aphantasia | condition where one does not possess a functioning mind's eye and cannot voluntarily visualize imagery |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Levocardia | condition where the heart is in the correct anatomic position but some or all of the other thoracoabdominal viscera are in the opposite lateral orientation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Stenosis of pulmonary artery | condition where the pulmonary artery is subject to an abnormal constriction |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Patent ductus arteriosus | condition wherein the ductus arteriosus fails to close after birth |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pigeon toe | condition which causes the toes to point inward when walking |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Word salad | confused unintelligible jumble of words and phrases |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Multiple abnormalities | congenital abnormalities that affect more than one organ or body structure |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cryptophthalmos | congenital abnormality characterized by the presence of a continuous layer of skin extending over the eyeballs and the absence of eyelids and the palpebral fissure |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Facial cleft | congenital abnormality consisting of an opening or gap in the face, which results from incomplete fusion of one or more of the embryonic facial prominences |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Michel aplasia | congenital abnormality of the inner ear |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Fibular hemimelia | congenital absence of the fibula |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Al-Raqad syndrome | congenital autosomal recessive syndrome discovered by Jordanian physician Mohammad Al-Raqad |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Situs inversus | congenital condition in which the major visceral organs are reversed from their normal positions |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Trigonocephaly | congenital condition of premature fusion of the metopic suture leading to a triangular shaped forehead. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Coarctation of the aorta | congenital condition whereby the aorta is narrow, usually in the area where the ductus arteriosus (ligamentum arteriosum after regression) inserts. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cephalic disorder | congenital conditions that stem from damage to, or abnormal development of, the budding nervous system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Radial aplasia | congenital defect which affects the formation of the radius bone in the arm |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Vaginal anomalies | congenital defect; abnormal or absent vagina |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pectus excavatum | congenital deformity of the chest |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Morning glory disc anomaly | congenital deformity resulting from failure of the optic nerve to completely form in utero |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Microtia | congenital deformity where the pinna (external ear) is underdeveloped |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Vascular malformation | congenital disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Albinism | congenital disorder causing skin to lack pigmentation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Laron syndrome | congenital disorder characterized by marked short stature associated with normal or high serum growth hormone (GH) and low serum insulin-like growth factor-1 (IGF-I) levels which fail to rise after exogenous GH administration |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ectopic kidney | congenital disorder describing a kidney that is not located in its usual position |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Caudal regression syndrome | congenital disorder in humans caused by abnormal fetal development of the lower spine |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Supernumerary body part | congenital disorder involving the growth of an additional part of the body and a deviation from the body plan |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dysmelia | congenital disorder of a limb |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Biliary atresia | congenital disorder of digestive system investigation of choice of the disease is MRCP |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Porencephaly | congenital disorder of nervous system characterized by cysts or cavities within the cerebral hemisphere. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Holoprosencephaly | congenital disorder of the nervous system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Laryngomalacia | congenital disorder of upper respiratory system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Melnick–Needles syndrome | congenital disorder that affects primarily bone development. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Darwin's tubercle | congenital ear condition which often presents as a thickening on the helix at the junction of the upper and middle thirds |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Crisscross heart | congenital heart defect |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tetralogy of Fallot | congenital heart defect that is present at birth. Symptoms include episodes of bluish color to the skin embryology includes the displacement of the inphondibulor septem anterio superiorly |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cor triatriatum | congenital heart defect where the left atrium (cor triatriatum sinistrum) or right atrium (cor triatriatum dextrum) is subdivided by a thin membrane, resulting in three atrial chambers |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypoplastic left heart syndrome | congenital heart disease characterized by abnormal development of the left-sided structures of the heart |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dextro-Transposition of the great arteries | congenital heart disease characterized by complete inversion of the great vessels where the aorta incorrectly arises from the right ventricle and the pulmonary artery incorrectly arises from the left ventricle |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Congenital dyserythropoietic anemia | congenital hemolytic anemia characterized by ineffective erythropoiesis, and resulting from a decrease in the number of red blood cells (RBCs) in the body and a less than normal quantity of hemoglobin in the blood |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hereditary spherocytosis | congenital hemolytic anemia characterized by the production of red blood cells with a sphere shape, rather than the normal biconcave disk shape |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cornea plana 1 | congenital hereditary deformity of the eye surface |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gunther disease | congenital human disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Arthrogryposis | congenital joint contracture in two or more areas of the body |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ectopia cordis | congenital malformation in which the heart is abnormally located either partially or totally outside of the thorax |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Aphallia | congenital malformation in which the phallus (penis or clitoris) is absent |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pachygyria | congenital malformation of the cerebral hemisphere resulting in unusually thick convolutions of the cerebral cortex. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pyruvate kinase deficiency | congenital nonspherocytic hemolytic anemia that has material basis in homozygous or compound heterozygous mutation in the PKLR gene on chromosome 1q22 |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Vascular anomaly | congenital or acquired |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Megaduodenum | congenital or acquired dilation and elongation of the duodenum |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cystic kidney disease | congenital or acquired kidney disorder characterized by the presence of renal cysts |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Harlequin-type ichthyosis | congenital skin disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Nemaline myopathy | congenital structural myopathy characterized by generally non-progressive muscle weakness of varying severity |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Keshan disease | congestive cardiomyopathy caused by a combination of dietary deficiency of selenium and the presence of a mutated strain of Coxsackievirus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pulmonary heart disease | congestive heart failure that involves a failure of the right side of the heart and is characterized by an enlargement of the right ventricle of the heart as a response to increased resistance or high blood pressure in the lungs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Heart failure with preserved ejection fraction | congestive heart failure wherein the amount of blood pumped from the heart's left ventricle with each beat (ejection fraction) is greater than 50% |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Craniopagus twins | conjoined twins who are fused at the cranium |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Conjunctival squamous cell carcinoma | conjunctival cancer characterized by abnormal growth of dysplastic squamous epithelial cells on the surface of the eye that arises from the conjunctiva that has infiltrated beyond the confines of the epithelial basement membrane |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Infantile myofibromatosis | connective tissue benign neoplasm that is characterized by the development of benign tumors in the skin, striated muscles, bones, and in exceptional cases, visceral organs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Kaposi's sarcoma | connective tissue cancer |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chondrosarcoma | connective tissue cancer that has material basis in cells derived from transformed cells that produce cartilage |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Fibrosarcoma | connective tissue cancer that has material basis in fibrous connective tissue and characterized by the presence of immature proliferating fibroblasts or undifferentiated anaplastic spindle cells in a storiform pattern |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ossification of the posterior longitudinal ligament | connective tissue disease characterized by ectopic ossification of the posterior longitudinal spinal ligament resulting in spinal cord compression, myelopathy and hyperreflexia |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Funisitis | connective tissue disease that is an inflammation of the connective tissue of the umbilical cord |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Arterial tortuosity syndrome | connective tissue disease that is characterized by elongation and generalized tortuosity of the major arteries including the aorta |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Synovitis | connective tissue disease that results in inflammation located in synovial membrane that lines a synovial joint which causes pain and swelling |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Malingering | conscious simulation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Subclavian steal syndrome | constellation of signs and symptoms that arise from retrograde (reversed) blood flow in the vertebral artery or the internal thoracic artery, due to a proximal stenosis (narrowing) and/or occlusion of the subclavian artery |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sweating sickness | contagious disease of humans that struck England,and Europe, ca. 1485-1551 |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Low-functioning autism | controversial term applied to people with autism who have an intellectual disability and/or high support needs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Megalocornea | corneal disease characterized by a bilaterally enlarged corneal diameter without an increase in intraocular pressure |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Keratoconus | corneal disease characterized by structural changes within the cornea causing it to thin and change, leading to a protruding conical shape |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sclerocornea | corneal disease in which the cornea blends with sclera, resulting in clouding of the cornea |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Keratitis | corneal disease that is characterized by inflammation of the cornea. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Fuchs' dystrophy | corneal dystrophy characterized by accumulation of focal outgrowths (guttae) and thickening of Descemet's membrane, leading to corneal edema and loss of vision |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Macular corneal dystrophy | corneal dystrophy that is characterized by corneal haze, severe photophobia at night ,gradual vision impairment ,bilateral loss of vision, eventually necessitating corneal transplantation resulting from progressive punctate opacities in the cornea |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Anomalous left coronary artery from the pulmonary artery | coronary artery anomaly in which the left coronary artery (LCA) branches off the pulmonary artery instead of the aortic sinus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hill–Sachs lesion | cortical depression in the posterolateral head of the humerus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cortisone reductase deficiency | cortisone reductase deficiency that has material basis in homozygous or compound heterozygous mutation in the H6PD gene on chromosome 1p36 |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Post-viral cough | cough that follows a viral respiratory tract infection |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Optic neuropathy | cranial nerve disease that is located in the optic nerve |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Meige's syndrome | cranio-facial dystonia that is accompanied by blepharospasm |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Suudu | culture-specific syndrome in South India |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Presbycusis | cumulative effect of aging on hearing |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Evil eye | curse believed to be cast by a malevolent glare, causing many cultures to create measures against it |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chromobacteriosis infection | cutaneous condition caused by chromobacteria |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | PHACES Syndrome | cutaneous condition characterized by multiple congenital abnormalities. ("PHACES"=Posterior fossa malformations–hemangiomas–arterial anomalies–cardiac defects–eye abnormalities–sternal cleft and supraumbilical raphe syndrome) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Weber–Christian disease | cutaneous condition characterized by recurrent subcutaneous nodules that heal with depression of the overlying skin |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pilar sheath acanthoma | cutaneous condition most often found on the face, particularly above the upper lip in adults |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Generalized vaccinia | cutaneous condition that occurs 6–9 days after vaccination, characterized by a generalized eruption of skin lesions, and caused by the vaccinia virus. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dermatomycosis | cutaneous mycosis that results in fungal infection located in skin or of its appendages, has material basis in Ascomycota fungi other than the dermatophytes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bartholin's cyst | cyst in a blocked Bartholin's gland |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Odontogenic cyst | cyst in the jaw that arises from tissues of tooth development |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Serous cystadenocarcinoma | cystadenocarcinoma that derives from epithelial cells originating in glandular tissue forming serous lesions |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mucinous cystadenocarcinoma | cystadenocarcinoma that derives from epithelial cells originating in glandular tissue, with a capsulated structure and mucus-producing cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ureterocele | cystic dilatation of the end of a ureter as it enters into the urinary bladder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Neurocysticercosis | cysticercosis of the brain |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Nerve injury | damage to a nerve |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dental barotrauma | damage to a tooth caused by a change of ambient pressure |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Radiation burn | damage to the skin or other biological tissue caused by exposure to radiation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tracheobronchial injury | damage to the tracheobronchial tree |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hyperpigmentation | darkening of an area of skin or nails caused by increased melanin |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Carbon monoxide poisoning | death due to exposure to carbon monoxide |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Taravana | decompression sickness after breath-hold diving |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Anemia | decrease in number of red blood cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Leukopenia | decrease in the number of white blood cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Visual impairment | decreased ability to see |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hemianopsia | decreased vision or blindness (anopsia) in half the visual field, usually on one side of the vertical midline. The most common causes of this damage are stroke, brain tumor, and trauma, and stop the fight ref. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Boil | deep folliculitis, infection of the hair follicle |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bundle branch block | defect of the bundle branches or fascicles in the electrical conduction system of the heart |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Diaphragmatic hernia | defect or hole in the diaphragm that allows the abdominal contents to move into the chest cavity |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Aplasia | defective development or congenital absence of an organ or tissue |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cryptorchidism | defective mammal development |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ectrodactyly | deficiency or absence of one or more central digits of the hand or foot |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Allomnesia | deformation of actual memories |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Boutonniere deformity | deformed position of the fingers or toes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bunion | deformity characterized by lateral deviation of the great toe |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Genu recurvatum | deformity in the knee joint |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hammer toe | deformity of the proximal joint of the second, third or fourth toe |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Macular degeneration | degeneration of macula and posterior pole that is characterized by a loss of vision in the center of the visual field (the macula) resulting from damage to the retina and resulting in blurring of the sharp central vision |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Eburnation | degenerative bone condition |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Variant Creutzfeldt–Jakob disease | degenerative brain disease caused by prions |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Creutzfeldt–Jakob disease | degenerative neurological disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Keratoglobus | degenerative non-inflammatory disorder of the eye in which structural changes within the cornea cause it to become extremely thin and change to a more globular shape than its normal gradual curve |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Spondylosis | degenerative osteoarthritis of the joints between the center of the spinal vertebrae and/or neural foramina |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ramsay Hunt syndrome type 1 | degenerative, neurological disorder characterized by myoclonus epilepsy, intention tremor, progressive ataxia and occasionally cognitive impairment |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Religious delusion | delusion involving religious themes or subject matter |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Reduplicative paramnesia | delusional belief |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Thought withdrawal | delusional belief that thoughts have been 'taken out' of the patient's mind |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Vascular dementia | dementia that involves impairments in cognitive function caused by problems in blood vessels that feed the brain |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Balo concentric sclerosis | demyelinating disease characterized by the fact that the demyelinated tissues form concentric layers |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Central pontine myelinolysis | demyelination disease that is characterized by severe damage to the myelin sheath of the pons' nerve cells and has symptom acute paralysis, has symptom dysphagia, and has symptom dysarthria |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Follicular dendritic cell sarcoma | dendritic cell sarcoma cancer that effects the follicular dendritic cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Amelogenesis imperfecta | dental enamel hypoplasia characterized by abnormal enamel formation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lameness (equine) | departure from the normal gait in animals |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Siderosis | deposition of excess iron in body tissue |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Xanthoma | deposition of yellowish cholesterol-rich material that can appear anywhere in the body in various disease states |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Floater | deposits of various size, shape, consistency, refractive index, and motility within the eye's vitreous humour, which is normally transparent |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Premenstrual dysphoric disorder | depressive disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Post-schizophrenic depression | depressive episode, arising in the aftermath of a schizophrenic psychosis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Acrodermatitis | dermatitis that selectively affects the hands and feet |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chrysiasis | dermatological condition induced by the parenteral administration of gold salts |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lobomycosis | dermatomycosis that results in infection located in skin or located in subcutaneous tissue, has material basis in Lacazia loboi and has symptom crusty plaques, has symptom tumors and results in formation of nodular lesions |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tinea manuum | dermatophytosis that results in fungal skin infection located in hand, has material basis in Ascomycota fungi that belong to a group called dermatophytes and has symptom itching, has symptom burning, has symptom cracking, and has symptom scaling |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gestational pemphigoid | dermatosis of pregnancy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Infantile neuroaxonal dystrophy | describes several similar diseases |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cataphylaxis | deterioration of the natural defense system of the body due to an infection |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Spontaneous bacterial peritonitis | development of a bacterial infection in the peritoneum, despite the absence of an obvious source for the infection |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Heterotopic ossification | development of bony substance in normally soft structures |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Heparin-induced thrombocytopenia | development of thrombocytopenia (a low platelet count), due to the administration of various forms of heparin, an anticoagulant |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | 3C syndrome | developmental malformation syndrome characterized by craniofacial abnormalities, congenital heart defects, and cerebellar brain malformations. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gait abnormality | deviation from normal walking (gait) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Adrenal fatigue | diagnosis of adrenal gland exhaustion |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Atypical small acinar proliferation | diagnosis on prostate biopsy that carries an increased risk of finding prostate cancer on re-biopsy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Conversion disorder | diagnostic category used in some psychiatric classification systems |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Congenital diaphragmatic hernia | diaphragm disease characterized by the lack of development of all or part of the diaphragm, which results in an abnormal opening that allows the stomach and intestines to move into the chest cavity and crowd the heart and lungs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Emotional dysregulation | difficulty controlling and moderating one's emotional reactions |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sexual dysfunction | difficulty experienced by humans during any stage of normal sexual activity |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Rhotacism (speech impediment) | difficulty in pronouncing rhotic ("r") sounds |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lambdacism | difficulty pronouncing "l" sounds |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Executive dysfunction | difficulty with executive functions such as organization, planning ahead, and self-monitoring |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Primary mediastinal B-cell lymphoma | diffuse large B-cell lymphoma that is is characterized by a diffuse proliferation of medium to large B-cells associated with sclerosis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Diverticulitis | digestive disease caused by an inflammation of a herniating pouch (diverticulum) within the wall of the intestine, most often colon |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hernia | digestive system disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Annuloaortic ectasia | dilation of the proximal ascending aorta and aortic annulus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Female infertility | diminished or absent ability of a female to achieve conception |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mind-blindness | disability to be aware of mental states |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Rinderpest | disease (caused by the virus in Q2153407) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chytridiomycosis | disease affecting amphibians |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cytochrome P450 oxidoreductase deficiency | disease and inborn error of metabolism caused by deficiency of cytochrome P450 oxidoreductase (POR) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Nipah virus infection | disease caused by Nipah virus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Nutritional muscular dystrophy | disease caused by a deficiency of selenium and vitamin E in dietary intake |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Milk fever | disease caused by hypocalcemia in pregnant or lactating cows and ewes; can be fatal |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Infectious disease | disease caused by infection of pathogenic biological agents in a host organism |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tick-borne disease | disease caused by infectious agents transmitted by tick bites |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Indium lung | disease caused by inhalation of indium |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Capillariasis | disease caused by nematodes of the genus Capillaria |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Leishmaniasis | disease caused by parasites of the Leishmania type |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Waterborne diseases | disease caused by pathogenic microorganisms that most commonly are transmitted in contaminated fresh water |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gastroesophageal reflux disease | disease caused by stomach acid coming up from the stomach into the esophagus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pediculosis pubis | disease caused by the pubic louse, Pthirus pubis, a parasitic insect notorious for infesting human pubic hair |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gastroenterocolitis | disease characterized by inflammation of the stomach, small intestines, and colon |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gas gangrene | disease for all sorts of living things |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Apple scab | disease in apple trees |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pacheco's disease | disease in parrots |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Valvular heart disease | disease in the valves of the heart |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypertrophic cardiomyopathy | disease in which a portion of the myocardium (heart muscle) is hypertrophic (enlarged) without any obvious cause, creating functional impairment of the heart. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Eosinophilic pneumonia | disease in which an eosinophil, a type of white blood cell, accumulates in the lung |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Alcoholic cardiomyopathy | disease in which the chronic long-term abuse of alcohol (i.e., ethanol) leads to heart failure |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Myopathy | disease in which the muscle fibers do not function, resulting in muscular weakness |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cavitary pneumonia | disease in which the normal lung architecture is replaced by a cavity |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tooth decay | disease involving breakdown of teeth |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Langerhans cell histiocytosis | disease involving clonal proliferation of Langerhans cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Articular cartilage damage | disease involving the articular cartilage of joint |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tooth pathology | disease involving the calcareous tooth |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gastrointestinal disease | disease involving the gastrointestinal tract |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Glomerulopathy | disease involving the renal glomerulus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tongue disease | disease involving the tongue |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Spinal disease | disease involving the vertebral column |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Arthropathy | disease of a joint |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Reproductive system disease | disease of anatomical entity that is located in reproductive system organs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Neurological disorder | disease of anatomical entity that is located in the central nervous system or located in the peripheral nervous system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Musculoskeletal disorder | disease of anatomical entity that occurs in the muscular and/or skeletal system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Anemia in pregnancy | disease of anemia during pregnancy in humans |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Embolism | disease of arteries, arterioles and capillaries |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Intestinal cancer in cats and dogs | disease of cats and dogs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sweating sickness (cattle) | disease of cattle |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Benign tumor | disease of cellular proliferation that results in abnormal growths in the body which lack the ability to metastasize |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Strangles | disease of horses |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dissociative disorder | disease of mental health in which the normally well-integrated functions of memory, identity, perception, or consciousness are separated (dissociated) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cognitive disorder | disease of mental health that affects cognitive functions including memory processing, perception and problem solving |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Impulse control disorder | disease of mental health that involves a failure to resist an impulsive act or behaviour that may be harmful to self or others |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sleep disorder | disease of mental health that involves disruption of sleep patterns |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Developmental disorder | disease of mental health that occur during a child's developmental period between birth and age 18 resulting in retarding of the child's psychological or physical development |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Factitious disorder | disease of mental health where symptoms are deliberately produced, feigned or exaggerated in order to falsely demonstrate the presence of an illness |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Aleutian disease | disease of mustelids caused by a highly contagious parvovirus (carnivore amdoparvovirus 1) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Porcine circovirus associated disease | disease of pig |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Infectious coryza in chickens | disease of poultry |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Paroxysmal nocturnal hemoglobinuria | disease of the blood characterized by destruction of red blood cells by the complement system, a part of the body's innate immune system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Angiopathy | disease of the blood vessels |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | First-degree atrioventricular block | disease of the electrical conduction system of the heart in which the PR interval is lengthened beyond 0.20 seconds |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Second-degree atrioventricular block | disease of the electrical conduction system of the heart. It is a conduction block between the atria and ventricles. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Retinopathy of prematurity | disease of the eye affecting prematurely born babies generally having received intensive neonatal care, in which oxygen therapy is used on them due to the premature development of their lungs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Epiretinal membrane | disease of the eye in response to changes in the vitreous humor or more rarely, diabetes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Thygeson's superficial punctate keratopathy | disease of the eyes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Endometriosis | disease of the female reproductive system characterized by the growth of endometrial tissue outside the uterine body |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Occupational cardiovascular disease | disease of the heart and blood vessels caused by working conditions |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Reis–Bucklers corneal dystrophy | disease of the human eye |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Immune disorder | disease of the immune system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Monomelic amyotrophy | disease of the lower motor neurons |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Respiratory disease | disease of the respiratory system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Urologic disease | disease of the urinary system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tropical disease | disease prevalent in or unique to tropical and subtropical regions |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | HHV-8-associated MCD | disease subtype |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Alveolar lung disease | disease that affect the alveoli of the lungs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Rare disease | disease that affects a small percentage of the population |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Scrapie | disease that affects sheep and goats |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Laminitis | disease that affects the feet of hooved animals |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Coral disease | disease that afflicts corals |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Fish disease and parasites | disease that afflicts fish |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Poultry disease | disease that afflicts poultry |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Blood-borne disease | disease that can be spread through contamination by blood and other body fluids |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Multiple sclerosis | disease that damages the myelin sheaths around nerve axons |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Genetic disorder | disease that has material basis in genetic variations in the human genome |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Metabolic disorder | disease that involving errors in metabolic processes of building or degradation of molecules |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Airborne disease | disease that is caused by pathogens and transmitted through the air |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Aspartylglucosaminuria | disease that is characterized by a decline in mental functioning, accompanied by an increase in skin, bone and joint issues |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pulmonary insufficiency | disease that occurs when the pulmonary valve is not strong enough to prevent backflow into the right ventricle |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pacemaker syndrome | disease that represents the clinical consequences of suboptimal atrioventricular (AV) synchrony or AV dyssynchrony, regardless of the pacing mode, after pacemaker implantation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | List of types of malnutrition | disease that results from excessive or inadequate intake of food and nutrients |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Agraphia | disease that results in the loss of the ability to write |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Fecal–oral route | disease transmission via pathogens from fecal particles |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Favus | disease usually affecting the scalp, but occurring occasionally on any part of the skin, and even at times on mucous membranes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Kidney failure | disease where the kidneys fail to adequately filter waste products from the blood |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Acute (medicine) | disease with a rapid onset and/or a short course |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Idiopathic disease | disease with unknown pathogenesis or apparently spontaneous origin |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Epileptic seizure | disease, disturbance of cortical function due to a sudden, abnormal, excessive, and disorganized discharge of brain cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Anaplasmosis | disease, mostly animal (cattle) also in humans, caused by bacteria of the genus Anaplasma |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lifestyle disease | diseases linked with the way people live their life. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Xenophobia | dislike of that which is perceived to be foreign or strange |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Benign paroxysmal positional vertigo | disorder arising from a problem in the inner ear |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Protein S deficiency | disorder associated with increased risk of venous thrombosis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Psychoorganic syndrome | disorder characterised by impairment of memory, thought disorders etc., due to diffuse psychoorganic brain damage |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Catecholaminergic polymorphic ventricular tachycardia | disorder characterized by an abnormal heart rhythm (arrhythmia) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hydrocephalus | disorder characterized by an abnormal increase of cerebrospinal fluid in the ventricles of the brain |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Calcific tendinitis | disorder characterized by deposits of hydroxyapatite (a crystalline calcium phosphate) in any tendon of the body |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sydenham's chorea | disorder characterized by rapid, uncoordinated jerking movements primarily affecting the face, hands and feet |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Degenerative disease | disorder characterized by the progressive loss of function and/or structure of the affected tissues |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Autoimmune neutropenia | disorder common in infants and young children |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Wolff–Parkinson–White syndrome | disorder due to a specific type of problem with the electrical system of the heart which has resulted in symptoms |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gaming disorder | disorder due to addictive gaming behaviour |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Parental alienation syndrome | disorder in which a child, on an ongoing basis, belittles and insults one parent without justification, due to a combination of factors, including indoctrination by the other parent |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Plastic bronchitis | disorder in which branching casts of the airways are expectorated |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Laryngospasm | disorder in which the adductor muscles of the vocal cords exhibit increased activity leading to laryngeal spasm |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Low back pain | disorder involving muscles, nerves, bones of the back |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Benign paroxysmal vertigo of childhood | disorder of children which presents with recurrent episodes of dizzyness |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Environmental enteropathy | disorder of chronic intestinal inflammation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Persistent vegetative state | disorder of consciousness caused by severe brain damage |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lymphadenopathy | disorder of lymph nodes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Trigger finger | disorder of the finger |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mitral insufficiency | disorder of the heart in which the mitral valve does not close properly when the heart pumps out blood |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ménière's disease | disorder of the inner ear |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Asbestos-related diseases | disorder of the lung and pleura caused by the inhalation of asbestos fibres |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cherry eye | disorder of the nictitating membrane (NM), also called the third eyelid, present in the eyes of dogs and cats |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Thought disorder | disorder of thought form, content or stream |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Abdominal migraine | disorder primarily of children which presents with episodes of abdominal pain without an accompanying headache |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Epidermolysis bullosa simplex | disorder resulting from mutations in the genes encoding keratin 5 or keratin 14 |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bruxism | disorder that involves involuntarily grinding or clenching of the teeth |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ramsay Hunt syndrome type 2 | disorder that is caused by the reactivation of varicella zoster virus in the geniculate ganglion, a nerve cell bundle of the facial nerve |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Post-nasal drip | disorder that occurs when excessive mucus is produced by the nasal mucosa |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lipedema | disorder where there is enlargement of both legs due to deposits of fat under the skin |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Leptomeningeal cancer | disorder which occurs in approximately 5% of people with cancer in which the disease spreads to the membranes (meninges) surrounding the brain and spinal cord |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hematologic disease | disorder which primarily affects the blood |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Decompression illness | disorders arising from ambient pressure reduction |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ventricular fibrillation | disorganized electrical activity in the ventricles. It is a type of cardiac arrhythmia Ventricular fibrillation results in cardiac arrest |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Alice in Wonderland syndrome | disorienting neurological condition |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Fugue state | dissociative disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Depersonalization disorder | dissociative disorder in which the sufferer is affected by persistent or recurrent feelings of depersonalization and/or derealization |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hydrocolpos | distension of the vagina caused by accumulation of fluid due to congenital vaginal obstruction |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Fire breather's pneumonia | distinct type of exogenous lipoid pneumonia (chemical pneumonitis) that results from inhalation or aspiration of hydrocarbons of different types, such as lamp oil |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dysgeusia | distortion of the sense of taste; also often associated with ageusia, which is the complete lack of taste, and hypogeusia, which is a decrease in taste sensitivity |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Plagiocephaly | distortion of the skull |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mental disorder | distressing thought or behavior pattern |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Neurogenic shock | distributive type of shock resulting in low blood pressure, attributed to disruption of autonomic pathways within the spinal cord |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Balance disorder | disturbance that causes an individual to feel unsteady |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Myelodysplastic syndrome | diverse collection of hematological (blood-related) medical conditions that involve ineffective production of the myeloid class of blood cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chronic granulomatous disease | diverse group of hereditary diseases in which certain cells of the immune system have difficulty forming the reactive oxygen compounds used to kill certain ingested pathogens. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Alternobaric vertigo | dizzyness caused bu uneven pressure in the middle ears |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Oneiroid syndrome | dream-like fantastic delusional state (psychopathological syndrome) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ptosis (breasts) | drooping or sagging female breasts |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Salicylate sensitivity | drug allergy that has allergic trigger acetylsalicylic acid |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Barbiturate dependence | drug dependence that involves the continued use of barbiturates despite problems related to use of the substance |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cannabis use disorder | drug dependence that involves the continued use of cannabis despite problems related to use of the substance |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cocaine dependence | drug dependence that is a psychological dependency on the regular use of cocaine |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Drug reaction with eosinophilia and systemic symptoms | drug eruption characterized by high fever, erythematous rash and inflammation of internal organs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Extrapyramidal symptoms | drug-induced movement disorders |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Primary polydipsia | dry mouth and excessive fluid consumption in the absence of physiological stimuli to drink |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Selective immunoglobulin A deficiency | dysgammaglobulinemia characterized by a deficiency of immunoglobulin A |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Revesz syndrome | dyskeratosis congenita that has material basis in an X-linked recessive mutation of TINF2 on chromosome 14q12 |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Acrofrontofacionasal dysostosis | dysostosis characterized by intellectual disability, short stature, hypertelorism, broad notched nasal tip, cleft lip palate, postaxial camptobrachypolysyndactyly, fibular hypoplasia and anomalies of foot structure |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cenani–Lenz syndactylism | dysostosis characterized by syndactyly, malformation of the forearm and lower limb bones, renal hypoplasia or aplasia and that has material basis in homozygous or compound heterozygous mutation in the LRP4 gene on chromosome 11p11 |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Synostosis | dysostosis that results in abnormal fusing of adjacent bones |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Acrodysostosis | dysostosis that results in shortening of interphalangeal joints located in hand or located in foot along with mental deficiency |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Paroxysmal kinesigenic choreoathetosis | dystonia characterized by autosomal dominant inheritance of recurrent brief involuntary hyperkinesias triggered by sudden movements that has material basis in heterozygous mutation in the PRRT2 gene on chromosome 16p11 |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Myoclonic dystonia | dystonia characterized by myoclonic jerks affecting mostly proximal muscles and dystonia, usually torticollis or writer's cramp, that typically responds to alcohol and has onset in the first of second decade of life |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Focal dystonia | dystonia that is localized to a specific part of the body |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Torticollis | dystonic condition defined by an abnormal, asymmetrical head or neck position, which may be due to a variety of causes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Anorexia nervosa | eating disorder characterized by refusal to maintain a healthy body weight, and an obsessive fear of gaining weight due to a distorted self image |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bulimia nervosa | eating disorder that is characterized by a cycle of bulimia (binge eating) followed by inappropriate acts such as purging to avert weight gain |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hyalophagia | eating disorder that is characterized by an appetite for glass |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pica (disorder) | eating disorder that is characterized by an appetite for non-nutritive substances or food ingredients |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Rumination syndrome | eating disorder that is characterized by effortless regurgitation of most meals following consumption |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Alveolar hydatid disease | echinococcosis that is caused by the larvae of Echinococcus multilocularis affecting the liver as a slow growing, destructive tumor, with abdominal pain, biliary obstruction, and occasionally metastatic lesions into the lungs and brain |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cervical ectropion | ectropion |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Joint effusion | effusion of watery liquid into the cavity of a joint |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Occult fracture | effusion shoulder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sinoatrial block | electrical impulse is delayed or blocked on the way to the atria, thus delaying the atrial bea |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypophosphatemia | electrolyte disorder in which there is a low level of phosphate in the blood |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hyperphosphatemia | electrolyte disorder in which there is an elevated level of phosphate in the blood. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hyperkalemia | elevated level of potassium (K+) in the blood serum. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypertriglyceridemia | elevated levels of triglycerides in the blood |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Paradoxical embolism | embolus which is carried from the venous side of circulation to the arterial side, or vice versa |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Embryonal carcinoma | embryonal cancer that is a type of germ cell tumour that is located in the ovaries or located in the testes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Anxiety | emotion characterized by an unpleasant state of inner turmoil |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pleural empyema | empyema (an accumulation of pus) in the pleural cavity that can develop when bacteria invade the pleural space, usually in the context of a pneumonia |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Herpesviral encephalitis | encephalitis associated with herpes simplex virus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Arbovirus encephalitis | encephalitis diseases caused by an arbovirus infection |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Viral encephalitis | encephalitis that involves inflammation of the brain caused by viral infection |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Infective endocarditis | endocarditis that is characterized by inflammation of the endocardium caused by infectious agents. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Nonbacterial thrombotic endocarditis | endocarditis that results from the deposition of small sterile vegetations on valve leaflets |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Endocarditis | endocardium disease characterized by inflammation of the endocardium of the heart chambers and valves |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Endocardial fibroelastosis | endocardium disease that is characterized by a thickening of the inmost lining of the heart chambers due to an increase in the amount of supporting connective tissue and elastic fibers |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pancreatic cancer | endocrine gland cancer located in the pancreas |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Thyroid cancer | endocrine gland cancer located in the thryoid gland located in the neck below the thyroid cartilage |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Neuroendocrine tumor | endocrine gland cancer that has material basis in neuroendocrine cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pinealoma | endocrine gland located in the pineal gland located in the brain |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Adrenal adenoma | endocrine organ benign neoplasm, a benign tumor of the glandular type (adenoma) in the adrenal gland |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pancreatic disease | endocrine system disease that is located in the pancreas |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Postpartum depression | endogenous depression that involves intense, sustained and sometimes disabling depression experienced by women after giving birth |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Macroglossia | enlargement of the tongue |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Penetration (weaponry) | entrance of a projectile into a target |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tanganyika laughter epidemic | epidemic |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Brill–Zinsser disease | epidemic typhus that is a mild form of the disease, which recurs in someone after a long period of latency due to immunosuppression, malnutrition or other illnesses |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Localized epidermolysis bullosa simplex | epidermolysis bullosa simplex that is characterized by skin blistering that begins anytime between childhood and adulthood and is usually limited to the hands and feet |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Generalized epidermolysis bullosa simplex | epidermolysis bullosa simplex that is characterized by widespread blisters that appear at birth or in early infancy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dravet syndrome | epilepsy characterized by frequent febrile seizures and with onset before 1 year |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Photosensitive epilepsy | epilepsy characterized by seizures triggered by visual stimuli that form patterns in space or time, such as flashing lights |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Generalized epilepsy | epilepsy syndrome that is characterised by generalised seizures with no apparent cause which arise from many independent foci (multifocal epilepsies) or from epileptic circuits that involve the whole brain |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Focal seizure | epilepsy syndrome that is characterised by seizures that are preceded by an isolated disturbance of a cerebral function and arise from an epileptic focus, a small portion of the brain that serves as the irritant driving the epileptic response |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Curb (horse) | equine disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Esophageal achalasia | esophageal disease characterized by an inability of the esophagus to move food toward the stomach resulting from the lower esophogeal sphincter not fully relaxing during swallowing |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Eosinophilic esophagitis | esophagitis characterized by inflammation involving eosinophils located in esophagus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Barrett's esophagus | esophagus condition |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Seeing pink elephants | euphemism for drunken hallucination caused by alcoholic hallucinosis or delirium tremens |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Patulous Eustachian tube | eustachian tube disorder with a wider eustachian tube which allows a larger bolus of bacteria-laden material from the nasopharynx during an infection to enter the middle ear, causing a more fulminant infection |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Psychogenic non-epileptic seizure | events resembling an epileptic seizure, but without the characteristic electrical discharges associated with epilepsy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Paradoxical laughter | exaggerated expression of humour |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hyperesthesia | exaggerated sensations of tactile stimuli |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Childhood phobias | exaggerated, intense fear found in children |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Abdominal obesity | excessive abdominal fat around the stomach and abdomen |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypersexuality | excessive arousal and interest in sex |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Nosocomephobia | excessive fear of hospitals |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Vaginal yeast infection | excessive growth of yeast in the vagina that results in irritation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Polyphagia | excessive hunger or increased appetite |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Internet addiction disorder | excessive internet use that causes psychological disorders. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Computer addiction | excessive or compulsive use of the computer |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypersalivation | excessive production of saliva |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypersomnia | excessive sleep |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hereditary multiple exostoses | exostosis that has material basis in a mutation on the genes EXT1, EXT2 and EXT3 which results in multiple bony spurs throughout a child's growth |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Calcaneal spur | exostosis that results in an abnomal growth located in calcaneus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Breast engorgement | expansion and pressure exerted by the synthesis and storage of breast milk |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Paraphilia | experience of intense sexual arousal to atypical objects, situations, or individuals |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mycobacterial cervical lymphadenitis | extrapulmonary tuberculosis that is located in lymph node, and has symptom lymphadenopathy, has symptom fever, has symptom weight loss, has symptom fatigue, has symptom night sweats and has symptom cough |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tuberculous pericarditis | extrapulmonary tuberculosis that is located in pericardium resulting in acute pericarditis, chronic pericardial effusion, cardiac tamponade or pericardial constriction |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Urogenital tuberculosis | extrapulmonary tuberculosis that is located in urogenital system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Miliary tuberculosis | extrapulmonary tuberculosis that results in formation of tiny lesions in all the organs. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ancraophobia | extreme fear of wind or drafts |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Fecalith | extreme form of fecal impaction |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Batten disease | extremely rare and fatal autosomal recessive neurodegenerative disorder in humans |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Farber disease | extremely rare autosomal recessive lysosomal storage disease marked by a deficiency in the enzyme ceramidase |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Triploid syndrome | extremely rare chromosomal disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Fibrodysplasia ossificans progressiva | extremely rare connective tissue disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pyridoxine-dependent epilepsy | extremely rare disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | MOMO syndrome | extremely rare genetic disorder which belongs to the overgrowth syndromes and has been diagnosed in only six cases around the world, and occurs in 1 in 100 million births |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bagassosis | extrinsic allergic alveolitis that is an industrial disease characterized by cough, difficult breathing, chills, fever, and prolonged weakness caused by the inhalation of the dust of bagasse containing thermophilic actinomycetes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bird fancier's lung | extrinsic allergic alveolitis which is caused by inhalation of antigens from avian excreta, symptoms are abrupt onset of dyspnea, cough, malaise, and fever after exposure to antigen |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Myocarditis | extrinsic cardiomyopathy that is characterized as an inflammation of the heart muscle |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Acute posterior multifocal placoid pigment epitheliopathy | eye disease causing lesions in retina |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Coloboma | eye disease characterized by missing pieces of tissue in structures that form the eye, such as the iris, retina, choroid or optic disc |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pigment dispersion syndrome | eye disease characterized by slit-like depigmented areas of the iris with up to 50% of patients going on to develop gluacoma |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ptosis (eyelid) | eye disease characterized by the drooping or falling of the upper or lower eyelid |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Exophthalmos | eye disease that is characterized by a bulging of the eye anteriorly out of the orbit |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Glaucoma | eye disease that is characterized by an unstable or a sustained increase in the intraocular pressure which the eye cannot withstand without damage to its structure or impairment of its function |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ocular hypertension | eye disease that is characterized by elevated intraocular pressure in the absence of optic nerve damage or visual field loss |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Retinopathy | eye disease that is located in the retina |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Microphthalmia | eye disease where one or both eyeballs are abnormally small |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | White dot syndromes | eye diseases |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Blepharochalasis | eyelid disease that is characterized by exacerbations and remissions of eyelid edema, which results in a stretching and subsequent atrophy of the eyelid tissue, leading to the formation of redundant folds over the lid margins |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Blepharitis | eyelid disease that is characterized by often chronic inflammation of the eyelid, generally the part where eyelashes grow |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Proboscis (anomaly) | facial anomaly |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bell's palsy | facial paralysis resulting from dysfunction in the cranial nerve VII (facial nerve) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Agenesis | failure of an organ to develop during embryonic growth |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Nondisjunction | failure of chromatid or chromosome pairs to separate |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Circulatory collapse | failure of circulation, such as blood flow |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Anismus | failure of the normal relaxation of pelvic floor muscles during attempted defecation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lipoprotein lipase deficiency | familial hyperlipemia characterized by a deficiency of the enzyme lipoprotein lipase and the subsequent build up of chylomicrons and increased plasma concentration of triglycerides |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Familial hypercholesterolemia | familial hyperlipidemia characterized by very high levels of low-density lipoprotein (LDL) and early cardiovascular disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Seafood allergy | family of food allergies caused by seafood |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ventricular tachycardia | fast heart rhythm that originates in one of the ventricles of the heart |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sudden unexpected death in epilepsy | fatal complication of epilepsy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hungerford massacre | fatal shooting of 16 people in Hungerford, U.K. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Stress fracture | fatigue-induced fracture of the bone caused by repeated stress over time |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Focal fatty liver | fatty liver can be cure on early stage by taking medicine |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Non-alcoholic fatty liver disease | fatty liver disease characterized by the storing of excess fat in liver cells which is is not caused by heavy alcohol use |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Entomophobia | fear for insects |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Whorephobia | fear of and discrimination against sex workers |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Myrmecophobia | fear of ants |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Balloon phobia | fear of balloons |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Fear of bats | fear of bats |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pogonophobia | fear of beards |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Frigophobia | fear of becoming too cold |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Taphophobia | fear of being buried alive |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Philophobia (fear) | fear of being in love and falling in love |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Scopophobia | fear of being seen or stared at by others |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Stir crazy (condition) | fear of being trapped in a future of boredom |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ailurophobia | fear of cats |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Coulrophobia | fear of clowns |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cyberphobia | fear of computers |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mageiricophobia | fear of cooking |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Decidophobia | fear of decision making |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Demonophobia | fear of demons |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Oneirophobia | fear of dreams |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pyrophobia | fear of fire |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gamophobia | fear of getting married or being in a relationship |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gerontophobia | fear of growing old, or a hatred or fear of the elderly |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cephalalgiaphobia | fear of headaches |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hippopotomonstrosesquipedaliophobia | fear of long words |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mechanophobia | fear of machines |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Telephone phobia | fear of making or taking phone calls |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Atelophobia | fear of not being good enough or imperfection |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Genuphobia | fear of one's own knees or someone else's knees or the act of kneeling |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Coprophobia | fear of or aversion to feces or defecation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Phonophobia | fear of or aversion to loud sounds |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Toxiphobia | fear of poisons and being poisoned |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Glossophobia | fear of public speaking or of speaking in general |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sexophobia | fear of sexual organs or sexual activities and, in a larger sense, the fear of sexuality |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Genophobia | fear of sexual relations or sexual intercourse |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ostraconophobia | fear of shellfish |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Afrophobia | fear of the cultures and peoples of Africa, as well as the African diaspora |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Phallophobia | fear of the erect penis or excessive aversion to masculinity |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Triskaidekaphobia | fear of the number 13 |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Thalassophobia | fear of the sea or of sea travel |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Medication phobia | fear of the use of pharmacological treatments |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hodophobia | fear of travel |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Spheksophobia | fear of wasps |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Vermiphobia | fear of worms |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ephebiphobia | fear of youth |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chromophobia | fear of, or aversion to, colors |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hedonophobia | fear or aversion to obtaining pleasure |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Herpetophobia | fear or aversion to reptiles |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Neophobia | fear or dislike of new things |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bibliophobia | fear or hatred of books |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Aporophobia | fear or hostility towards poor people |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Fear of God | fear or respect for the Deity |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Thought insertion | feeling as if one's thoughts are not one's own, but rather belong to someone else and have been inserted into one's mind |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Foreign language anxiety | feeling of unease and insecurity experienced in learning or using a foreign language |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cat flu | feline upper respiratory tract disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Fallopian tube cancer | female reproductive organ cancer that is located in fallopian tube |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ovarian cancer | female reproductive organ cancer that is located in the ovary |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Uterine cancer | female reproductive organ cancer that is located in the uterus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Vaginal cancer | female reproductive system cancer that is located in the vagina |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ectopic pregnancy | female reproductive system disease characterized by the implantation of the embryo outside the uterine cavity |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Eisenmenger's syndrome | fetal heart defect |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Navel fetishism | fetish for belly-buttons |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Fetus in fetu | fetus-like tissue mass within a fetus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Monostotic fibrous dysplasia | fibrous dysplasia of bone involving only one bone |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Velvet (fish disease) | fish disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Rectovaginal fistula | fistula or abnormal connection between the rectum and the vagina |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Photopsia | flashes of light |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Glaukomflecken | flecks in the lens of the eye caused by glaucoma |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pulmonary edema | fluid accumulation in the air spaces and parenchyma of the lungs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Nipple bleb | fluid filled blister on the nipple |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ovarian cyst | fluid-filled sac in the ovary |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Writer's cramp | focal dystonia that affects a single muscle or small group of muscles in the hand resulting from involuntary muscular contractions |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Spasmodic dysphonia | focal dystonia that involves the muscles that control the vocal cords, resulting in strained or breathy speech |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Oculogyric crisis | focal dystonia that is characterized by a prolonged involuntary upward deviation of the eyes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Oromandibular dystonia | focal dystonia that is characterized by distortions of the mouth and tongue. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Blepharospasm | focal dystonia that is characterized by the involuntary, forcible contraction of the muscles controlling eye blinks |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Speech and language impairment | fonoaudiologia |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Egg allergy | food allergy that is an allergy or hypersensitivity to dietary substances from the yolk or whites of eggs, causing an overreaction of the immune system which may lead to severe physical symptoms |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Paragonimiasis | food-borne parasitic infection caused by the lung fluke, most commonly Paragonimus westermani |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Toxic oil syndrome | foodborne illness |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Scombroid food poisoning | foodborne illness that typically results from eating spoiled fish |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Diabetic foot | foot that exhibits any pathology that results directly from diabetes mellitus or any long-term complication of diabetes mellitus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Behavioral addiction | form of addiction that involves a compulsion to engage in a rewarding non-drug-related behavior despite any negative consequences to the person's physical, mental, social or financial well-being |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Autotopagnosia | form of agnosia |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Functional hypothalamic amenorrhea | form of amenorrhea caused by hypogonadism related to defective functioning of the hypothalamus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Isolated atrial amyloidosis | form of amyloidosis affecting the atria of the heart |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Abdominal pregnancy | form of an ectopic pregnancy where the embryo or fetus is growing and developing outside the womb in the abdomen, but not in the Fallopian tube, ovary or broad ligament |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hemolytic anemia | form of anemia due to hemolysis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sneddon's syndrome | form of arteriopathy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Atherosclerosis | form of arteriosclerosis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Osteoarthritis | form of arthritis caused by degeneration of joints |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Restrictive cardiomyopathy | form of cardiomyopathy in which the walls are rigid,and the heart is restricted from stretching and filling with blood properly |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Non-progressive congenital ataxia | form of cerebellar ataxia which can occur with or without cerebellar hypoplasia. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Psychological dependence | form of dependence that involves emotional–motivational withdrawal symptoms upon cessation of drug use or exposure to a stimulus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Type 1 diabetes | form of diabetes mellitus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Primordial dwarfism | form of dwarfism that results in a smaller body size in all stages of life |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Focal dermal hypoplasia | form of ectodermal dysplasia |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Subdural empyema | form of empyema in the subdural space |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Eosinophilic fasciitis | form of fasciitis, the inflammatory diseases that affect the fascia, the connective tissues surrounding muscles, blood vessels and nerves |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Calculus (dental) | form of hardened dental plaque |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Choristoma | form of heterotopia closely related benign tumors, found in abnormal locations. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Transient hypogammaglobulinemia of infancy | form of hypogammaglobulinemia appearing after birth, leading to a reduction in the level of IgG, and also sometimes IgA and IgM |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Arthritis | form of joint disorder that involves inflammation of one or more joints |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Contrast-induced nephropathy | form of kidney damage in which there has been recent exposure to medical imaging contrast material |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Overnutrition | form of malnutrition in which the intake of nutrients is oversupplied |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Acute myeloblastic leukemia | form of myeloid leukemia affecting myeloblasts |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Fat necrosis | form of necrosis characterized by the action upon fat by digestive enzymes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Colic | form of pain |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hepatic porphyria | form of porphyria in which the enzyme deficiency occurs in the liver |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Striae gravidarum | form of scarring of the skin of the abdominal due to sudden weight gain during pregnancy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Marasmus | form of severe malnutrition characterized by energy deficiency |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Aquaphilia (fetish) | form of sexual fetishism |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Object sexuality | form of sexuality focused on particular inanimate objects |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Binswanger's disease | form of small vessel vascular dementia caused by damage to the white brain matter |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Exotropia | form of strabismus where the eyes are deviated outward |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ordinal linguistic personification | form of synesthesia in which ordered sequences, such as ordinal numbers, days, months and letters are associated with personalities and/or genders |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Paroxysmal tachycardia | form of tachycardia which begins and ends in an acute (or paroxysmal) manner |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Anaplastic thyroid cancer | form of thyroid cancer |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pancreatic injury | form of trauma sustained by the pancreas |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Liver injury | form of trauma sustained to the liver |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Scrub typhus | form of typhus caused by the intracellular parasite Orientia tsutsugamushi |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cortical visual impairment | form of visual impairment caused by a brain problem |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Formicophilia | form of zoophilia |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Deep vein thrombosis | formation of a blood clot (thrombus) in a deep vein |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Maria and Teresa Tapia | former conjoined twins from the Dominican Republic |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Spinal fracture | fracture affecting the vertebrae of the spinal column |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bennett's fracture | fracture of the base of the first metacarpal bone |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Colles' fracture | fracture of the distal radius bone |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Radial head fracture | fracture of upper end of radius |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Salter–Harris fracture | fracture that involves the epiphyseal plate or growth plate of a bone |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bad trip | frightening and unpleasant experience triggered by psychoactive drugs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Autosomal dominant nocturnal frontal lobe epilepsy | frontal lobe epilepsy that is characterized by autosomal dominant inheritance with childhood onset of clusters of brief nocturnal motor seizures with hyperkinetic or tonic manifestations |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Distal radius fracture | frykman VII |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chronic diarrhea of infancy | functional diarrhea of childhood |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Eyespot (wheat) | fungal disease of wheat |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Candidiasis | fungal infection due to any type of Candida |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mycosis | fungal infection of animals, including humans |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tinea barbae | fungal infection of the hair |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Onychomycosis | fungal infection of the nail |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dermatophytosis | fungal infection of the skin |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tinea incognita | fungal skin infection caused by the presence of a topical immunosuppressive agent |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Corn grey leaf spot | fungus-caused disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Webbed toes | fusion of toes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Trichomoniasis | gagoparasitic protozoa infectious disease that is caused by the parasites Trichomonas vaginalis or Trichomonas tenax |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Foot drop | gait abnormality |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Galactokinase deficiency | galactosemia that involves an accumulation of galactose and galactitol secondary to the decreased conversion of galactose to galactose-1-phosphate by galactokinase |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Biliary dyskinesia | gallbladder disease characterized by altered tonus of the sphincter of Oddi, disturbance in the coordination of contraction of the biliary ducts, and/or reduction in the speed of emptying of the biliary tree |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Succinic semialdehyde dehydrogenase deficiency | gamma-amino butyric acid metabolism disorder that is characterized by a deficiency of succinic semialdehyde dehydrogenase resulting in elevated levels of gamma-hydroxybutyric acid |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Superior mesenteric artery syndrome | gastro-vascular disorder in which the third and final portion of the duodenum is compressed between the abdominal aorta (AA) and the overlying superior mesenteric artery |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Viral gastroenteritis | gastroenteritis caused by a virus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pleomorphic adenoma | gastrointestinal benign neoplasm that is a located in the salivary glands |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Esophageal cancer | gastrointestinal system cancer that is located in the esophagus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Oral cancer | gastrointestinal system cancer that is located in the oral cavity |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Stomach cancer | gastrointestinal system cancer that is located in the stomach |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Liver cancer | gastrointestinal system cancer, located in the liver |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mucositis | gastrointestinal system disease that is characterized by painful inflammation and ulceration of the mucous membranes lining the digestive tract |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Esophageal disease | gastrointestinal system disease that is located in the esophagus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gallbladder disease | gastrointestinal system disease that is located in the gallbladder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Enteropathy | gastrointestinal system disease that is located in the intestine |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | List of hepato-biliary diseases | gastrointestinal system disease that is located in the liver and/or biliary tract |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Oral and maxillofacial pathology | gastrointestinal system disease that is located in the mouth |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Stomach disease | gastrointestinal system disease that is located in the stomach. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Empyema | gathering of pus within a naturally existing anatomical cavity |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Isobutyryl-coenzyme A dehydrogenase deficiency | gene (11q25) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Progressive osseous heteroplasia | gene (20q13.2-q13.3), coding for guanine nucleotide-binding proteins. POH can, however, be distinguished clinically by the deep and progressive nature of the heterotopic bone formation. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | 2-Methylbutyryl-CoA dehydrogenase deficiency | gene (located on chromosome 10q25-26) have been reported in affected patients. Treatment includes carnitine supplementation and a low-protein diet. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | D-Glyceric acidemia | gene has been mapped to 3p21 |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Platyspondylic lethal skeletal dysplasia, Torrance type | gene. Although PLSD-T is generally lethal, survival to adulthood has been reported in two families. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypertensive encephalopathy | general brain dysfunction due to significantly high blood pressure |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dizziness | general term for a number of types of impairment in spatial perception and stability |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Otitis | general term for inflammation or infection of the ear |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Myoclonic astatic epilepsy | generalised idiopathic epilepsy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Generalized lymphadenopathy | generalised lymphadenites |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Intellectual disability | generalized neurodevelopmental disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Absence seizure | generalized seizure characterized by a brief loss and return of consciousness, generally not followed by a period of lethargy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypochromic anemia | generic term for any type of anemia in which the red blood cells (erythrocytes) are paler than normal |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Genetic predisposition | genetic characteristic which influences the possible phenotypic development of an individual organism within a species or population |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | XYY syndrome | genetic condition in which a male has an extra Y chromosome. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ciliopathy | genetic disease associated with mutations encoding defective proteins, which result in either abnormal function formation or function of cilia |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Maturity onset diabetes of the young | genetic disease that has material basis in mutations in the MODY genes disrupting insulin production |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Malignant hyperthermia | genetic disease that is characterized by a drastic and uncontrolled increase in skeletal muscle oxidative metabolism, which overwhelms the body's capacity to supply oxygen, remove carbon dioxide, and regulate body temperature |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Oral-facial-digital syndrome | genetic disease that is characterized by malformations of the face, oral cavity, and digits with polycystic kidney disease and variable involvement of the central nervous system and has material basis in X-linked inheritance of an OFD gene |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Coffin–Siris syndrome | genetic disease that is characterized by underdevelopment of the tips of fingers or toes, underdevelopment or abscense of finger or toe nails and developmental disability |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Equine polysaccharide storage myopathy | genetic disorder in Quarter Horses and draft horses |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Liddle's syndrome | genetic disorder inherited in an autosomal dominant manner that is characterized by early, and frequently severe, high blood pressure |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Marfan syndrome | genetic disorder of the connective tissue |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Incontinentia pigmenti | genetic disorder that affects the skin, hair, teeth, nails, and central nervous system. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Coffin–Lowry syndrome | genetic disorder that is X-linked dominant |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Alpha-1 antitrypsin deficiency | genetic disorder that may result in lung disease or liver disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Norrie disease | genetic disorder that primarily affects the eye and almost always leads to blindness |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hurler syndrome | genetic disorder that results in the buildup of glycosaminoglycans (AKA GAGs, or mucopolysaccharides) due to a deficiency of alpha-L iduronidase |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dopamine-responsive dystonia | genetic movement disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Brachydactyly type D | genetic trait |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hereditary spastic paraplegia | genetically and clinically heterogeneous group of neurodegenerative disorders characterized by progressive spasticity and hyperreflexia of the lower limbs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Diphallia | genital medical condition |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Koro (medicine) | genital-related neurosis, in which an individual has an overpowering belief that one’s genitalia are retracting and will disappear, despite the lack of any true longstanding changes to the genitals |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Campylobacteriosis | genus of Gram-negative bacteria |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Trophoblastic neoplasm | germ cell and embryonal cancer that derives from trophoblastic tissue |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Teratoma | germ cell and embryonal cancer that is an encapsulated tumor with tissue or organ components resembling normal derivatives of all three germ layers |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dysgerminoma | germ cell cancer that derives from cells that give rise to egg cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Endodermal sinus tumor | germ cell cancer that has material basis in cells that line the yolk sac of the embryo |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Germinoma | germ cell cancer that lacks histologic differentiation. It usually refers to a tumor in the brain |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Seminoma | germinoma that has material basis in cells that make sperm and eggs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Giant-cell tumor of bone | giant cell tumor and bone cancer and bone tissue neoplasm that results in the presence of multinucleated giant cells (osteoclast-like cell) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sadomasochism | giving or receiving of pleasure from acts involving the receipt or infliction of pain or humiliation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Astroblastoma | glial tumor derived from the astroblast, a type of cell that closely resembles spongioblastoma and astrocytes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Endophthalmitis | globe disease that is characterized by inflammation of the inside of the eye |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mesangial proliferative glomerulonephritis | glomerulonephritis associated primarily with the mesangium |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | IgA nephropathy | glomerulonephritis characterized by build up of IgA antibody in the glomerulus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Glomerulosclerosis | glomerulonephritis that is characterized by hardening of the glomerulus in the kidney |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lupus nephritis | glomerulonephritis that is characterized by inflammation of the kidneys resulting from systemic lupus erythematosus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Non-celiac gluten sensitivity | gluten-related disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Glycogen storage disease | glycogen metabolism disorder that has material basis in enzymes deficiencies necessary in the processing of glycogen synthesis or breakdown within muscles, liver, and other cell types |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Glycogen storage disease type IX | glycogen storage disease characterized by deficiency of hepatic phosphorylase kinase activity |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Multinodular goitre | goiter characterized by a multinodular enlargement of the thyroid gland |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | XY gonadal dysgenesis | gonadal dysgenesis that is characterized by a normal 46,XY karyotype along with a progressive loss of germ cells on the developing gonads of an embryo |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | XX gonadal dysgenesis | gonadal dysgenesis that is characterized by the lack of functional ovaries to induce puberty in an otherwise 46,XX female |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ectromelia | gross hypo- or aplasia of long bones or limbs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sick sinus syndrome | group of abnormal heart rhythms (arrhythmias) presumably caused by a malfunction of the sinus node, the heart's primary pacemaker |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Transmissible spongiform encephalopathy | group of brain diseases that are characterized by brain damage resulting from the abnormal folding, clumping and accumulation of cellular proteins in the brain induced by prion proteins |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Leukemia | group of cancers that usually begin in the bone marrow |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Heart arrhythmia | group of conditions in which the heartbeat is irregular, too fast, or too slow |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Fetal alcohol spectrum disorder | group of conditions that can occur in a person whose mother drank alcohol during pregnancy. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Transposition (birth defect) | group of congenital defects involving an abnormal spatial arrangement |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Transposition of the great vessels | group of congenital heart defects involving an abnormal spatial arrangement of any of the great vessels: superior and/or inferior venae cavae, pulmonary artery, pulmonary veins, and aorta |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Severe congenital neutropenia | group of diseases that affect myelopoiesis, causing a congenital form of neutropenia |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Frontotemporal lobar degeneration | group of disorders |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Spinocerebellar ataxia | group of dominantly inherited, predominately late-onset, cerebellar ataxias |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ehlers–Danlos syndromes | group of genetic connective tissue disorders |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Distal muscular dystrophy | group of genetic disorders characterized by progressive muscular atrophy and muscle weakness beginning in the hands, the legs, or the feet |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lipodystrophy | group of genetic or acquired disorders in which the body is unable to produce and maintain healthy fat tissue |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Typhus | group of infectious diseases |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mucolipidosis | group of inherited metabolic diseases characterized by the accumulation of acid mucopolysaccharides, sphingolipids or glycolipids in visceral and mesenchymal cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Interstitial lung disease | group of lung diseases affecting the interstitium (the tissue and space around the air sacs of the lungs) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Substance-related disorder | group of mental and behavioural disorders, including both substance dependence and substance abuse |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Jerusalem syndrome | group of mental phenomena |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Diabetes | group of metabolic disorders characterized by high blood sugar levels over a prolonged period |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Trematodiases | group of parasitoses |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Zellweger spectrum disorders | group of rare autosomal recessive genetic disorders |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ichthyosis hystrix | group of rare skin disorders in the ichthyosis family of skin |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Olivopontocerebellar atrophy | group of sporadic and inherited neurodegenerative disorders affecting the cerebellum, pons, and inferior olives |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hemangioendothelioma | group of vascular neoplasms |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Viral hemorrhagic fever | group of viral diseases having in common capillary permeability, leukopenia and thrombocytopenia |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Silver–Russell syndrome | growth disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Psychosocial short stature | growth disorder that is observed between the ages of 2 and 15, caused by extreme emotional deprivation or stress |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Desmoplasia | growth of fibrous or connective tissue |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypertrichosis | hair disease characterized by hair growth that is abnormal in quantity or location |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypotrichosis | hair disease that is characterized by sparse hair on the scalp resulting from abnormal hair follicle development and has material basis in mutations in proteins involved in hair growth, division or proliferation of cells within hair follicles |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hirsutism | hair growth on a woman, generally causing a full beard to grow (see bearded lady) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pattern hair loss | hair loss due to susceptibility of hair follicles to androgenic miniaturization |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pilonidal disease | hair-containing cyst or sinus, occurring chiefly in the coccygeal region |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mushroom poisoning | harmful effects from ingestion of toxic substances present in a mushroom |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lycopenemia | harmless skin condition caused by excessive ingestion of red foods |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Transmisogyny | hatred or dislike of trans women or girls |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Biphobia | hatred, irrational fear, or mistreatment of bisexual people |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Transphobia | hatred, irrational fear, prejudice, or discrimination against transgender people |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Overweight | having more body fat than is optimally healthy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Head and neck squamous-cell carcinoma | head and neck carcinoma that has material basis in squamous cells that line the moist, mucosal surfaces inside the head and neck |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Trigeminal autonomic cephalgia | headache disorder characterized by episodes of unilateral, short lasting pain and associated ipsilateral cranial autonomic symptoms |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Eye disease | health condition negatively affecting the eye |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Long-term effects of alcohol consumption | health effects of drinking alcoholic beverages |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hyperacusis | hearing disorder characterized by a sensitivity to sound |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Auditory neuropathy | hearing disorder characterized by impaired transmission of signals through the auditory nerve, resulting in mild to severe hearing loss and poor speech perception |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Unilateral hearing loss | hearing impairment |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Occupational hearing loss | hearing loss caused by occupational hazards |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Yentl Syndrome | heart attack symptoms in women |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Right bundle branch block | heart block in the electrical conduction system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Brugada syndrome | heart conduction disease that is characterized by abnormal electrocardiogram (ECG) findings and an increased risk of sudden cardiac death |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Short QT syndrome | heart conduction disease that is characterized by heart arrhythmia defined as a short QT interval on an EKG (less than 300 ms) that does not significantly change with heart rate, tall and peaked T waves, and a structurally normal heart |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Atrioventricular block | heart conduction disease that is characterized by the impairment of the conduction between the atria and ventricles of the heart |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypertensive heart disease | heart disease that is caused by high blood pressure |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Constrictive pericarditis | heart disorder in which the pericardial sac becomes thickened and fibrotic, tightening the myocardium and impeding the normal myocardial function |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Commotio cordis | heart injury |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sinus tachycardia | heart rate greater than 100 beats/min (bpm) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tachycardia | heart rate that exceeds the normal resting rate |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bradycardia | heart rate that is below the normal range |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bigeminy | heart rhythm problem in which there is a continuous alternation of long and short heart beats |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ventricular septal defect | heart septal defect characterized by an opening in the interventricular septum, causing a shunt between ventricles |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Taussig–Bing syndrome | hearth disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Obstetrical bleeding | heavy bleeding in pregnancy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Glomus tumor | hemangiopericytic tumor that is a mesenchymal neoplasm composed of cells that closely resemble the modified smooth muscle cells of the normal glomus body |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lymphoma | hematologic cancer that affects lymphocytes that reside in the lymphatic system and in blood-forming organs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mastocytoma | hematologic cancer that has material basis in mast cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Breus' mole | hematoma formed in uterus in pregnancy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Myeloproliferative neoplasm | hematopoietic disorders that derive from the blood-forming stem cells of the bone marrow |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hereditary elliptocytosis | hematopoietic system disease characterized by oval or elliptical red blood cells, slight or absent hemolysis with little or no anemia; splenomegaly is often present |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Alternating hemiplegia of childhood | hemiplegia characterized by recurrent episodes of temporary weakness or complete paralysis on one or both sides of the body |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | African iron overload | hemochromatosis characterized by a predisposition to iron loading that is exacerbated by excessive intake of dietary iron, commonly related to consumption of tradition beer brewed in non-galvanized steel drums |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Juvenile hemochromatosis | hemochromatosis characterized by autosomal recessive inheritance of early onset of severe iron loading with symptoms including; hypogonadotropic hypogonadism, cardiomyopathy, arthropathy, and liver fibrosis or cirrhosis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Haemochromatosis type 3 | hemochromatosis that has material basis in homozygous or compound heterozygous mutation in the TFR2 gene on chromosome 7q22 |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bolivian hemorrhagic fever | hemorrhagic fever and zoonotic infectious disease originating in Bolivia after infection by Machupo virus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Activated protein C resistance | hemostatic disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hepatic veno-occlusive disease | hepatic vascular disease that is characterized by obstruction of some of the small veins of the liver |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Alcoholic hepatitis | hepatitis (inflammation of the liver) due to excessive intake of alcohol |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Viral hepatitis | hepatitis that involves viral infection causing inflammation of the liver |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Megalencephalic leukoencephalopathy with subcortical cysts | hereditary CNS demyelinating disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Episodic ataxia | hereditary ataxia characterized by sporadic bouts of ataxia with or without continuous muscle movement |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Autosomal recessive cerebellar ataxia type 1 | hereditary ataxia that has material basis in autosomal recessive inheritance |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Familial dysautonomia | hereditary sensory and autonomic neuropathy type III (HSAN-III), is a disorder of the autonomic nervous system which affects the development and survival of sensory |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Abdallat–Davis–Farrage syndrome | hereditary spastic paraplegia that has material basis in variation in the chromosome region 1q24-q32 |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | MASA syndrome | hereditary spastic paraplegia that is characterized by hydrocephalus, spasticity of the lower limbs, adducted thumbs, aphasia, seizures, agenesis of the corpus callosum and intellectual disability in the mild to moderate range |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypercalcaemia | high calcium (Ca2+) level in the blood serum |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Benzodiazepine overdose | high doses of benzodiazepines and the side effects |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypercholesterolemia | high levels of cholesterol in the blood |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Marek's disease | highly contagious viral neoplastic disease in chickens |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Histidinemia | histidine metabolism disease that involves a deficiency of the enzyme histidase |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Langerhans cell sarcoma | histiocytic and dendritic cell cancer that derives from the lymph nodes, derives from the skin, derives from the liver, derives from the spleen and derives from bones |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Interdigitating dendritic cell sarcoma | histiocytic and dendritic cell cancer that effect dendritic cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Brewer infarcts | histological finding found in renal disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bright's disease | historical classification of nephritis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Functioning tumor | hormone producing endocrine neoplasm, associated with a hormonal syndrome |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hormone receptor positive breast tumor | hormone receptor positive breast tumor |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Equine infectious anemia | horse disease caused by a retrovirus and transmitted by bloodsucking insects |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Glanders | horse disease that can be transmitted to humans |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Covering sickness | horses disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cystitis | human Disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Botulism | human and animal disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bubonic plague | human and animal disease; plague involving the lymphatic system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Urinary tract infection | human and animal infection |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Leptospirosis | human and animal infectious disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Birt–Hogg–Dubé syndrome | human autosomal dominant genetic disorder that can cause susceptibility to kidney cancer, renal and pulmonary cysts |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tongue thrust | human behavioral pattern |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Erythroblastopenia | human desease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Yersiniosis | human disease caused by any bacteria of the genus Yersinia |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Whooping cough | human disease caused by the bacteria Bordetella pertussis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Shingles | human disease caused by varicella zoster |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gaucher's disease | human disease characterized by deficiency of the enzyme glucocerebrosidase which results in the accumulation of harmful quantities of the glycolipid glucocerebroside throughout the body |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pancreatitis | human disease involving the inflammation of the pancreas |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Periodontal disease | human disease of the tissues surrounding the teeth |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | HIV/AIDS | human disease resulting from HIV infection |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pleural disease | human disease, lung disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Enthesopathy | human disease: a disorder involving the attachment of a tendon or ligament to a bone |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Proctitis | human disease; inflammation of the anus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Oppositional defiant disorder | human disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hyperemesis gravidarum | human disorder of pregnancy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Flat feet | human foot arch that is very low |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chronic condition | human health condition or disease that is persistent or otherwise long-lasting in its effects |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bipolar disorder | human mental illness characterized by mood changes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Epilepsy | human neurological disease causing seizures |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tardive dyskinesia | human neurological disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Amoebiasis | human protozoa disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pustulosis | human skin disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Rubella | human viral disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Familial hypocalciuric hypercalcemia | hypercalcemia characterized byautosomal dominant inheritance with elevation of serum calcium levels and decreased urinary calcium excretion |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hyper-IgM syndrome type 4 | hyperimmunoglobulin syndrome characterized by normal or increased serum IgM concentrations associated with low or absent serum IgG, IgA, and IgE concentrations, indicating a defect in the class-switch recombination (CSR) process |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sclerosteosis | hyperostosis characterized by excessive bone formation most prominent in the skull, mandible, clavicle, ribs and diaphyses of long bones; bone formation occurs throughout life |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Worth syndrome | hyperostosis that has material basis in a mutation in the LRP5 gene which results in increased bone density and bony structures located in palate |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Exostosis | hyperostosis that involves formation of new bone on the surface of preexisting bone |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hyperthecosis | hyperplasia of the theca interna of the ovary |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Food allergy | hypersensitivity reaction type I disease that is an abnormal response to a food, triggered by the body's immune system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Latex allergy | hypersensitivity reaction type I disease triggered by latex |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | IPEX syndrome | hypersensitivity reaction type II disease characterized by onset in infancy of refractory diarrhea, endocrinopathies, type 1 diabetes mellitus, and dermatitis that has material basis in mutation in the FOXP3 gene on chromosome Xp11 |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Vitiligo | hypersensitivity reaction type II disease that causes depigmentation of patches of skin resulting from loss of function or death of melanocytes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sjögren syndrome | hypersensitivity reaction type II disease that involves attack of immune cells which destroy the exocrine glands that produce tears and saliva |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Goodpasture syndrome | hypersensitivity reaction type II disease that is characterized by glomerulonephritis located in kidney and hemorrhaging located in lung |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Autoimmune heart disease | hypersensitivity reaction type II disease that is the abnormal functioning of the immune system that causes your immune system to produce antibodies or T cells against cells and/or tissues in the cardiovascular system. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sarcoidosis | hypersensitivity reaction type IV disease characterized by the growth of collections of inflammatory cells (granulomas) in multiple organs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cryoglobulinemia | hypersensitivity reaction type IV disease that involves large amounts of cryoglobulins in the blood which become thick or gel-like in cold temperatures |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Heavy chain disease | hypersensitivity reaction type IV disease that results from a proliferation of cells producing immunoglobulin heavy chains |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cutaneous small-vessel vasculitis | hypersensitivity vasculitis that results in inflammation of small blood vessels, characterized clinically by palpable purpura, which is a slightly elevated purpuric rash over one or more areas of the skin |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pulmonary hypertension | hypertension characterized by an increase of blood pressure in the pulmonary artery, pulmonary vein or pulmonary capillaries |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Portal hypertension | hypertension in the hepatic portal system, which are the portal vein and its branches, which drain from most of the intestines to the liver |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pre-eclampsia | hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Essential hypertension | hypertension with no known cause, the most common type of hypertension |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Potomania | hypo-osmolality syndrome related to massive consumption of beer |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gonadal dysgenesis | hypogonadism that is characterized by a progressive loss of germ cells on the developing gonads of an embryo |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypobetalipoproteinemia | hypolipoproteinemia characterized by permanently low levels of apolipoprotein B and LDL cholesterol resulting from an impaired ability to absorb and transport fats |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pelizaeus–Merzbacher disease | hypomyelinating leukodystrophy characterized by impaired myelin formation, nystagmus, spastic quadriplegia, ataxia, and developmental delay that has material basis in mutation in the PLP1 gene on chromosome Xq22 |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Adrenocorticotropic hormone deficiency | hypopituitarrium that is characterized by a decreased or absent production of adrenocorticotropic hormone by the pituitary gland |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Adiposogenital dystrophy | hypothalamic disease that is characterized by endocrine dysfunction of the hypothalamic gland resulting in delayed puberty, small testes, and obesity |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Congenital hypothyroidism | hypothyroidism that is present at birth |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Conjoined twins | identical twins joined in utero |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Generalized epilepsy with febrile seizures plus | idiopathic generalized epilepsy that is characterized by febrile seizures often with accessory afebrile generalized tonic-clonic seizures with childhood onset |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Desquamative interstitial pneumonia | idiopathic interstitial pneumonia that is characterized by the accumulation of bronchiolocentric alveolar macrophages in alveolar spaces and interstitial inflammation and involves mild bronchiolar fibrosis and chronic inflammation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Insulitis | illness |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Latrodectism | illness caused by the bite of Latrodectus spiders (the black widow spider and related species) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Coturnism | illness featuring muscle tenderness and rhabdomyolysis after consuming quail that have fed on poisonous plants |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Toxocariasis | illness of humans caused by larvae (immature parasitic worms) of the dog roundworm (Toxocara canis), the cat roundworm (Toxocara cati) or the fox roundworm (Toxocara canis) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Foodborne illness | illness resulting from food that is spoiled or contaminated by pathogenic bacteria, viruses, parasites, or toxins |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cervical spine disorder | illness that affects the cervical spine, which is made up of the upper first seven vertebrae, encasing and shielding the spinal cord |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cocaine intoxication | immediate effects of cocaine on the body |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Common variable immunodeficiency | immune disorder characterized by recurrent infections and low antibody levels, specifically in immunoglobulin |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lymphatic disease | immune system disease that is located in the lymphatic system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Primary immunodeficiency | immune system disease that results when one or more essential parts of the immune system is missing or not working properly at birth due to a genetic mutation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Allergy | immune system response to a substance that most people tolerate well |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | X-linked severe combined immunodeficiency | immunodeficiency disorder in which the body produces very few T cells and NK cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Nephrogenic diabetes insipidus | impaired renal function disease characterized by a complete or partial resistance of the kidneys to vasopressin (ADH) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Amotivational syndrome | impairements associated with cannabis use |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Paraplegia | impairment in motor or sensory function of the lower extremities |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Visual agnosia | impairment in recognition of visually presented objects |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Claudication | impairment in walking, or pain, discomfort or tiredness in the legs that occurs during walking and is relieved by rest |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Impetigo herpetiformis | impetigo that is characterized as a form of severe pustular psoriasis occurring in pregnancy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pyromania | impulse control disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Intermittent explosive disorder | impulse control disorder that involves the episodic inability to control violent impulses with a disproportionate degree of aggressiveness |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Kleptomania | impulse control disorder that involves the repeated impulse to steal for no great gain, when he or she has sufficient money to pay for the item and no need for what is stolen |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Trichotillomania | impulse control disorder that involves the uncontrollable plucking of ones hair |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Implant (Scientology) | in Scientology |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Spatial disorientation | inability of a person to correctly determine his/her body position in space |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Infertility | inability of a person, animal or plant to reproduce by natural means that is no intervention of contraceptive techniques |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Color blindness | inability or decreased ability to see colour, or perceive colour differences, under normal lighting conditions |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Visuospatial dysgnosia | inability to analyse and orient using visual representations and their spatial relationships |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Male infertility | inability to father a child |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Paragrammatism | inability to form grammatically correct sentences |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Avolition | inability to initiate and persist in goal-directed activities (negative symptom) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Fecal incontinence | inability to refrain from defecation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Source amnesia | inability to remember how information was acquired while still retaining the knowledge |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Auditory arrhythmia | inability to replicate musical or rhythmic patterns |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hemeralopia | inability to see clearly in bright light and is the exact opposite of Nyctalopia |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Insomnia | inability to sleep peacefully |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Muteness | inability to speak, often caused by a speech disorder or mental disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Aphasia | inability to use spoken language |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Respiratory failure | inadequate gas exchange by the respiratory system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hereditary fructose intolerance | inborn error of fructose metabolism caused by a deficiency of the enzyme aldolase B |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hyperplasia | increase in the amount of organic tissue that results from cell proliferation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Monocytosis | increase in the number of monocytes circulating in the blood |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypertrophy | increase in the volume of an organ or tissue due to the enlargement of its component cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hyperaemia | increase of blood flow to different tissues in the body |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Puberty menorrhagia | increased menstrual flow soon after puberty |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Proventricular dilatation disease | incurable disease of psittacine birds |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Terminal illness | incurable disease unable to be treated that will almost certainly result in the patient's death |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Feline infectious peritonitis | incurable, fatal disease that affects cats |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sensitization (immunology) | induction of an adaptive response in the immune system, either for immunization to disease or as allergy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Benign familial infantile epilepsy | infancy electroclinical syndrome that is characterized by convulsions, with onset at age 3 to 12 months |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Epilepsy-intellectual disability in females | infantile epileptic encephalopathy that has material basis in the gene encoding protocadherin-19 (PCDH19) on chromosome Xq22 |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Salpingitis | infection and inflammation in the fallopian tubes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Klebsiella pneumonia | infection by Klebsiella bacteria |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pneumocystosis | infection by Pneumocystis jirovecii, that primarily occurs as a pulmonary infection AIDS patients |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Genital herpes | infection by herpes simplex virus (HSV) of the genitals |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Anthrax | infection caused by Bacillus anthracis bacteria |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cyclosporiasis | infection caused by Cyclospora cayetanensis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Salmonellosis | infection caused by Salmonella bacteria |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cryptic infection | infection caused by an as yet unidentified pathogen |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Swine influenza | infection caused by any one of several types of swine influenza viruses |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Vertically transmitted infection | infection caused by pathogens that uses mother-to-child transmission |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chikungunya | infection caused by the chikungunya virus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Streptococcal pharyngitis | infection of the back of the throat including the tonsils caused by group A streptococcus (GAS) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Japanese encephalitis | infection of the brain caused by the Japanese encephalitis virus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dacryocystitis | infection of the lacrimal sac |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Parasitic pneumonia | infection of the lungs with parasites, commonly by parasitic worms |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pyonephrosis | infection of the renal collecting system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pelvic inflammatory disease | infection of uterus, fallopian tubes, ovaries or the inner surface of pelvis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Puerperal mastitis | infection related to having children in women |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Necrotizing fasciitis | infection that results in the death of the body's soft tissue |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sexually transmitted infection | infection transmitted through human sexual behavior |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Transfusion transmitted infection | infection with a patogen through a transfusion to a recipient |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Erysipeloid | infections most commonly present in a mild cutaneous |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pneumococcal infection | infections with bacteria of the species streptococcus pneumoniae |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Foot-and-mouth disease | infectious and sometimes fatal viral disease that affects cloven-hoofed animals and caused by apthovirus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Zika fever | infectious arboviral disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Blackleg (disease) | infectious bacterial disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Nocardiosis | infectious disease affecting either the lungs (pulmonary nocardiosis) or the whole body (systemic nocardiosis) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lyme disease | infectious disease caused by Borrelia bacteria, spread by ticks |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Influenza | infectious disease caused by an influenza virus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Clonorchiasis | infectious disease caused by the Chinese liver fluke, Clonorchis sinensis, and two related species |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tuberculosis | infectious disease caused by the bacterium Mycobacterium tuberculosis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Parasitic disease | infectious disease caused or transmitted by a parasite |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Feline infectious anemia | infectious disease found in felines |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Emerging infectious disease | infectious disease novel in its outbreak range or transmission mode |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Aspergillosis | infectious disease of humans, birds and other animals |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Surra | infectious disease of mammals, caused by Trypanosoma |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Carrion's disease | infectious disease produced by Bartonella bacilliformis infection |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Zoonosis | infectious disease that is transmitted between species (sometimes by a vector) from animals other than humans to humans or from humans to other animals |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Keratoconjunctivitis | inflammation ("-itis") of the cornea and conjunctiva. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Neurogenic inflammation | inflammation arising from the local release by afferent neurons of inflammatory mediators such as Substance P, Calcitonin Gene-Related Peptide (CGRP), neurokinin A (NKA), and endothelin-3 (ET-3) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Granuloma | inflammation consisting of immune cells known as macrophages |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sialadenitis | inflammation of a salivary gland |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dactylitis | inflammation of an entire digit (a finger or toe) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Osteitis | inflammation of bone |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Systemic lupus erythematosus | inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sycosis | inflammation of hair follicles, |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Endometritis | inflammation of inner lining of uterus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Meningitis | inflammation of membranes around the brain and spinal cord |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Viral meningitis | inflammation of meninges by viruses |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sacroiliitis | inflammation of pelvis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Microvasculitis | inflammation of small blood vessels |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Adenoiditis | inflammation of the adenoid tissue |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Syphilitic aortitis | inflammation of the aorta |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Aortitis | inflammation of the aortic wall |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Appendicitis | inflammation of the appendix |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Encephalomyelitis | inflammation of the brain and spinal cord |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mastitis | inflammation of the breast |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chorioretinitis | inflammation of the choroid |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Colitis | inflammation of the colon or the large intestine |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Epiglottitis | inflammation of the epiglottis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Esophagitis | inflammation of the esophagus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ophthalmia | inflammation of the eye |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tenosynovitis | inflammation of the fluid-filled sheath (called the synovium) that surrounds a tendon, typically leading to joint pain, swelling, and stiffness |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dysentery | inflammation of the intestine causing diarrhea with blood |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Nephritis | inflammation of the kidneys |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Laryngitis | inflammation of the larynx |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cheilitis | inflammation of the lips |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hepatitis | inflammation of the liver tissue |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chemical pneumonitis | inflammation of the lung caused by aspirating or inhaling irritants |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Stomatitis | inflammation of the mouth and lips |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sinusitis | inflammation of the mucous membrane that lines the sinuses resulting in symptoms |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Catarrh | inflammation of the mucous membranes in one of the airways or cavities of the body |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Conjunctivitis | inflammation of the outermost layer of the eye and the inner surface of the eyelids |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Peritonitis | inflammation of the peritoneum, the lining of the inner wall of the abdomen |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypophysitis | inflammation of the pituitary gland |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Autoimmune hypophysitis | inflammation of the pituitary gland due to autoimmunity |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Orchitis | inflammation of the testes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tracheitis | inflammation of the trachea |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mastitis in dairy cattle | inflammation of the udder in cows |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Omphalitis of newborn | inflammation of the umbilical cord stump |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Non-gonococcal urethritis | inflammation of the urethra |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cervicitis | inflammation of the uterine cervix |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Atrophic vaginitis | inflammation of the vagina due to the thinning and shrinking of the tissues, as well as decreased lubrication |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Spondylitis | inflammation of the vertebra |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Arteritis | inflammation of the walls of arteries, usually as a result of infection or autoimmune response. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bumblefoot (infection) | inflammation on birds' and rodents' feet |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lymphangitis | inflammation or an infection of the lymphatic channels that occurs as a result of infection at a site distal to the channel |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ileitis | inflammatory bowel disease characterized by inflammation located in ileum, has symptom diarrhea, has symptom abdominal pain, often in the right lower quadrant, has symptom weight loss |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ulcerative colitis | inflammatory bowel disease that causes ulcers in the colon |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pneumonia | inflammatory condition of the lung |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Anti-MOG associated encephalomyelitis | inflammatory demyelinating disease previously considered part of the multiple sclerosis spectrum |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Neuromyelitis optica | inflammatory demyelinating diseases of the central nervous system characterized mainly by attacks of uni- or bilateral optic neuritis and acute myelitis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mediastinitis | inflammatory process affecting the mediastinum |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Type III hypersensitivity | inflammatory response resulting from recognition of immune complexes via complement or Fc receptors on effector cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Avian influenza | influenza caused by viruses adapted to birds |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Canine influenza | influenza occurring in canine animals |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Medulloblastoma | infratentorial cancer that is located in the lower part of the brain and is a type of primitive neuroectodermal tumor |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Scott syndrome | inherited blood coagulation disease characterized by autosomal recessive inheritance of hemorrhagic episodes due to impaired platelet coagulant activity that has material basis in homozygous mutation in the TMEM16F gene on chromosome 12q12 |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Antithrombin III deficiency | inherited blood coagulation disease characterized by the tendency to form clots in the veins |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Epidermolysis bullosa dystrophica | inherited disease affecting the skin and other organs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cowden syndrome | inherited disorder causing tumor-like growth and increased cancer risk |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Medullary cystic kidney disease | inherited form of cystic kidney disease leading to fibrosis and impaired renal function that is caused by mutations in the UMOD gene, which encodes uromodulin/Tamm-Horsfall mucoprotein |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | GRACILE syndrome | inherited metabolic disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Inborn errors of purine–pyrimidine metabolism | inherited metabolic disorder involving dysfunction of purine and pyrimidine metabolism |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Inborn errors of carbohydrate metabolism | inherited metabolic disorder that affect the catabolism and anabolism of carbohydrates |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lysosomal storage disease | inherited metabolic disorder that involve an abnormal accumulation of substances inside the lysosome resulting from defects in lysosomal function |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hereditary hyperbilirubinemia | inherited metabolic disorder that involves elevated levels of bilirubin resulting from disruption of bilirubin metabolism |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Inborn errors of metal metabolism | inherited metabolic disorder that involves metabolic disturbances in the processing or distribution of dietary minerals |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Peroxisomal disorder | inherited metabolic disorder that involves peroxisome malfunction |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cone dystrophy | inherited ocular disorder characterized by the loss of cone cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypoactivity | inhibition of behavioral or locomotor activity |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chronic phase chronic myelogenous leukemia | initial phase of chronic myeloid leukemia consisting of an relatively indolent period lasting from 4 to 7 years |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cerebrospinal fluid leak | injury |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Snakebite | injury caused by a bite from a snake |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Patellar dislocation | injury of the knee |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Scapular fracture | injury of the shoulder blade |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Shin splints | injury or pain in the lower tibia |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Strain (injury) | injury to a muscle in which the muscle fibers tear as a result of overstretching |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Blunt cardiac injury | injury to the heart as the result of blunt trauma |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Aortic dissection | injury to the innermost layer of the aorta allows blood to flow between the layers of the aortic wall, forcing the layers apart |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Repetitive strain injury | injury to the musculoskeletal and nervous systems that may be caused by repetitive tasks, forceful exertions, vibrations, mechanical compression, or sustained or awkward positions |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Spinal cord injury | injury to the spine on the back side of humans |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Superior canal dehiscence syndrome | inner ear disease characterized by dehiscence in the bone overlying the superior semicircular canal experience with symptoms of pressure or sound-induced vertigo, bone conduction hyperacusis, and pulsatile tinnitus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | African horse sickness | insect-borne reovirus infection of horses, mules and donkeys in Africa and the Middle East; characterized by pulmonary edema, cardiac involvement, and edema of the head and neck |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gigantiform cementoma | instance of ossifying fibroma (disease) that is caused by an inherited modification of the individual's genome |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Steroid diabetes | insulin and steroid treatment |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hair disease | integumentary system disease that is located in hair |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Nail disease | integumentary system disease that is located in nail |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Renpenning's syndrome | intellectual disability that is characterized by small head size (microcephaly), long narrow face, short stature, small testes, and intellectual deficit which follows X-linked inheritance and presents most often in males |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Anti-Catholicism | intense dislike or fear of Catholicism, hostility or prejudice towards Catholics |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Islamophobia | intense dislike or fear of Islam, hostility or prejudice towards Muslims |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Beatlemania in the United Kingdom | intense fan frenzy directed towards the English rock band the Beatles in the United Kingdom |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pulmonary contusion | internal bruise of the lungs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Arterial embolism | interruption of blood flow to an organ |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Myocardial infarction | interruption of blood supply to a part of the heart |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pneumoconiosis | interstitial lung disease that is caused by the inhalation of dust |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Balkan endemic nephropathy | interstitial nephritis endemic to the regions along the Danube river, in the modern countries of Croatia, Bosnia and Herzegovina, Serbia, Romania and Bulgaria |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Appendix cancer | intestinal cancer that is located in the appendix |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Small intestine cancer | intestinal cancer that is located in the small intestine |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Blind loop syndrome | intestinal disease characterized by a dysbalance of the bacterial flora of the small intestine, causing derangement to the normal physiological processes of digestion and absorption |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Inguinal hernia | intestinal disease characterized by a protrusion of abdominal cavity contests through the inguinal canal |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Inflammatory bowel disease | intestinal disease characterized by inflammation located in all parts of digestive tract |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Umbilical hernia | intestinal disease characterized by the protrusion by part of the intestine though an opening in the abdominal muscles |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Intestinal infectious diseases | intestinal disease that involves intestinal infection that has material basis in viruses, bacteria, fungi and parasites |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Enteritis | intestinal infectious disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Intracranial berry aneurysm | intracranial aneurysm with a characteristic rounded shape; the most common form of cerebral aneurysm |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Progressive familial intrahepatic cholestasis | intrahepatic cholestasis characterized by early onset of chronic unremitting cholestasis of hepatocellular origin that progresses to hepatic fibrosis, cirrhosis, and end-stage liver disease before adulthood |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Intrahepatic cholestasis of pregnancy | intrahepatic cholestasis characterized by reversible cholestasis typically occurring in the second or third trimester of pregnancy, elevated serum aminotransferases and bile acid level and resolution of symptoms by 2 to 3 weeks after delivery |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Intraparenchymal hemorrhage | intraparenchymal |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Noncompaction cardiomyopathy | intrinsic cardiomyopathy characterized by distinctive (spongy) morphological appearance of the LV myocardium |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dilated cardiomyopathy | intrinsic cardiomyopathy that is characterized by an an enlarged heart and damage to the myocardium causing the heart to pump blood inefficiently |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Arrhythmogenic cardiomyopathy | intrinsic cardiomyopathy that is characterized by hypokinetic areas involving the free wall of the right ventricle, with fibrofatty replacement of the right ventricular myocardium, with associated arrhythmias originating in the right ventricle |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Choreoathetosis | involuntary movements in a combination of chorea (irregular migrating contractions) and athetosis (twisting and writhing) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tremor | involuntary muscle contraction |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pseudohallucination | involuntary sensory experience vivid enough to be regarded as a hallucination, but recognised by the patient not to be the result of external stimuli |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypnic jerk | involuntary twitches |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hemosiderosis | iron metabolism disease that has material basis in an accumulation of hemosiderin, an iron-storage complex, resulting in iron overload |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ornithophobia | irrational fear of birds |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chemophobia | irrational fear of chemicals |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Necrophobia | irrational fear of dead things as well as things associated with death |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Rhinitis | irritation and inflammation of the mucous membrane inside the nose |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pruritus ani | irritation of the skin of the anus, causing itching |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Savant syndrome | is a condition in which someone with mental disabilities demonstrates certain abilities |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dysbaric osteonecrosis | ischemic bone disease caused by decompression bubbles in bone |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Osteochondrosis | ischemic bone disease that results in necrosis followed by regrowth in children and teens located in bone |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Osteochondritis dissecans | ischemic bone disease that results_in necrosis located_in epiphysis. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ischemic optic neuropathy | ischemic injury to the optic nerve |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pancreatic neuroendocrine tumor | islet cell tumor that has material basis in epithelial cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Wandering atrial pacemaker | it is an atrial arrhythmia that occurs when the natural cardiac pacemaker site shifts between the sinoatrial node, the atria, and/or the atrioventricular node. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gnathitis | jaw inflammation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pigmented villonodular synovitis | joint disease characterized by inflammation and overgrowth of the joint lining |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Spondyloarthropathy | joint disease of the vertebral column |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Parakeratosis | keratinization characterized by the retention of nuclei in the stratum corneum |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Herpes simplex keratitis | keratitis of the cornea that has material basis in herpes simplex type infection |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Palmoplantar keratoderma | keratosis characterized by abnormal thickening of the palms and the soles |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cholesteatoma | keratosis characterized by keratinizing squamous epithelium located in middle ear and/or mastoid, subepithelial connective tissue and by the progressive accumulation of keratin debris with or without surrounding inflammatory reaction |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mesoblastic nephroma | kidney cancer that is found in the kidney and is usually found before birth by ultrasound or within the first 3 months of life |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Focal segmental glomerulosclerosis | kidney disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Clear-cell sarcoma of the kidney | kidney sarcoma that has material basis in clear cells that are characterized as cells that look clear when viewed under a microscope |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Parasystole | kind of arrhythmia caused by the presence and function of a secondary pacemaker in the heart, which works in parallel with the SA node |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hemoglobinopathy | kind of genetic defect that results in abnormal structure of one of the globin chains of the hemoglobin |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Acral lentiginous melanoma | kind of lentiginous skin melanoma |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Milk sickness | kind of poisoning |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Yunnan sudden death syndrome | label used to define unexplained cases of cardiac arrest in villagers in Yunnan, China; now known to be caused by ingestion of the toxic mushroom Trogia venenata |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Inferiority complex | lack of self-worth, a doubt and uncertainty about oneself, and feelings of not measuring up to standards |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Anuria | lack of urine |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Metabolic acidosis | lactic acidosis that has material basis in high levels of acid |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Developmental language disorder | language abilities below the expected level for a given age |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Palilalia | language disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Paraphasia | language output error commonly associated with aphasia, and characterized by the production of unintended syllables, words, or phrases during the effort to speak |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Anal cancer | large intestine cancer that is located in the anus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Laryngeal cleft | laryngo-tracheo-esophageal cleft (LC) is a congenital malformation characterized by an abnormal, posterior, sagittal communication between the larynx and the pharynx, possibly extending downward between the trachea and the esophagus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pontiac fever | legionellosis that involves a milder respiratory illness without pneumonia. Symptoms include fever, headache and muscle aches which last for 2 to 5 days |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Legionnaires' disease | legionellosis that is characterized by severe form of infection producing pneumonia. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cutaneous leishmaniasis | leishmaniasis that involves skin infection caused by Leishmania species, resulting in one or more cutaneous lesions |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Caprine arthritis encephalitis | lentiviral infection in goats that can lead to chronic disease of joints and, rarely, encephalitis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tuberculoid leprosy | leprosy that results in one erythematous large plaque with well-defined borders that are elevated and that slope down into an atrophic center |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Borderline leprosy | leprosy that results in small numerous red irregularly shaped plaques |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lethal congenital contracture syndrome | lethal congenital contracture syndrome that has material basis in homozygous or compound heterozygous mutation in the mRNA export mediator GLE1 on chromosome 9q34 |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Necrotising hepatopancreatitis | lethal epizootic disease of farmed shrimp |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hydrops-ectopic calcification-moth-eaten skeletal dysplasia | lethality and affected fetuses are considered as nonviable |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Acute megakaryoblastic leukemia | leukemia that derives from blood-forming tissue in which megakaryocytes proliferate in the bone marrow and circulate in the blood in large numbers |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Acute lymphoblastic leukemia | leukemia that is characterized by over production of lymphoblasts. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Myeloid leukemia | leukemia that is located in myeloid tissue |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Childhood leukemia | leukemia that occurs in children |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lymphocytopenia | leukopenia that is the condition of having an abnormally low level of lymphocytes in the blood |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lichen planus | lichen disease that is located in skin, located in tongue or located in oral mucosa, which presents itself in the form of papules, lesions or rashes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Traumatic aortic rupture | life-threatening injury to the aorta |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sepsis | life-threatening organ dysfunction triggered by infection |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Anterior cruciate ligament injury | ligament injury near the knee |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Denture-related stomatitis | lip disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Carnitine palmitoyltransferase II deficiency | lipid metabolism disorder characterized by an enzymatic defect that prevents long-chain fatty acids from being transported into the mitochondria |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Barth syndrome | lipid metabolism disorder that has material basis in X-linked inheritance of the tafazzin gene and is characterized by decreased production of an enzyme required to produce cardiolipin |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Inborn errors of steroid metabolism | lipid metabolism disorder that involves defects in steroid metabolism |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Medium-chain acyl-coenzyme A dehydrogenase deficiency | lipid metabolism disorder that is characterized by a deficiency of the enzyme medium chain acyl-CoA dehydrogenase that results in the inability to convert medium chain fatty acids to energy, particularly during fasting |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Short-chain acyl-coenzyme A dehydrogenase deficiency | lipid metabolism disorder that is characterized by deficiency of the enzyme short chain acyl-CoA dehydrogenase that results in the inability to convert short chain fatty acids |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Very long-chain acyl-coenzyme A dehydrogenase deficiency | lipid metabolism disorder that is characterized by deficiency of the enzyme very long chain acyl-CoA dehydrogenase that results in the inability to convert very long chain fatty acids |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Fatty liver disease | lipid storage disease characterized by the accumulation of large vacuoles of triglyceride fat in liver cells via the process of steatosis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Neutral lipid storage disease | lipid storage disease that is characterized by accumulation of triglycerides in the cytoplasm of leukocytes, muscle, liver, fibroblasts, and other tissues |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Carotid-cavernous fistula | lipodystrophy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Familial partial lipodystrophy | lipodystrophy characterized by abnormal subcutaneous adipose tissue distribution beginning in late childhood or early adult life |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chondroid lipoma | lipoma that is a deep-seated, firm, yellow tumors that characteristically occur on the legs of women |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Angiolipoma | lipoma that is a painful subcutaneous nodule, having all other features of a typical lipoma |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Spindle cell lipoma | lipoma that is an asymptomatic, slow-growing subcutaneous tumor that has a predilection for the posterior back, neck, and shoulders of older men |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pleomorphic lipoma | lipoma that is characterized by floret giant cells with overlapping nuclei |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Liposarcoma | lipomatous cancer that arises in fat cells in deep soft tissue retroperitoneum |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Norman–Roberts syndrome | lissencephaly that has_material_basis_in homozygous mutation in the gene encoding reelin (RELN) on chromosome 7q22. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hepatocellular carcinoma | liver carcinoma that has material basis in undifferentiated hepatocytes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Primary biliary cholangitis | liver cirrhosis characterized by chronic and slow progressive destruction of intrahepatic bile ducts |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hematoma | localized collection of blood outside the blood vessels |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Periapical abscess | localized collection of pus associated with a tooth |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Abscess | localized collection of pus that has built up within the tissue of the body |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Coeliac disease | long term autoimmune disorder causing intolerance to gluten |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Myotonic dystrophy | long term genetic disorder that affects muscle function |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dementia | long-term brain disorders causing personality changes and impaired memory, reasoning, and normal function |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Parkinson's disease | long-term degenerative neurological disorder that mainly affects movement |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Asthma | long-term disease involving inflamed airways |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cirrhosis | long-term disease of the liver |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chromoblastomycosis | long-term fungal infection of the skin and subcutaneous tissue |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Rosacea | long-term human skin disease characterized by ruddy reddening of the skin |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Seborrhoeic dermatitis | long-term skin disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Diarrhea | loose or liquid bowel movements |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Runner's diarrhea | loose or liquid bowel movements while running |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Postpartum bleeding | loss of blood following childbirth |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Developmental regression | loss of developmental skills, as manifested by loss of developmental milestones |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Functio laesa | loss of function or disturbance of function |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hair loss | loss of hair from the head or body |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Retrograde amnesia | loss of memory of events that in occurred before the onset of amnesiac condition |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Paralysis | loss of muscle function for one or more muscles |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Anterograde amnesia | loss of the ability to create new memories after the onset of amnesia |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pure alexia | loss of the power to comprehend written materials despite preservation of the ability to write |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Acid erosion | loss of tooth structure due to chemical dissolution by acids not of bacterial origin |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypovolemia | low blood volume |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Subependymal giant cell astrocytoma | low-grade astrocytic brain tumor (astrocytoma) that arises within the ventricles of the brain |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Overbite | lower jaw being too far behind the upper jaw or a misalignment of the teeth |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bronchospasm | lower respiratory tract disease that affects the airways leading into the lungs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mucinous cystadenocarcinoma of the lung | lung adenocarcinoma that is a very rare malignant mucus-producing neoplasm arising from the uncontrolled growth of transformed epithelial cells originating in lung tissue |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Squamous-cell carcinoma of the lung | lung cancer |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Adenocarcinoma in situ of the lung | lung cancer that derives from the distal bronchioles or alveoli that initially exhibit a specific non-invasive growth pattern |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Giant-cell carcinoma of the lung | lung carcinoma that is located in large undifferentiated cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Alveolitis | lung disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lung abscess | lung disease characterized by microbial infection which causes a type of liquefactive necrosis of the pulmonary tissue and formation of cavities containing necrotic debris or fluid |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bronchiolitis obliterans | lung disease involving obstruction of the bronchioles |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pulmonary alveolar proteinosis | lung disease that is characterized by abnormal accumulation of surfactant occurs within the alveoli, interfering with gas exchange |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Drug-induced lupus erythematosus | lupus erythematosus caused by chronic use of certain drugs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Persistent generalized lymphadenopathy | lymph node disease characterized by enlarged, non-painful lymph nodes occurring for more than three to six months for which no other reason can be found |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lymphangiosarcoma | lymphatic system cancer that has material basis in endothelial cells located in lymphatic vessels |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Histiocytosis | lymphatic system disease that is characterized by an excessive number of histiocytes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Milroy's disease | lymphedema commonly located in legs, caused by congenital abnormalities in the lymphatic system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chronic lymphocytic leukemia | lymphoblastic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Thyroid lymphoma | lymphoma primarily involving the thyroid gland |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lymphoblastic lymphoma | lymphoma that has material basis in immature malignant lymphocytes (lymphoblasts) committed to the B-cell or T-cell lineage and located in primarily lymph nodes or located in extranodal sites |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gray zone lymphoma | lymphoma that is characterized by having cellular features of both classic Hodgkin's lymphomas and large B-cell Lymphomas |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hodgkin's lymphoma | lymphoma that is marked classically by the presence of Reed-Sternberg cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | X-linked lymphoproliferative disease | lymphoproliferative disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Castleman disease | lymphoproliferative syndrome characterized by one or more enlarged lymph nodes containing cells with hyaline-vascular, plasmacytic, or mixed appearance microscopically |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sialuria | lysosomal storage disease characterized by increased sialic acid in the urine |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Alpha-mannosidosis | lysosomal storage disease that has material basis in deficiency of the alpha-D-manosidase enzyme resulting in the impairment of cell function from a build up of complex sugars derived from glycoproteins in the lysosome |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Beta-mannosidosis | lysosomal storage disease that has material basis in deficiency of the beta-A-manosidase enzyme resulting in the disruption of N-linked glycoprotein oligosaccharide catabolism. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mucopolysaccharidosis | lysosomal storage disease that involves the accumulation of glycosaminoglycans in the tissues and their excretion in the urine |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lipid storage disorder | lysosomal storage disease that involves the accumulation of harmful amounts of lipids (fats) in some of the body's cells and tissues |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Megaloblastic anemia | macrocytic anemia that is characterized by inhibition of DNA synthesis during red blood cell production |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Helminthiasis | macroparasitic disease in which a part of the body is infected with parasitic worms |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ancylostomiasis | macroparasitic disease of humans and animals in which a part of the body is infected with parasitic worms known as ankylostoids. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Diabetic foot ulcer | major complication of diabetes mellitus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Psychotic depression | major depressive episode that is accompanied by psychotic symptoms |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Personality disorder | maladaptive patterns of behavior |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Babesiosis | malaria-like parasitic disease caused by infection with Babesia, a genus of Apicomplexa |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Adipomastia | male breast tissue enlargement solely due to excess fatty tissue |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Globozoospermia | male infertility characterized by round-headed spermatozoa lacking an acrosome |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Azoospermia | male infertility disease characterized by the absence of any measurable level of sperm in semen |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Prostate cancer | male reproductive cancer |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Testicular cancer | male reproductive system cancer that is located in the testicles |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lymphangioma | malformations of the lymphatic system characterized by lesions that are thin-walled cysts |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Angiosarcoma | malignant Vascular tumor that results in rapidly proliferating, extensively infiltrating anaplastic cells derives from blood vessels and derived from the lining of irregular blood-filled spaces |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ependymal tumor | malignant glioma that is derived from ependymal cells, a type of glial cell, located in ventricle lining within the central part of the brain |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Melanoma | malignant neoplasm originating from melanocytes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Secondary malignant neoplasm | malignant neoplasm that arises from a pre-existing lower grade lesion, or as a result of a primary lesion that has spread to secondary sites, or due to a complication of a cancer treatment |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Leiomyosarcoma | malignant smooth muscle cancer that can arise almost anywhere in the body, but is most common in the uterus, abdomen, or pelvis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Medullary thyroid cancer | malignant thyroid neoplasm originating from C-cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Protein–energy malnutrition | malnutrition defined as a range of pathological conditions arising from lack of dietary protein and energy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Breech birth | malpresentation of the fetus at near term or during labor with the fetal cephalic pole in the fundus of the uterus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Delayed ejaculation | man's inability for or persistent difficulty in achieving orgasm, despite typical sexual desire and sexual stimulation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Manganism | manganese poisoning |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bibliomania | mania |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sensory loss | many types of sense loss occur due to a dysfunctional sensation process, whether it be ineffective receptors, nerve damage, or cerebral impairment. Unlike agnosia, these impairments are due to damages prior to the perception process |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Splenic marginal zone lymphoma | marginal zone B-cell lymphocyte located in the spleen comprised of B-cells in place of white pulp |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Nodal marginal zone B cell lymphoma | marginal zone B-cell lymphoma which morphologically resembles lymph nodes involved by marginal zone lymphomas of extranodal or splenic types, but without evidence of extranodal or splenic disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | 2016 Munich shooting | mass shooting on 22 July 2016, in Munich, Germany |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Burkitt's lymphoma | mature B-cell neoplasm of B-cells found in the germinal center |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Peripheral T-cell lymphoma | mature T-cell and NK-cell lymphoma includes a group of T-cell lymphomas that develop away from the thymus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | MODY 2 | maturity-onset diabetes of the young that has material basis in heterozygous mutation in the GCK gene on chromosome 7p13 |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Choking | mechanical obstruction of the flow of air from the environment into the lungs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Presbyopia | medical condition associated with aging of the eye |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Blastocystosis | medical condition caused by infection with Blastocystis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Periostitis | medical condition caused by inflammation of the periosteum, a layer of connective tissue that surrounds bone |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Stannosis | medical condition caused by inhalation of tin compounds |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Occupational asthma | medical condition caused or exacerbated by the workplace |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hyperandrogenism | medical condition characterized by excessive levels of androgens in the body |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Epididymitis | medical condition characterized by inflammation of the epididymis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gastroenteritis | medical condition characterized by inflammation of the stomach and/or small intestine |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pseudobulbar palsy | medical condition characterized by the inability to control facial movements (such as chewing and speaking) and caused by a variety of neurological disorders |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Adenomyosis | medical condition characterized by the presence of glandular tissue in muscle |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Anasarca | medical condition characterized by widespread swelling |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypertrophic osteoarthropathy | medical condition combining clubbing and periostitis of the small hand joints |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Recurrent pyogenic cholangitis | medical condition especially common in Asians |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Egg binding | medical condition in birds or other egg-laying animals, where the female is unable to pass an egg that has formed |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Obesity | medical condition in which excess body fat harms health |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Auto-brewery syndrome | medical condition in which intoxicating quantities of ethanol are produced within the digestive system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Raynaud syndrome | medical condition in which spasm of arteries cause episodes of reduced blood flow |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Microcephaly | medical condition in which the brain does not develop properly resulting in a smaller than normal head |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Entropion | medical condition in which the eyelid (usually the lower lid) folds inward |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Paraphimosis | medical condition in which the foreskin of a penis becomes trapped behind the glans penis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cardiomegaly | medical condition in which the heart is enlarged |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Third-degree atrioventricular block | medical condition in which the impulse generated in the sinoatrial node (SA node) in the atrium of the heart does not propagate to the ventricles |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ectropion | medical condition in which the lower eyelid turns outwards |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hematocolpos | medical condition in which the vagina fills with menstrual blood |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dryness (medical) | medical condition in which there is a decrease in normal lubrication of the skin or mucous membranes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pancytopenia | medical condition in which there is a reduction in the number of red and white blood cells, as well as platelets |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Anisomastia | medical condition in which there is a severe asymmetry or unequalness in the size of the breasts |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bone fracture | medical condition in which there is physical damage to the continuity of the bone |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chronic fatigue syndrome | medical condition involving extreme fatigue and a wide host of other neurological symptoms. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Acute tubular necrosis | medical condition involving the death of tubular epithelial cells that form the renal tubules of the kidneys |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Disorders of sex development | medical condition involving the reproductive system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Aphonia | medical condition leading to loss of voice |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypertensive kidney disease | medical condition referring to damage to the kidney due to chronic high blood pressure |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Functional disorder | medical condition that impairs normal functioning of bodily processes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Disorders of consciousness | medical condition that inhibit consciousness |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Septic shock | medical condition that occurs when sepsis leads to dangerously low blood pressure |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Malnutrition | medical condition that results from eating too little, too much, or the wrong nutrients |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Achilles tendon rupture | medical condition were the tendon at the back of the ankle breaks |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Frostbite | medical condition where localized damage is caused to skin and other tissues due to freezing |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bone disease | medical condition which affects the bone |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sarcopenic obesity | medical condition which is defined as the presence of both sarcopenia and obesity |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Jaundice | medical condition with yellowish pigmentation of the skin or sclerae by bilirubin |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cardiac asthma | medical diagnosis of wheezing, coughing or shortness of breath due to congestive heart failure |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Adrenal crisis | medical emergency |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Esophageal food bolus obstruction | medical emergency caused by the obstruction of the esophagus by an ingested foreign body |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Shock (circulatory) | medical emergency characterized by decreased tissue perfusion and impaired cellular metabolism resulting from failure of circulatory system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Diverticulum | medical or biological term for an outpouching of a hollow (or a fluid-filled) structure in the body |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Complications of pregnancy | medical problems caused by pregnancy in the mother |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tetany | medical sign consisting of the involuntary contraction of muscles |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Achlorhydria | medical state where the production of hydrochloric acid in gastric secretions of the stomach and other digestive organs is absent or low |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Collapse (medical) | medical symptom, a sudden and often unannounced loss of postural tone |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lipohypertrophy | medical term |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bacteriuria | medical term denoting the presence of bacteria in urine |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Obdormition | medical term describing numbness in a limb, often caused by constant pressure on nerves or lack of movement |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hemopneumothorax | medical term describing the combination of two conditions: pneumothorax, or air in the chest cavity, and hemothorax (also called hæmothorax), or blood in the chest cavity |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Acute abdomen | medical term for sudden, severe abdominal pain of unclear origin |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mucosal melanoma | melanoma that has material basis in melanocytes located in mucosal membranes lining the respiratory, gastrointestinal and urogenital tract |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Nodular melanoma | melanoma that is characterized as highly aggressive and manifests as a uniform blue-black, blue-red, or amelanotic nodule |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | False memory | memory of events that actually did not happen |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Repressed memory | memory that is hidden from trauma |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Aseptic meningitis | meningitis caused by anything other than bacteria |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Fungal meningitis | meningitis that has material basis in a fungal infection |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Psychomotor retardation | mental and behavioral disorder involves a slowing-down of thought and a reduction of physical movements in an individual |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Seasonal affective disorder | mental depression that involves presentation of depressive symptoms only during a specific season of the year |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Endogenous depression | mental depression that is characterized by a dysregulation of the endogenous opioid system and not of the monaminergic system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dissociative disorder not otherwise specified | mental disease of brain, cord, body |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Paranoid personality disorder | mental disorder characterized by paranoia and a pervasive, long-standing suspiciousness and generalized mistrust of others |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Excoriation disorder | mental disorder involving compulsive skin-picking |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Substance use disorder | mental disorder involving the abuse or dependence on a substance that is ingested in order to produce a high, alter one's senses, or otherwise affect functioning |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Neurodevelopmental disorder | mental disorder that are impairments of the growth and development of the brain or central nervous system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Posttraumatic stress disorder | mental disorder that developed after experiencing or witnessing a terrifying or life-threatening event |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Arithmomania | mental disorder whereby someone has a strong need to count their actions or nearby objects |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dissociative identity disorder | mental disorder, characterized by multiple personality states and amnesia |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Psychiatric disorders of childbirth | mental disorders developed by the mother related to the delivery process |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Korsakoff syndrome | mental illness caused by a lack of thiamine in the brain |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Inflammatory myofibroblastic tumour | mesenchymal cell neoplasm that has material basis in myofibroblastic cells admixed with inflammatory cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ketoacidosis | metabolic condition |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gilbert's syndrome | metabolic disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypoalphalipoproteinemia | metabolic disorder characterized by deficiency of high density (alpha) lipoprotein in the blood |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Molybdenum cofactor deficiency | metal metabolism disease characterized by encephalopathy that worsens over time resulting from the absence of molybdenum cofactor which leads to accumulation of toxic levels of sulphite and neurological damage |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | HFE hereditary haemochromatosis | metal metabolism disorder characterized by the accumulation of iron in various organs of the body |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Jansen's metaphyseal chondrodysplasia | metaphyseal dysplasia that has material basis in mutation in PTH receptor which results in short-limbed dwarfism |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Metaphyseal chondrodysplasia Schmid type | metaphyseal dysplasia that results in dwarfism and bowed legs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cartilage–hair hypoplasia | metaphyseal dysplasia that results in short-limbed dwarfism and fine sparse hair |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Microscopic polyangiitis | microscopic polyangiitis (MPA) is an inflammatory, necrotizing, systemic vasculitis that affects predominantly small vessels (i.e. small arteries, arterioles, capillaries, venules) in multiple organs. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mastoiditis | middle ear disease characterized by an inflammation of the mucosal lining of the mastoid antrum and the mastoid air cell system inside the mastoid process |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Migralepsy | migraine-triggered epileptic seizures |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Knee effusion | mild knee joint effusion |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Miliaria crystallina | miliaria that is characterized by clear, superficial, noninflammed, subcorneal vesicles that easily rupture when rubbed and is located in the stratum corneum |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Witch's milk | milk secreted from the breasts of some newborn human infants of either sex |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Auditory hallucination | misperceiving mental aural images as if from a physically external sonic source |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Trombiculosis | mite infestation that involves rash caused by Leptotrombidium deliense |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | MERRF syndrome | mitochondrial disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pearson syndrome | mitochondrial metabolism disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Coenzyme Q10 deficiency | mitochondrial metabolism disease that is characterized by a deficiency of CoQ10 resulting from reduced biosynthesis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mohr–Tranebjærg syndrome | mitochondrial metabolism disease that is characterized by hearing loss that begins early in life, problems with movement, impaired vision, and behavior problems |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mitral valve stenosis | mitral valve disease that is characterized by the narrowing of the orifice of the mitral valve of the heart |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mitral valve prolapse | mitral valve disease where one or both of the cusps of the mitral valve bulge or collapse backward in the left atrium during systole |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Carcinosarcoma | mixed cell type cancer that has material basis in carcinomatous (epithelial tissue) and sarcomatous (connective tissue) components |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Vaginal discharge | mixture of liquid, cells, and bacteria, produced in the vagina and cervix, lubricating and protecting the vagina; typically clear or white in color, with consistency varying from thin to thick, typically without a strong odor |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | X-linked recessive inheritance | mode of inheritance |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Binge drinking | modern epithet for drinking alcoholic beverages with an intention of becoming intoxicated by heavy consumption of alcohol over a short period of time |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Aarskog–Scott syndrome | monogenic disease affects a person's height, muscles, skeleton, genitals, and appearance of the face |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Alport syndrome | monogenic disease characterized by glomerulonephritis, endstage kidney disease, and hearing loss |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tietz syndrome | monogenic disease that is characterized by congenital profound bilateral sensorineural hearing loss and generalized albino-like hypopigmentation of skin, eyes and hair that has material basis in mutation in the MITF gene on chromosome 3p13 |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Melancholia | mood disorder of non-specific depression |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dysthymia | mood disorder that involves the presence of a low mood almost daily over a span of at least two years |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypomania | mood state characterized by persistent and pervasive elevated or irritable mood |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Heliophobia | morbid fear of sunlight or excessive sensitivity of the eyes to sunlight |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Urticaria pigmentosa | most common form of cutaneous mastocytosis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Capillary hemangioma | most common variant of hemangioma, dull red, firm, dome-shaped hemangioma, usually located on the head and neck, which grows rapidly caused by proliferation of immature capillary vessels |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Congenital cytomegalovirus infection | mother-to-child transmission of cytomegalovirus occurring in the prenatal period |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Primary lateral sclerosis | motor neuron disease characterized by painless but progressive weakness and stiffness of the muscles of the legs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dysarthria | motor speech disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hairy leukoplakia | mouth disease characterized by a white patch on the lateral sides of the tongue with a corrugated or hairy appearance; caused by Epstein-Barr virus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chorea | movement disease characterized by brief, semi-directed, irregular movements that not repetitive or rhythmic, but appear to flow from one muscle to the next |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Congenital mirror movement disorder | movement disease characterized by involuntary movements of one side of the body that mirror intentional movements on the opposite side primarily involving the upper limbs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Stiff-person syndrome | movement disease that is of unknown etiology characterized by progressive rigidity |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Essential tremor | movement disorder causing involuntary tremors, especially in the hands. It occurs alone without other neurological signs and symptoms. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hyaluronidase deficiency | mucopolysaccharidosis characterized by a deficiency in hyaluronidase |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sly syndrome | mucopolysaccharidosis characterized by a deficiency of the lysosomal enzyme beta-glucuronidase resulting in the inability to degrade glucuronic acid-containing glycosaminoglycans |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hunter syndrome | mucopolysaccharidosis characterized by a deficiency of the lysosomal enzyme iduronate sulfatase |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sanfilippo syndrome | mucopolysaccharidosis characterized by a deficiency of the lysosomal enzyme resulting in incomplete breakdown of the heparan sulfate sugar chain |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Scheie syndrome | mucopolysaccharidosis characterized by corneal clouding, facial dysmorphism and normal lifespan |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Biotinidase deficiency | multiple carboxylase deficiency that involves a deficiency in biotinidase |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Holocarboxylase synthetase deficiency | multiple carboxylase deficiency that involves a deficiency in holocarboxylase synthetase |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Locked twins | multiple pregnancy in which fetuses are interlocked |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cockayne syndrome | multisystem condition characterized by short stature, a characteristic facial appearance, premature aging, photosensitivity, progressive neurological dysfunction, and intellectual deficit |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Vogt–Koyanagi–Harada disease | multisystem disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Wilson's disease | multisystem disease due to abnormal accumulation of copper |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Fasciculation | muscle contraction |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Inflammatory myopathy | muscle disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Atony | muscle losing its strength |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Spasticity | muscle paralysis, increased tendon reflex activity, hypertonia |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Myotonia congenita | muscle tissue disease that is characterised by slow muscle relaxation associated with hyperexcitation of the muscle fibres |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Paratonia | muscular disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Limb-girdle muscular dystrophy | muscular dystrophy characterized by weakening of the muscles of the hip and shoulders which comprise the limb girdle muscles |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Emery–Dreifuss muscular dystrophy | muscular dystrophy that chiefly affects muscles used for movement (skeletal) and heart (cardiac) muscle |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Connective tissue neoplasm | musculoskeletal system cancer that is located in connective tissue |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Myosarcoma | musculoskeletal system cancer that is located in muscle |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Connective tissue disease | musculoskeletal system disease that affects tissues such as skin, tendons, and cartilage |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | White piedra | mycosis that is a superficial fungal infection of the hair shaft caused by Trichosporon beigelii |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chronic myelogenous leukemia | myeloid leukemia that is characterized by over production of white blood cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Acute myeloid leukemia | myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Myelofibrosis | myeloid neoplasm that is located in the bone marrow which results in bone marrow being replaced by fibrous (scar) tissue |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Transient myeloproliferative disease | myeloproliferative neoplasm characterized by leukocytosis in newborns with Down syndrome and rarely in non-Down's infants |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Centronuclear myopathy | myopathy characterized by abnormally located nuclei in skeletal muscle cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Perimyositis | myopathy characterized by inflammation near muscle |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mitochondrial myopathy | myopathy characterized by mitochondrial dysfunction |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Myositis | myopathy characterized by muscle inflammation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Muscular dystrophy | myopathy characterized by progressive skeletal muscle weakness degeneration |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Myoglobinuria | myopathy that is characterized by an increased urinary excretion of myoglobin |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Myositis ossificans | myositis that is accompanied by ossification of muscle tissue or bony deposits in the muscles |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Inclusion body myositis | myositis that is characterized by slowly progressive weakness and wasting of both distal and proximal muscles, most apparent in the muscles of the arms and legs that can occur in a sporadic or hereditary forms |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dermatomyositis | myositis that results in inflammation located in muscle or located in skin where a skin rash is often seen prior to the onset of muscle weakness |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Myxoma | myxoid tumor of primitive connective tissue |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Paronychia | nail disease that is an often-tender bacterial or fungal infection of the hand or foot where the nail and skin meet at the side or the base of a finger or toenail |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Nitrogen narcosis | narcotic effect of high partial pressure respired nitrogen |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hydrogen narcosis | narcotic effect of hydrogen at high partial pressure |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Renal artery stenosis | narrowing of one of the renal arteries, most often caused by atherosclerosis or fibromuscular dysplasia |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Aqueductal stenosis | narrowing of the aqueduct of Sylvius |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Urethral stricture | narrowing of the urethra caused by injury, instrumentation, infection and certain non-infectious forms of urethritis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Carotid artery stenosis | narrowing or constriction of the inner surface (lumen) of the carotid artery, usually caused by atherosclerosis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Stenosing tenosynovitis | narrowing or stenosis of a tendon's retinacular sheath |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Nasal septum perforation | nasal surgery |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Miscarriage | natural death of an embryo or fetus before it is able to survive independently |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Fear of falling | natural fear typical of most humans and mammals |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Substance dependence | need for a drug, whose discontinuation results in withdrawal symptoms |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Alcohol intoxication | negative effect(s) induced by the ingestion of ethanol (alcohol) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Serum sickness | negative reaction against proteins which are contained in a specific serum |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Alogia | negative symptom, restriction in the amount of spontaneous speech |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Transient neonatal diabetes | neonatal diabetes mellitus characterized by hyperglycemia during the neonatal period that remits during infancy but recurs in later life in most patients |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Permanent neonatal diabetes | neonatal diabetes mellitus that has material basis in homozygous mutation in the glucokinase gene (GCK), heterozygous mutation in the KCNJ11 and INS genes, or by heterozygous or homozygous mutation in the ABCC8 gene |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Neonatal hepatitis | neonatal hepatitis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ohtahara syndrome | neonatoal period electroclinical syndrome that is characterized by tonic spasms and partial seizures |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Adrenal tumor | neoplasm (disease) that involves the adrenal gland |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Brain stem tumor | neoplasm (disease) that involves the brainstem |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Nervous system neoplasm | neoplasm (disease) that involves the nervous system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Complex and mixed tumor | neoplasm composed of at least two distinct cellular populations |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Adipose tissue neoplasm | neoplasm derived from adipose tissue |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Onychomatricoma | neoplasm involving a UBERON:0002283 |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Neoplasms of the nailbed | neoplasm involving a nail |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Spinal tumor | neoplasm located in the spinal cord |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Adnexal and skin appendage neoplasms | neoplasms composed of skin appendage tissues |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Glomerulonephritis | nephritis that causes inflammation of the glomeruli located in kidney |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cauda equina syndrome | nerve damage at the end of the spinal cord |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Diabetic neuropathy | nerve damaging disorders associated with diabetes mellitus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Neuroma | nervous system benign neoplasm that is characterized as a nerve tissue tumor |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hyperekplexia | nervous system disease characterized by an exaggerated startle response to sudden, unexpected auditory or tactile stimuli and hypertonia |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Central nervous system disease | nervous system disease that affects either the spinal cord (myelopathy) or brain (encephalopathy) of the central nervous system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Locked-in syndrome | nervous system disease that is characterized by complete paralysis of all voluntary muscles except for the ones that control the movements of the eyes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Neuroleptic malignant syndrome | nervous system disease that is characterized by hyperthermia, muscular rigidity, autonomic dysfunction and altered consciousness and is associated with administration of antipsychotic and other central dopaminergic blockers |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gerstmann syndrome | nervous system disease that results from damage located in left parietal lobe, has symptom agraphia, has symptom acalculia, has symptom finger agnosia |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Toxic encephalopathy | nervous system disease that results from exposure to neurotoxicants and is characterized by an altered mental status, memory loss, and visual problems |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chronic traumatic encephalopathy | neurodegenerative disease caused by repeated head injuries |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tauopathy | neurodegenerative disease caused by tau protein aggregates |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Neurodegeneration with brain iron accumulation | neurodegenerative disease characterized by progressive iron accumulation in the basal ganglia and other regions of the brain, resulting in extrapyramidal movements, such as parkinsonism and dystonia |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Amyotrophic lateral sclerosis | neurodegenerative disease characterized by progressive muscular paralysis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dementia pugilistica | neurodegenerative disease found in people who have had multiple head injuries |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Synucleinopathy | neurodegenerative disease that is characterized by the abnormal accumulation of aggregates of alpha-synuclein protein in neurons, nerve fibres or glial cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Canavan disease | neurodegenerative disorder; its spectrum varies between severe forms with leukodystrophy, macrocephaly and severe developmental delay, and a very rare mild/juvenile form characterized by mild developmental delay |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Williams syndrome | neurodevelopmental disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Megalencephaly | neurodevelopmental disorder characterized by abnormally large brain. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Motor disorder | neurodevelopmental motor disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pulmonary neuroendocrine tumor | neuroendocrine tumor localized to the lung |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gastrinoma | neuroendocrine tumor that results in an overproduction of gastric acid |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Myelopathy | neurologic deficit related to the spinal cord |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pseudobulbar affect | neurologic disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Misophonia | neurologic disorder leading to extremely negative reactions and feelings related to certain sounds |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | High-pressure nervous syndrome | neurological and physiological disorder experienced by divers |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Synesthesia | neurological condition |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dyscalculia | neurological condition, acquired difficulty with performing simple mathematical calculations |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lateral medullary syndrome | neurological disorder causing a range of symptoms due to ischemia in the lateral part of the medulla oblongata in the brainstem |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Motor neuron disease | neurological disorder that selectively affect motor neurons |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Transient ischemic attack | neurological dysfunction by transiently ischemia |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dystonia | neurological movement disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sundowning | neurological phenomenon |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ataxia | neurological sign consisting of lack of voluntary coordination of muscle movements (e.g. gait abnormality, speech changes, abnormalities in eye movements); indicates dysfunction of parts of the nervous system coordinating movement, e.g. cerebellum |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Minamata disease | neurological syndrome caused by severe mercury poisoning |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Developmental disability | neurologically-based disability beginning before adulthood |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Brody myopathy | neuromuscular disease is characterized by difficulty relaxing muscles and muscle stiffness following exercise or other strenuous activity and is located in skeletal muscles |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Charcot–Marie–Tooth disease | neuromuscular disease that is characterized by a slowly progressive degeneration of the muscles of the foot, lower leg, hand and forearm |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Neuromuscular junction disease | neuromuscular disease that is characterized by the disfunction of conduction through the neuromuscular junction |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gray matter heterotopia | neuronal migration disorder characterised by clumps of ectopic neurones in the gray matter |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Trigeminal neuralgia | neuropathic disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hippocampal sclerosis | neuropathological condition with severe neuronal cell loss and gliosis in the hippocampus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Neuromuscular disease | neuropathy that affect the nerves that control the voluntary muscles |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cranial nerve disease | neuropathy that is located in one of the twelve cranial nerves |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Alien hand syndrome | neuropsychiatric disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hemispatial neglect | neuropsychological condition in which, after damage to one hemisphere of the brain is sustained, a deficit in attention to and awareness of one side of space is observed |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hysteria | neurotic disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Weber's syndrome | neurovascular disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Anaplastic large-cell lymphoma | non-Hodgkin lymphoma involving aberrant T-cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | B-cell lymphoma | non-Hodgkin lymphoma that has material basis in B cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | MALT lymphoma | non-Hodgkin lymphoma that has material basis in mucosal tissue involved in antibody production |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Follicular lymphoma | non-Hodgkin lymphoma that is characterized as an indolent non-Hodgkin's lymphoma and has_material_basis_in follicle center B-cells (centrocytes and centroblasts). |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cutaneous T cell lymphoma | non-Hodgkin's lymphoma that has material basis in a mutation of T cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Nonallergic rhinitis | non-allergic rhinitis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Seborrheic keratosis | non-cancerous (benign) skin tumour that originates from cells in the outer layer of the skin |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cavernous liver haemangioma | non-cancerous tumor of the liver |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tietze syndrome | non-cardiac thoracic pain syndrome |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ichthyosis acquisita | non-hereditary form of ichthyosis characterized by plate-like scales on the legs, arms and occasionally the torso |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Nephrosis | non-inflammatory kidney disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Plantar fibromatosis | non-malignant thickening of the feet's deep connective tissue |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sixth nerve palsy | non-neoplastic or neoplastic disorder affecting the abducens nerve (sixth cranial nerve) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Adenocarcinoma of the lung | non-small cell lung carcinoma that derives from epithelial cells of glandular origin |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Grisel's syndrome | non-traumatic subluxation of the atlanto-axial joint caused by inflammation of the adjacent tissues. This is a rare disease that usually affects children. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Benign prostatic hyperplasia | noncancerous increase in size of the prostate |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Osteitis pubis | noninfectious inflammation of the pubis symphysis (also known as the pubic symphysis, symphysis pubis, or symphysis pubica), causing varying degrees of lower abdominal and pelvic pain |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chordoma | notochordal cancer that derives from cellular remnants of the notochord |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Nitrogen deficiency | nutrient deficiency |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Biotin deficiency | nutritional deficiency disease that is characterized by thinning of the hair (often with loss of hair color), and red scaly rash around the eyes, nose, and mouth |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Boron deficiency (medicine) | nutritional disorder in animals |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Boron deficiency (plant disorder) | nutritional disorder in plants |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Parental obesity | obesity of either parent during pregnancy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Compulsive buying disorder | obsession with shopping and buying behavior that causes adverse consequences |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Radiophobia | obsessive fear of ionizing radiation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Graphomania | obsessive impulse to write |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Egomania | obsessive preoccupation with one's self |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ventricular outflow tract obstruction | occlusion of the outflow tract in a ventricle of the hear |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Terson syndrome | occurrence of a vitreous hemorrhage of the human eye |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Night sweats | occurrence of excessive sweating during sleep |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Superior limbic keratoconjunctivitis | ocular disease characterized by episodes of recurrent inflammation of the superior cornea and limbus, as well as of the superior tarsal and bulbar conjunctiva |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ocular larva migrans | ocular form of the larva migrans syndrome that occurs when larvae invade the eye |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Congenital fibrosis of the extraocular muscles | ocular motility disease that is characterized by the inability to move the eyes in certain directions, droopy eyelids and eyes that are fixed in an abnormal position |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cementoma | odontogenic tumor of cementum |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Breakthrough bleeding | of the menstrual period |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pseudohermaphroditism | old clinical term for an organism that is born with primary sex characteristics of one sex but develops the secondary sex characteristics |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Respiratory tract infection | one of any number of infectious diseases involving the respiratory tract |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | MELAS syndrome | one of the family of mitochondrial cytopathies, which also include MERRF, and Leber's hereditary optic neuropathy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tubo-ovarian abscess | one of the late complications of pelvic inflammatory disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Vanishing twin | one of two twins that never fully forms |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Benzodiazepine dependence | one or more of either tolerance, withdrawal symptoms, drug seeking behaviors, such as continued use despite harmful effects, and maladaptive pattern of substance use, according to the DSM-IV |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Geotrichosis | opportunistic mycosis that has material basis in Galactomyces geotrichum, results in systemic infection in immunocompromised people |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Trichosporonosis | opportunistic mycosis that results in disseminated infection, has material basis in Trichosporon and results in formation of nontender erythematous nodules anywhere on the body |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cryptococcosis | opportunistic mycosis that results in fungal infection and has material basis in Cryptococcus neoformans or Cryptococcus gattii. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Microsporidiosis | opportunistic mycosis that results in systemic fungal infection in immunocompromised people, has material basis in Microsporidia phylum members |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chiasmal syndrome | optic nerve disease that is characterized by lesions of the optic chiasm, manifesting as various impairments of the sufferer's visual field according to the location of the lesion along the optic nerve |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Optic neuritis | optic nerve disease that results in inflammation located in optic nerve which may cause a complete or partial loss of vision |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lordosis | or saddle back, curvature of the spine |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Nail biting | oral compulsive habit |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gastrointestinal cancer | organ system cancer located in gastrointestinal tract that is manifested in organs of the gastrointestinal system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Respiratory tract neoplasm | organ system cancer located in the respiratory system that is characterized by uncontrolled cellular proliferation in the respiratory tract |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Head and neck cancer | organ system cancer that arises in the head or neck region (including the nasal cavity, sinuses, lips, mouth, salivary glands, throat, or larynx) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Isovaleric acidemia | organic acidemia that disrupts or prevents normal metabolism of the branched-chain amino acid leucine |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Propionic acidemia | organic acidemia that involes a nonfunctional propionyl CoA carboxylase affecting conversion of aminio acids and fats into sugar for energy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Methylmalonic acidemia | organic acidemia that involves an accumulation of methylmalonic acid in the blood |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | 3-Methylglutaconic aciduria | organic acidemia that is characterized by elevated levels of 3-methylglutaconic acid and 3-methylglutaric acid in the urine |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Post-concussion syndrome | organic brain syndrome that occurs following head trauma (i.e. concussion) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | General paresis of the insane | organic mental disorder caused by late-stage syphilis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Aortic aneurysm | orta to greater than 1.5 times normal size. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Baastrup's sign | orthopedic and radiographic disorder that often occurs in elderly humans |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cantú syndrome | osteochondrodysplasia characterized by congenital hypertrichosis, neonatal macrosomia, and cardiomegaly |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Osteogenesis imperfecta | osteochondrodysplasia that has material basis in a deficiency in type-I collagen which results in brittle bones and defective connective tissue |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Campomelic dysplasia | osteochondrodysplasia that has material basis in a mutation in chromosome 17 which results in bowing in the located in tibia or located in femur |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pycnodysostosis | osteochondrodysplasia that has material basis in a mutation in the CTSK gene which results in dwarfism, brittle bones, osteopetrosis, shortening of the distal phalanges |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Diastrophic dysplasia | osteochondrodysplasia that has material basis in abnormal cartilage development due to mutations in the SLC26A2 gene which results in short limb dwarfism |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Albright's hereditary osteodystrophy | osteochondrodysplasia that has material basis in lack of responsiveness to parathyroid hormone which results in shortening and widening of long bones of the located in hand or located in foot along with short stature, obesity, and rounded face |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Acromesomelic dysplasia | osteochondrodysplasia that has material basis in mesomelia and acromelia, which results in short limb Dwarfism |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypochondroplasia | osteochondrodysplasia that has material basis in mutation in the FGFR3 gene which affects ossification of cartilage and results in short limb dwarfism |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pseudoachondroplasia | osteochondrodysplasia that has material basis in mutations in the COMP gene which results in short limb dwarfism |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cleidocranial dysostosis | osteochondrodysplasia that has material basis in mutations in the RUNX2 gene which results in undeveloped or absent located in clavicle along with delayed closing of fontanels in the located in skull |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Otospondylomegaepiphyseal dysplasia | osteochondrodysplasia that results from mutations in the COL11A2 gene which results in enlargement of the located in epiphysis in located in hand and located in foot, distinct facial features, platyspondyly and hearing loss |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Spondyloepimetaphyseal dysplasia | osteochondrodysplasia that results in abnormalities of bone growth located in vertebral column, located in epiphysis, located in metaphysis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Achondroplasia | osteochondrodysplasia that results in dwarfism from abnormal ossification of cartilage in long bones |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Blount's disease | osteochondrodysplasia that results in inward turning of lower leg, located in tibia, which fails to develop normally |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Thanatophoric dysplasia | osteochondrodysplasia that results in short arms and legs with excess folds of skin |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Weissenbacher–Zweymüller syndrome | osteochondrodysplasia that results in shortened long bones and distinct facial abnormalities |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Metaphyseal dysplasia | osteochondrodysplasia that results in thinning and the tendency to fracture located in bone |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Osgood–Schlatter disease | osteochondrosis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Scheuermann's disease | osteochondrosis that results in abnormal bone growth and curvature located in thoracic vertebral column |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Köhler disease | osteochondrosis that results in death and collapse located in navicular bone of foot |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Legg–Calvé–Perthes disease | osteochondrosis that results in death and fracture located in hip joint |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cole-Carpenter syndrome | osteogenesis imperfecta characterized by craniosynostosis, communicating hydrocephalus, ocular proptosis, marked postnatal growth failure, and distinctive facial appearance |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chronic recurrent multifocal osteomyelitis | osteomyelitis characterized by multiple foci of painful swelling of bones, mainly in the metaphyses of the long bones, in addition to the pelvis, the shoulder girdle and the spine |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Juvenile osteoporosis | osteoporosis with no known cause that is characterized by pain in the back and extremities, walking difficulties, multiple fractures, and radiological evidence of osteoporosis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Melorheostosis | osteosclerosis that has material basis in a mutation of the LEMD3 gene which results in a hyperdense bony cortex |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Craniometaphyseal dysplasia | osteosclerosis that has material basis in mutations in the ANKH gene which results in progressive thickening located in skull and abnormally shaped ends of long bones in the limbs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Axial osteomalacia | osteosclerosis that results in coarsening located in trabecular bone |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Craniodiaphyseal dysplasia | osteosclerosis that results in increased calcium concentration located in skull which decreases the size of cranium foramina and cervical spinal canal |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Osteopoikilosis | osteosclerosis that results in numerous bone islands located in skeleton |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Otosclerosis | otitis interna characterized by an abnormal bone growth in the middle ear |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Labyrinthitis | otitis interna which involves inflammation of the labyrinths |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Otitis media | otitis which involves inflammation of the middle ear |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gay bowel syndrome | outdated medical term |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Luteoma | ovarian benign neoplasm characterized by solid proliferations of luteinized cells, resulting in a tumor-like ovarian enlargement that regresses during the puerperium |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Clear-cell ovarian carcinoma | ovarian carcinoma that has material basis in cells with clear cytoplasm and glycogen secreting hob nail cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Corpus luteum cyst | ovarian cyst that may rupture during menstruation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Premature ovarian failure | ovarian disease where ovaries do not produce estrogen despite high levels of circulating gonadotropins in women under 40 |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Surface epithelial-stromal tumor | ovarian tumor that is derived_from ovarian surface epithelium |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ovarian serous cystadenoma | ovary serous adenoma that has material basis in glandular epithelium, in which cystic accumulations of retained secretions are formed |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cholinergic crisis | over-stimulation at a neuromuscular junction due to an excess of acetylcholine |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Epiphora (medicine) | overflow of tears onto the face |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypopnea | overly shallow breathing or an abnormally low respiratory rate |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tertiary hyperparathyroidism | overproduction of parathyroid hormone that is autonomous and often associated with chronic secondary hyperparathyroidism |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Vitamin B6 deficiency | paediatric disease due to a lack of pyridoxine |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dysmenorrhea | pain during menstruation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Coccydynia | pain in the coccyx or tailbone area |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ear pain | pain in the ear |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Herpetic whitlow | painful blister of the periungual skin that is caused by herpes simplex virus type 1 or 2 |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cracked nipple | painful, postpartum condition in breastfeeding women |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Amaurosis fugax | painless temporary loss of vision in one or both eyes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pallor | pale skin |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sister Mary Joseph nodule | palpable nodule bulging into the umbilicus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Annular pancreas | pancreas disease characterized by autosomal dominant inheritance of the annular pancreas (head of the pancreas forming a ring around the second portion of the duodenum) and duodenal stenosis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Homosexual panic | panic due to the pressure of uncontrollable perverse sexual cravings |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Erythema induratum | panniculitis on the calves. It occurs mainly in women, but it is very rare now |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tetraplegia | paralysis of all four limbs and torso |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hemiplegia | paralysis of the arm, leg, and trunk on the same side of the body |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cycloplegia | paralysis of the ciliary muscle of the eye, resulting in a loss of accommodation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Paraneoplastic cerebellar degeneration | paraneoplastic syndrome that involves the nervous system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pedophilia | paraphilia characterized by a sexual attraction to prepubescent children |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pyrophilia | paraphilia in which a subject derives gratification from fire and fire-starting activity |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sexual sadism disorder | paraphilia in which a subject derives gratification from giving pain |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Masochism | paraphilia in which a subject derives gratification from receiving pain |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Kleptolagnia | paraphilia in which a subject derives gratification from stealing |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dendrophilia (paraphilia) | paraphilia in which people are sexually attracted to or sexually aroused by trees |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Symphorophilia | paraphilia in which sexual arousal involves staging and watching a tragedy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Biastophilia | paraphilia in which sexual arousal is dependent on, or is responsive to, the act of assaulting an unconsenting person |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Urolagnia | paraphilia in which sexual excitement is associated with urine or urination |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Zoophilia | paraphilia involving a sexual fixation on non-human animal |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Frotteurism | paraphilic interest in rubbing |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Filariasis | parasitic disease caused by a family of nematode worms |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Protozoan infection | parasitic disease caused by a protozoan |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ectoparasitic infestation | parasitic disease caused by organisms that live primarily on the surface of the host |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Taeniasis | parasitic disease due to infection with tapeworms belonging to the genus Taenia |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Trichinosis | parasitic disease due to invasion by Trichinella spp. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Giardiasis | parasitic disease of humans and other mammals |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Echinococcosis | parasitic disease of tapeworms of the Echinococcus type |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pediculosis | parasitic ectoparasitic infectious disease that involves infestation of lice, which are blood-feeding ectoparasitic insects of the order Phthiraptera |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Acariasis | parasitic ectoparasitic infectious disease that involves infestation of mites belonging to the family Sarcoptidae, Trombiculidae and Demodicidae |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Myiasis | parasitic ectoparasitic infectious disease that is caused by parasitic dipterous fly larvae (maggots) feeding on the host's necrotic or living tissue |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Angiostrongyliasis | parasitic helminthiasis infectious disease that involves parasitic infection of the intestine, central nervous system and eyes by Angiostrongylus cantonensis or Angiostrongylus costaricensis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Toxoplasmosis | parasitic human disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Trypanosomiasis | parasitic protozoa infectious disease that involves infection caused by parasitic protozoan of the genus Trypanosoma in animals and humans |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | East Coast fever | parasitic protozoa infectious disease that involves infection of humans and cattle caused by a genus of parasitic protozoa Theileria, which is transmitted by ixodid ticks |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Fasciolosis | parasitic worm infection caused by the common liver fluke Fasciola hepatica as well as by Fasciola gigantica |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Parotitis | parotid disease characterized by the inflammation of one or both parotid glands |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Prodrome | part of disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Coronary occlusion | partial or complete obstruction of blood flow in a coronary artery |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Trisomy 16 | partial or complete triplication of chromosome 16 |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Trisomy 22 | partial or complete triplication of chromosome 22 |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Trisomy 9 | partial or complete triplication of chromosome 9 |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Atrophy | partial or complete wasting away of a part of the body |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hearing loss | partial or total inability to hear |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Armpit fetishism | partialism in which an individual is sexually attracted to armpits |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Char syndrome | patent ductus arteriosus with facial dysmorphism and abnormal fifth digits |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lymphangiectasia | pathologic dilation of lymph vessels |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Complicated grief disorder | pathological (and lasting) reaction to loss |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cinchonism | pathological condition caused by an overdose of quinine or quinidine |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Poisoning | pathological condition caused by exposure, ingestion, injection or inhalation of a toxic substance |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Maculopathy | pathological condition of the macula in the eye |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sequela | pathological condition resulting from a disease, injury, therapy, or other trauma |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Trypophobia | pathological fear |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mysophobia | pathological fear of contamination and germs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ablutophobia | pathological fear of washing or bathing |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Disseminated intravascular coagulation | pathological process characterized by the widespread activation of the clotting cascade that results in the formation of blood clots in the small blood vessels throughout the body |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Thrombotic microangiopathy | pathology that results in thrombosis in capillaries and arterioles, due to an endothelial injury |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mesial temporal sclerosis | pattern of hippocampal neuron cell loss |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hospitalism | pediatric diagnosis used in the 1930s to describe infants who wasted away while in hospital |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Disease mongering | pejorative term for the practice of widening the diagnostic boundaries of illnesses and aggressively promoting their public awareness in order to expand the markets for treatment |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Muselmann | people who follow or practice Islam |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lymphedema–distichiasis syndrome | people with this hereditary condition have a double row of eyelashes, |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Palpitations | perceived abnormality of the heartbeat |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hallucination | perception in the absence of external stimulation that has the qualities of real perception |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Phantom limb | perception of painful and nonpainful phantom sensations that occur following the complete or partial loss of a limb |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tinnitus | perception of sound within the human ear ("ringing of the ears") when no external sound is present |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Phantom vibration syndrome | perception that one's mobile phone is vibrating or ringing when it isn't |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Aura (symptom) | perceptual disturbance experienced by some migraine sufferers |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gastrointestinal perforation | perforation in the wall of part of the gastrointestinal tract. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Compulsive behavior | performing an act persistently and repetitively without it necessarily leading to an actual reward or pleasure |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hemopericardium | pericardial effusion that results from blood in the pericardial sac |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dressler syndrome | pericarditis characterized by inflammation, occurring after injury, located in pericardium |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pericardial effusion | pericardium disease that is characterized by an abnormal accumulation of fluid in the pericardial cavity |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pericarditis | pericardium disease that is characterized by an inflammation of the pericardium and has symptom chest pain |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Panic attack | period of intense fear or apprehension of sudden onset |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Brief psychotic disorder | period of psychosis whose duration is generally shorter, is not always non-recurring, but can be, and is not caused by another condition |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Adams–Stokes syndrome | periodic fainting spell in which there is a periodic onset and offset of blockage of heart due to disorder of heart rhythm |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Aggressive periodontitis | periodontitis that is characterized by rapid attachment loss and bone destruction in the presence of little local factors such as dental plaque and dental calculus resulting in inflammation and a loss of periodontium |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Angioimmunoblastic T-cell lymphoma | peripheral T-cell lymphoma characterized by autoimmune features and poor prognosis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Nerve sheath tumor | peripheral nervous system neoplasm that is located in the connective tissue surrounding nerves |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hereditary neuropathy with liability to pressure palsy | peripheral neuropathy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Polyneuropathy | peripheral system disease that is characterized by damage affecting peripheral nerves (peripheral neuropathy) in roughly the same areas on both sides of the body, featuring weakness, numbness, pins-and-needles, and burning pain |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Priapism | peripheral vascular disease characterized by blood trapped in the penis that is unable to drain. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Peritoneal mesothelioma | peritoneum cancer that develops from cells of the mesothelium and is located in the peritoneum |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Nonunion | permanent failure of healing following a broken bone |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pseudarthrosis | permanent failure of healing following a broken bone unless intervention (such as surgery) is performed |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Volkmann's contracture | permanent flexion contracture of the hand at the wrist, resulting in a claw-like deformity of the hand and fingers |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Aquaphobia | persistent and abnormal fear of water |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Globus pharyngis | persistent but painless sensation of having a pill, food bolus, or some other sort of obstruction in the throat when there is none |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cyclothymia | persistent instability of mood that involves recurrent hypomanic and dysthymic episodes, but no full manic episodes or full major depressive episodes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Female sexual arousal disorder | persistent or recurrent inability to attain sexual arousal or to maintain arousal until the completion of a sexual activity |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Perseveration | persistent repetition of previously used phrases, words or details (psychopathological symptom) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Idiot | person of low intelligence |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | High-functioning alcoholic | person who maintains jobs and relationships while exibiting alcoholism |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Obsessive–compulsive personality disorder | personal perfectionism at the cost of flexibility, openness, efficiency & affect on others |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Geschwind syndrome | personality changes associated with epilepsy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Schizoid personality disorder | personality disorder characterized by a lack of interest in social relationships, a tendency towards a solitary or sheltered lifestyle, secretiveness, emotional coldness, and apathy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Histrionic personality disorder | personality disorder characterized by excessive emotionality and attention-seeking |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Borderline personality disorder | personality disorder characterized by variability of moods and unstable relationships |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sadistic personality disorder | personality disorder diagnosis involving sadism |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Schizotypal personality disorder | personality disorder that involves a need for social isolation, anxiety in social situations, odd behavior and thinking, and often unconventional beliefs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Narcissistic personality disorder | personality disorder that involves an excessive preoccupation with issues of personal adequacy, power, prestige and vanity |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Avoidant personality disorder | personality disorder that is characterized by a pervasive pattern of social inhibition, feelings of inadequacy, extreme sensitivity to negative evaluation, and avoidance of social interaction |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dependent personality disorder | personality disorder that is characterized by a pervasive psychological dependence on other people |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sensory processing sensitivity | personality trait |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Drug tolerance | pharmacological concept describing subjects' reduced reaction to a drug following its repeated use |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Oropharyngeal cancer | pharynx cancer that is located in the oropharynx |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypopharyngeal cancer | pharynx cancer that is located in the hypopharynx |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sleepwalking | phenomenon of combined sleep and wakefulness |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | List of mass hysteria cases | phenomenon that transmits collective illusions of threats, whether real or imaginary, through a population in society as a result of rumors and fear |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Thrombophlebitis | phlebitis that results from a blood clot in the vessel |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gymnophobia | phobia for naked bodies |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Fear of frogs | phobia known as frog phobia or ranidaphobia |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Fear of flying | phobia of flying |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Acrophobia | phobia specific to heights |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Fear of crossing streets | phobia that affects a person's ability to cross a street or roadway |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Agoraphobia | phobic disorder involving the specific anxiety about being in a place or situation where escape is difficult or embarrassing or where help may be unavailable. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Social anxiety disorder | phobic disorder that involves social anxiety |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Specific phobia | phobic disorder that is characterized by an unreasonable or irrational fear related to exposure to specific objects or situations |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Photodermatosis | photoszematose |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Haemolacria | physical condition that causes a person to produce tears that are partially composed of blood |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Omphalocele | physical disorder characterized by a defect in the development of the abdominal wall muscles, resulting in the intestines, liver and other organs to remain outside of the abdomen in a sac |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Renal-hepatic-pancreatic dysplasia | physical disorder characterized by pancreatic fibrosis, renal dysplasia and hepatic dysgenesis; it is usual fatal soon after birth |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Klippel–Feil syndrome | physical disorder that has material basis in abnormal segmentation of the vertebra during fetal development which results in fusion located in cervical vertebra |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ictal | physiologic state or event such as a seizure, stroke, or headache |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Test anxiety | physiological condition |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Jet lag | physiological condition caused by travel across time zones |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bitter pit | physiological disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Diving disorders | physiological disorder resulting from underwater diving |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sterility (physiology) | physiological inability to effect sexual reproduction in a living thing, members of whose kind have been produced sexually |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Olive quick decline syndrome | phytopathology targeting olive trees and causing leaf scorch and death of branches and of the entire plant |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Rope worms | pieces of intestinal lining mistaken for parasites (created using bleach enemas) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Inclusion body rhinitis | pig disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Neonatal jaundice | pigmentation disease characterized by a high level of bilirubin in the blood, causing a yellowing of the skin and other tissues of a newborn infant |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Reticular pigmented anomaly of the flexures | pigmentation disease characterized by a reticulate pattern of abnormally dark skin coloring, particularly in the body's folds and creases |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dyschromatosis symmetrica hereditaria | pigmentation disease characterized by progressively pigmented and depigmented macules, often mixed in a reticulate pattern, concentrated on the dorsal extremities |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dyschromatosis universalis hereditaria | pigmentation disease characterized by reticulate hyper- and hypo-pigmentated macules in a generalized distribution |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pinealoblastoma | pineal gland neoplasm located in the brain |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Remitting seronegative symmetrical synovitis with pitting edema | pitting edema |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypopituitarism | pituitary gland disease characterized by the decreased secretion of one or more of the eight hormones normally produced by the pituitary gland |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chorioamnionitis | placenta disease that is an inflammation of the fetal membranes (amnion and chorion) due to a bacterial infection |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Oligohydramnios | placenta disease that is characterized by a deficiency of amniotic fluid sometimes resulting in an embryonic defect through adherence between embryo and amnion |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Placenta accreta | placenta disease that is characterized by an abnormally deep attachment of the placenta, through the endometrium and into the myometrium |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Polyhydramnios | placenta disease that is characterized by an excess of amniotic fluid in the amniotic sac |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Placental insufficiency | placenta disease that is characterized by insufficient blood flow to the placenta during pregnancy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Placenta praevia | placenta disease that is characterized by placenta attachment to the uterine wall close to or covering the cervix |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Placental abruption | placenta disease that is characterized by separation of the placental lining from the uterus of the mother |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pneumonic plague | plague that results in infection located in lung, which results from direct inhalation of the bacillus and has symptom fever, has symptom chills, has symptom cough and has symptom difficulty breathing |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dutch elm disease | plant disease caused by Ophiostoma ulmi fungus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Leaf rust (barley) | plant disease caused by fungi of the species Puccinia hordei |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Panama disease | plant disease that primarily effects Bananas |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Calcium deficiency (plant disorder) | plant disorder that can be caused by insufficient calcium in the growing medium, but is more frequently a product of low transpiration of the whole plant or more commonly the affected tissue |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Verticillium wilt | plant wilt disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Plasmacytoma | plasma cell dyscrasia in which a plasma cell tumour grows within soft tissue or within the axial skeleton |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Neonatal alloimmune thrombocytopenia | platelet-related disease affecting fetuses and infants, which can be fatal |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pleurisy | pleural disease that is characterized by swelling, due to inflammation of the pleura, the lining of the pleural cavity surrounding the lung or lungs. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hydrothorax | pleural effusion containing serous liquid |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pneumoperitoneum | pneumatosis (abnormal presence of air or other gas) in the peritoneal cavity, a potential space within the abdominal cavity. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pneumatosis intestinalis | pneumatosis of an intestine, that is, gas cysts in the bowel wall |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Asbestosis | pneumoconiosis caused by inhalation and retention of asbestos fibers |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Berylliosis | pneumoconiosis that involves allergic response located in lungs caused by inhalation of beryllium compounds |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Silicosis | pneumoconiosis that is an inflammation and scarring of the upper lobes of the lungs causing nodular lesions resulting from inhalation of silica, quartz or slate particles |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Caplan's syndrome | pneumoconiosis that results in humans that also have rheumatoid arthritis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pleuropneumonia | pneumonia accompanied by inflammation of the pleura and accumulation of pus in the pleural space caused by bacteria |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pneumocystis pneumonia | pneumonia caused by Pneumocystis jirovecii, common among AIDS patients |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Viral pneumonia | pneumonia described as an inflammatory illness of the lung commonly caused by viruses such as influenza virus, parainfluenza, adenovirus, rhinovirus, herpes simplex virus, respiratory syncytial virus, hantavirus, and cytomegalovirus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bacterial pneumonia | pneumonia involving inflammation of the lungs caused by bacteria |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Idiopathic interstitial pneumonia | pneumonia located in the lung parenchyma of unknown cause |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lead poisoning | poisoning by lead in the body, especially affects the brain |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mercury poisoning | poisoning caused by mercury chemicals |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pesticide poisoning | poisoning of humans from pesticide exposure |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Colorectal polyp | polyp that involves the colon |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gallbladder polyp | polyp that involves the gall bladder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Nasal polyp | polypoidal masses |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Van Gogh syndrome | polysurgical addiction |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Intrauterine growth restriction | poor growth of fetus in mother's womb during pregnancy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Aminolevulinic acid dehydratase deficiency porphyria | porphyria that has symptom abdominal pain, has symptom neuropathy, has symptom autonomic instability and has symptom psychosis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pelvic organ prolapse | portion of the vaginal canal protruding from the opening of the vagina |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Postherpetic neuralgia | post herpétique |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Rheumatic fever | post-streptococcal inflammatory disease that can involve the heart, joints, skin, & brain |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Enophthalmos | posterior displacement of the eyeball within the orbit due to changes in the volume of the orbit (bone) relative to its contents |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cytokine storm | potentially fatal immune reaction |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Diabetic ketoacidosis | potentially life-threatening complication in people with diabetes mellitus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Status dystonicus | potentially life-threatening disorder in people with primary or secondary dystonia |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Transvestism | practice of dressing in a manner traditionally associated with the opposite sex |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bestiality | practice of sexual activity between humans and non-human animals |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Impaired glucose tolerance | pre-diabetic state of hyperglycemia that is associated with insulin resistance and increased risk of cardiovascular pathology. IGT may precede type 2 diabetes mellitus by many years |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Eclampsia | pre-eclampsia characterized by the presence of seizures |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hyperlexia | precocious ability to read words without prior training in learning to read typically before the age of 5 |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Atopy | predisposition towards allergy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Scaphocephaly | premature fusion of the sagittal suture |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Carotenosis | presence in blood of the orange pigment carotene |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Unibrow | presence of abundant hair between the eyebrows |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cerebral venous sinus thrombosis | presence of acute thrombosis (a blood clot) in the dural venous sinuses, which drain blood from the brain. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Traumatic pneumorrhachis | presence of air or gas within the spinal canal cavity |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Proteinuria | presence of an excess of serum proteins in the urine |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bacteremia | presence of bacteria in the blood |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hematospermia | presence of blood in ejaculation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hydropneumothorax | presence of both air and fluid within the pleural space |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Wernicke encephalopathy | presence of neurological symptoms caused by biochemical lesions of the central nervous system after exhaustion of B-vitamin reserves, |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tularemia | primary bacterial infectious disease that has material basis in Francisella tularensis, which is transmitted by dog tick bite (Dermacentor variabilis), transmitted by deer flies (Chrysops sp) or transmitted by contact with infected animal tissues. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chancroid | primary bacterial infectious disease that is a sexually transmitted infection located_in skin of the genitals, has_material_basis_in Haemophilus ducreyi, which is transmitted_by sexual contact. The infection has_symptom painful and soft ulcers. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bartonellosis | primary bacterial infectious disease that is caused by the bacteria of the genus Bartonella |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Relapsing fever | primary bacterial infectious disease that results in infection, has material basis in Borrelia, which is transmitted by tick or transmitted by body louse |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Smoke inhalation | primary cause of death for victims of fires |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Primary ciliary dyskinesia | primary ciliary dyskinesia that is characterized by sinusitis, bronchiectasis and situs inversus with dextrocardia resulting from dysfunction of the cilia during embryologic development |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hyper IgM syndrome | primary immune deficiency disorders characterized by defective CD40 signaling |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lymphoproliferative disorders | primary immunodeficiency disease characterized by immune dysregulation typically after viral infection, usually associated with Epstein-Barr viral infection |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Familial cold urticaria | primary immunodeficiency disease characterized by recurrent episodes of maculopapular skin rash triggered by exposure to cold associated with low-grade fever, general malaise, eye redness and arthralgia/myalgia |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Combined immunodeficiencies | primary immunodeficiency disease that involves multiple components of the immune system, including both humoral immunity and cell-mediated immunity |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Complement deficiency | primary immunodeficiency disease that is the result in a mutation of a gene encoding one of the thirty complement system proteins, produced predominantly in liver, which function to defend against infection and produce inflammation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Phagocyte bactericidal dysfunction | primary immunodeficiency disease where phagocytes have a diminished ability to fight bacterial infection |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Vulvar cancer | primary or metastatic malignant neoplasm involving the vulva |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gonadotropin-resistant ovary syndrome | primary or secondary amenorrhea and is resistant to exogenous gonadotropin stimulation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Blastomycosis | primary systemic mycosis that results in a systemic fungal infection, has material basis in Blastomyces dermatitidis, transmitted by airborne spores and has symptom skin lesions, has symptom lung lesions and has symptom pleural thickening |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sporotrichosis | primary systemic mycosis that results in a systemic fungal infection, has material basis in Sporothrix schenckii in animals and humans and results in formation of red papule at the site of inoculation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Paracoccidioidomycosis | primary systemic mycosis that results in systemic fungal infection located in mucosa, located in lymph nodes, located in bone, located in skin or located in lungs, has material basis in Paracoccidioides brasiliensis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Immune thrombocytopenic purpura | primary thrombocytopenia that involves relatively few platelets in blood as a result of autoantibodies |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | P′′ | primitive computer programming language |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gerstmann–Sträussler–Scheinker syndrome | prion disease characterized by adult onset of memory loss, dementia, ataxia, and pathologic deposition of amyloid-like plaques in the brain |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Stroke | problem of the arteries supplying blood to the brain |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Rh disease | problem with Rh+ fetuses in Rh- mothers |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Near-sightedness | problem with distance vision |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Trifascicular block | problem with the electrical conduction of the heart |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Exsanguination | process of blood loss, to a degree sufficient to cause death |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Carcinogenesis | process of formation of cancer |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bletting | process of softening that certain fleshy fruits undergo, beyond ripening |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Nicotine withdrawal | process of withdrawing from nicotine addiction |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bronchorrhea | production of more than 100 mL per day of watery sputum |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Primary progressive aphasia | progressive language and speech disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chronic kidney disease | progressive loss in kidney function over a period of months or years |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Semantic dementia | progressive neurodegenerative disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Alzheimer's disease | progressive, neurodegenerative disease characterized by memory loss |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Myotonia | prolonged contraction of muscles |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Foot fetishism | pronounced sexual interest in feet |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sexual addiction | proposed compulsive sexual disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Posttraumatic embitterment disorder | proposed disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Irlen syndrome | proposed disorder of vision |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Besnoitiosis | protozoan disease of the skin, subcutis, blood vessels, mucous membranes, and other tissues of animals |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Femoral hernia | protrusion of a viscus through a weakness in the containing wall |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Prolapse | protrusion of an organ in into a natural or artificial orifice |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lung hernia | protrusion of lung outside of thoracic wall |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Zahn infarct | pseudo-infarction of the liver |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cutaneous lymphoid hyperplasia | pseudolymphoma of the skin |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Wind turbine syndrome | pseudomedical diagnosis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gender dysphoria | psychiatric classification of the discordance between gender identity and one's biological sex at birth |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Transvestic fetishism | psychiatric diagnosis applied to those who are thought to have an excessive sexual or erotic interest in cross-dressing |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gender dysphoria in children | psychiatric disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Capgras delusion | psychiatric disorder (syndrome) in which a person holds a delusion that a family member has been replaced by an identical impostor |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Codependency | psychological condition |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Berserk llama syndrome | psychological condition suffered by human-raised llamas and alpacas |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Fragmentation of memory | psychological disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Smile mask syndrome | psychological disorder proposed by professor Makoto Natsume |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Equinophobia | psychological fear of horses |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Self-disorder | psychological phenomenon of disruption or diminishing of a person's sense of minimal (or basic) self |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ataque de nervios | psychological syndrome |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Grandiose delusions | psychopathological condition (that is, when an individual believes that he has exceptional abilities, fame, wealth, or omnipotence) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Kandinsky–Clérambault syndrome | psychopathological syndrome (constellation of symptoms), occurring in schizophrenia |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Catatonia | psychopathological syndrome, a group of postural and movement abnormalities |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Neurasthenia | psychopathological term to denote a condition with symptoms of fatigue, anxiety, headache, heart palpitations, high blood pressure, neuralgia, and depressed mood. also known as effort syndrome |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Brief reactive psychosis | psychosis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Supersensitivity psychosis | psychosis induced by chronic treatment with neuroleptics |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Stendhal syndrome | psychosomatic disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Schizophrenia | psychotic disorder characterized by emotional responsiveness and disintegration of thought processes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Schizophreniform disorder | psychotic disorder that involves schizophrenia symptoms over time period of one month |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Schizoaffective disorder | psychotic disorder that is characterized by recurring episodes of mood fluctuations and a loss of contact with reality |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pleuropulmonary blastoma | pulmonary blastoma that derives from the lung or pleural cavity |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Acute motor axonal neuropathy | pure motor axonal form of Guillain-Barré syndrome |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Xanthinuria | purine-pyrimidine metabolic disorder characterized by deficiency of xanthine oxidase, resulting in excretion of large amounts of xanthine in the urine and the formation of xanthine stones |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dihydropyrimidine dehydrogenase deficiency | purine-pyrimidine metabolic disorder that is an autosomal recessive metabolic disorder in which there is absent or significantly decreased activity of dihydropyrimidine dehydrogenase, an enzyme involved in the metabolism of uracil and thymine |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Havana syndrome | purported acoustic attacks on US embassy staff |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cutaneous diphtheria infection | pyoderma that is a milder form of diphtheria restricted to the skin producing shallow skin ulcers is caused by direct physical contact of individuals infected with Corynebacterium diphtheriae as the bacteria releases the diphtheria toxin |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Orotic aciduria | pyrimidine metabolic disorder that is characterized by an excessive secretion of orotic acid in urine |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dysosmia | qualitative alteration or distortion of the perception of smell |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Myxomatosis | rabbit disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Progeroid syndromes | range of genetic disorders which cause a person to appear to grow older faster |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Whiplash (medicine) | range of injuries to the neck related to a sudden distortion of the neck |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Acute liver failure | rapid deterioration of liver function causing encephalopathy and coagulopathy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Delirium tremens | rapid onset of confusion caused by alcohol withdrawal; usually lasts for 2–3 days; symptoms include nightmare, agitation, global confusion, disorientation, hallucination, fever, high blood pressure, heavy sweating |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Acute basophilic leukemia | rare acute myeloid leukemia in which the immature cells differentiate towards basophils |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ganglioneuroma | rare and benign tumor of the autonomic nerve fibers arising from neural crest sympathogonia |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Paroxysmal tonic upgaze | rare and distinctive neuro-ophthalmological syndrome characterized by episodes of sustained upward deviation of the eyes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Merkel-cell carcinoma | rare and highly aggressive skin cancer |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Epidermolytic hyperkeratosis | rare and severe form of ichthyosis this skin disease affects around 1 in 300,000 people |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mixed autoimmune hemolytic anemia | rare autoimmune disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Noonan syndrome with multiple lentigines | rare autosomal dominant,[3] multisystem disease caused by a mutation in the protein tyrosine phosphatase, non-receptor type 11 gene (PTPN11) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Laurence–Moon syndrome | rare autosomal recessive genetic disorder associated with retinitis pigmentosa, spastic paraplegia, and mental disabilities |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Familial isolated vitamin E deficiency | rare autosomal recessive neurodegenerative disease. Symptoms are similar to those of Friedreich ataxia |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Abderhalden–Kaufmann–Lignac syndrome | rare autosomal-recessive, lysomal storage childhood disorder involving deposits of cystine crystals in various parts of the body, including the bone marrow, conjunctiva and cornea |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Synovial chondromatosis | rare benign chronic progressive metaplasia in which cartilage is formed in synovial membranes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Myelolipoma | rare benign tumor of the adrenal gland |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Schizencephaly | rare birth defect characterized by abnormal clefts lined with grey matter that form the ependyma of the cerebral ventricles to the pia mater. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hh blood group | rare blood type |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Esthesioneuroblastoma | rare cancer of the nasal cavity |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Renal cortical necrosis | rare cause of acute kidney failure |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tetrasomy X | rare chromosomal disorder with 4 X chromosomes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cytochrome b5 deficiency | rare condition and form of isolated 17,20-lyase deficiency caused by deficiency in cytochrome b5 |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Adiposis dolorosa | rare condition characterized by generalized obesity and fatty tumors in the adipose tissue. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hereditary gingival fibromatosis | rare condition of gingival overgrowth |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pelvic digit | rare congenital abnormality in humans |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Long QT syndrome | rare congenital and inherited or acquired heart condition in which delayed repolarization of the heart following a heartbeat increases the risk of episodes of torsades de pointes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gray platelet syndrome | rare congenital autosomal recessive bleeding disorder caused by a reduction or absence of alpha-granules in blood platelets |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | XX male syndrome | rare congenital condition where an individual with a female genotype has phenotypically male characteristics that can vary between cases |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dextrocardia | rare congenital defect in which the apex of the heart is located on the right side of the body |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Diprosopus | rare congenital disorder whereby parts (accessories) or all of the face are duplicated on the head |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Spinal muscular atrophy | rare congenital neuromuscular disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chronic atrophic rhinitis | rare disease of the nasal mucosa |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cerebellar hypoplasia | rare disorder in which the cerebellum is either missing entirely or is smaller than usual |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ganser syndrome | rare dissociative disorder previously classified as a factitious disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | VIPoma | rare endocrine tumor that overproduces vasoactive intestinal peptide |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Protein poisoning | rare form of acute malnutrition thought to be caused by a near complete absence of fat in the diet |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Acute erythroid leukemia | rare form of acute myeloid leukemia (less than 5% of AML cases) where the myeloproliferation is of erythroblastic precursors. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Struma ovarii | rare form of monodermal teratoma that contains mostly thyroid tissue, which may cause hyperthyroidism |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Iniencephaly | rare form of neural tube defect in which a malformation of the cervico-occipital junction is associated with a malformation of the central nervous system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Fatal insomnia | rare form of prion disease characterized by subacute onset of insomnia showing as a reduced overall sleep time, autonomic dysfunction, and motor disturbances |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Adducted thumb syndrome | rare genetic disease affecting palate, thumbs, and upper limbs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mowat–Wilson syndrome | rare genetic disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Alström syndrome | rare genetic disorder caused by mutations in the gene ALMS1 |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Adermatoglyphia | rare genetic disorder causing lack of fingerprints |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pitt–Hopkins syndrome | rare genetic disorder characterized by developmental delay, epilepsy, distinctive facial features, and possible intermittent hyperventilation followed by apnea |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bloom syndrome | rare genetic disorder with short strature and predisposition to cancer |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | WAGR syndrome | rare genetic syndrome in which affected children are predisposed to develop Wilms tumour |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Protein C deficiency | rare genetic trait that predisposes to thrombotic disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pachyonychia congenita | rare group of autosomal dominant skin disorders that are caused by a mutation in one of five different keratin genes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pemphigus | rare group of blistering autoimmune diseases that affect the skin and mucous membranes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Polymyositis | rare idiopathic inflammatory myopathy characterized by symmetric proximal muscle weakness and elevated muscle enzymes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Behçet's disease | rare immune-mediated small-vessel systemic vasculitis in humans |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bickerstaff brainstem encephalitis | rare inflammatory brain disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tangier disease | rare inherited disorder characterized by a severe reduction in the amount of high density lipoprotein (HDL), often referred to as "good cholesterol", in the bloodstream |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Subacute sclerosing panencephalitis | rare insidious sequela from measles infection |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mast cell leukemia | rare leukemia (blood cancer) involving mast cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Alveolar capillary dysplasia | rare lung disease, present at birth and treatable by lung transplants |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hemangiosarcoma | rare malignant neoplasm characterized by rapidly proliferating, extensively infiltrating, anaplastic cells derived from blood vessels |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mastocytosis | rare mast cell activation disorder of both children and adults caused by the presence of too many mast cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Trimethylaminuria | rare metabolic disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Degos disease | rare multisystem disease characterized by blockages of small to medium sized blood vessels |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tuberous sclerosis | rare multisystem genetic disease that causes benign tumors to grow in the brain and on other vital organs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Encephalocraniocutaneous lipomatosis | rare neoplastic syndrome characterized by the presence of unilateral lipomas of the cranium, face and neck, and ipsilateral cerebral malformations |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Melkersson–Rosenthal syndrome | rare neurological disorder characterized by recurring facial paralysis, swelling of the face and lips (usually the upper lip - cheilitis granulomatosis) and the development of folds and furrows in the tongue (fissured tongue) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ollier disease | rare nonhereditary sporadic disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | POEMS syndrome | rare paraneoplastic syndrome caused by a clone of aberrant plasma cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gliomatosis cerebri | rare primary brain tumor |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dyskeratosis congenita | rare progressive congenital disorder with a highly variable phenotype |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Urbach–Wiethe disease | rare recessive genetic disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Haphephobia | rare specific phobia that involves the fear of touching or of being touched |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Actinic prurigo | rare sunlight-induced, pruritic, papular or nodular skin eruption |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Junctional ectopic tachycardia | rare syndrome of the heart that manifests in patients recovering from heart surgery: cardiac arrhythmia, or irregular beating of the heart, caused by abnormal conduction from or through the atrioventricular node |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Craniopagus parasiticus | rare type of Craniopagus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Inappropriate sinus tachycardia | rare type of cardiac arrhythmia, within the category of supraventricular tachycardia |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Congenital ichthyosiform erythroderma | rare type of the ichthyosis family of skin diseases |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Choroideremia | rare, X-linked recessive form of hereditary retinal degeneration |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypophosphatasia | rare, and sometimes fatal, metabolic bone disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dubin–Johnson syndrome | rare, autosomal recessive, benign disorder that causes an isolated increase of conjugated bilirubin in the serum |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mammary myofibroblastoma | rare, benign tumor of the breast |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Aortopulmonary window | rare, congenital anomaly in the aorta in which a communication exists between the ascending aorta and the pulmonary artery |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ameloblastic carcinoma | rare, cytologically malignant ameloblastoma that may metastasize |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Erythema ab igne | rash of the skin usually caused by the long-term exposure to heat or infrared radiation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cross-reactivity | reaction between an antibody and an antigen that differs from the immunogen |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Jarisch–Herxheimer reaction | reaction to endotoxin-like products released by the death of harmful microorganisms within the body during antimicrobial treatment |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Alpha-gal allergy | reaction to galactose-alpha-1,3-galactose (alpha-gal) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Disability fraud | receipt of payment(s) intended for the disabled from a government agency or private insurance company by one who should not be receiving them |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Autosomal recessive polycystic kidney disease | recessive form of polycystic kidney disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Rectal prolapse | rectal walls have prolapsed to a degree where they protrude out the anus and are visible outside the body |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Kleine–Levin syndrome | recurrent hypersomnia that is characterized by recurring periods of excessive amounts of sleep and altered behavior |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hyposmia | reduced ability to smell and to detect odors |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ductopenia | reduced numbers of intrahepatic bile duct |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Drug resistance | reduction in effectiveness of a drug such as an antimicrobial, anthelmintic or an antineoplastic in curing a disease or condition |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Astigmatism | refractive error characterized by the optics of the eye to focus a point object into a sharp focused image on the retina, has_symptom blurred vision. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Anorexia mirabilis | religious fasting to the point of starvation, particularly of women and girls of the Middle Ages |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Renal cell carcinoma | renal carcinoma that has material basis in the lining of the proximal convoluted renal tubule of the kidney |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Clear cell renal cell carcinoma | renal cell carcinoma that has material basis in cells that appear very pale or clear when examined under microscope |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Papillary renal cell carcinomas | renal cell carcinoma that is characterized by the development of multiple, bilateral papillary renal tumors |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Malarial nephropathy | renal failure attributed to malarial infection |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Renal tubular acidosis | renal tubular transport disease characterized by excess levels of acid in the blood, due to a failure of the kidneys |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Fanconi syndrome | renal tubular transport disease of the proximal renal tubes characterized by glucosuria, phosphaturia, generalized aminoaciduria and HCO3 wasting |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Obstructive sleep apnea | repeated collapse and obstruction of the upper airway during sleep, which results in reduced airflow (hypopnea) or complete airflow cessation (apnea), oxygen desaturation, and arousals from sleep. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Stereotypy | repetitive mechanical repetition of speech or physical activities |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dead arm syndrome | repetitive motion syndrome in people |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sex cord–gonadal stromal tumour | reproductive organ cancer that is located in the sex cord-derived tissues of the ovary and testis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Male genital disease | reproductive system disease that affects male reproductive organs. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Female genital disease | reproductive system disease that impairs the ability to reproduce and is located in the uterus, vagina, cervix, ovaries or fallopian tubes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Antineoplastic resistance | resistance or diminished response of a neoplasm to an antineoplastic agent |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Croup | respiratory condition that is usually triggered by an acute viral infection of the upper airway |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Laryngeal cancer | respiratory system cancer that is located in the larynx |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ischemia | restriction in blood supply to tissues, causing a shortage of oxygen and glucose |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Loeffler endocarditis | restrictive cardiomyopathy that affects the endocardium and occurs with white blood cell proliferation, specifically of eosinophils |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Distributive shock | resulting from an abnormal distribution of blood flow |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Galactocele | retention cyst containing milk or a milky substance that is usually located in the mammary glands |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Spermatocele | retention cyst of a tubule of the rete testis or the head of the epididymis distended with barely watery fluid that contains spermatozoa. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Central retinal artery occlusion | retinal artery occlusion characterized by blockage of blood flow through the central retinal artery |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Retinitis pigmentosa | retinal degeneration characterized by the gradual deterioration of the photoreceptors or the retinal pigment epithelium of the retina leading to progressive sight loss |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Leber's congenital amaurosis | retinal disease that is characterized by nystagmus, sluggish or no pupillary responses, and severe vision loss or blindness |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Familial exudative vitreoretinopathy | retinal vascular disease characterized by the prevention of blood vessel formation at the edges of the retina and the hemorrhage of the blood vessels in the retina |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cytomegalovirus retinitis | retinitis that has material basis in Cytomegalovirus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Trilateral retinoblastoma | retinoblastoma that refers to bilateral retinoblastoma associated with an intracranial primitive neuroectodermal tumor located in the pineal or suprasellar region |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Laryngopharyngeal reflux | retrograde flow of gastric contents to the upper aero-digestive tract, which causes a variety of symptoms, such as cough, hoarseness, and wheezing |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Valentino's syndrome | retroperitoneal perforation of a duodenal ulcer |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Embryonal rhabdomyosarcoma | rhabdomyosarcoma wherein the mesenchymally-derived malignant cells resemble the primitive developing skeletal muscle of the embryo; it occurs most often in the head and neck area or in the genital or urinary organs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Scleroderma | rheumatic disease and collagen disease that involves the abnormal growth of connective tissue, which supports the skin and internal organs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Juvenile idiopathic arthritis | rheumatoid arthritis that involves an autoimmune disease onset in children under 16 which attacks the healthy cells and tissue of located in joint |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Clanging | rhyming word association phenomenon |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cervical rib | rib |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Autosomal dominant hypophosphatemic rickets | rickets characterized by low levels of serum phosphate and elevated levels of ALP and phosphaturia and that has material basis in autosomal dominant inheritance |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lymphocytic choriomeningitis | rodent-borne viral infectious disease that presents as aseptic meningitis, encephalitis or meningoencephalitis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ovarian torsion | rotation of the ovary |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dandruff | scaly white dead skin flakes from the human scalp |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Paranoid schizophrenia | schizophrenia that involves delusions or auditory hallucinations of persecution or being plotted against without thought disorder, disorganized behavior, or affective flattening |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Systemic scleroderma | scleroderma that is characterized by fibrosis (or hardening) of the skin and major organs, as well as vascular alterations, and autoantibodies |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Primary sclerosing cholangitis | sclerosing cholangitis characterized by fibroobliterative inflammation of the biliary tract, leading to cirrhosis and portal hypertension |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Acne | sebaceous gland's disease characterized by areas of blackheads, whiteheads, pimples, greasy skin, and possibly scarring. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Fordyce spots | sebaceous glands that are present in most individuals |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Congenital chloride diarrhea | secretory diarrhea that has material basis in mutation in the SLC26A3 gene |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bronchocele | segment of bronchus that is filled with mucus and completely enclosed so the mucus cannot drain out |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Febrile seizure | seizure associated with a high body temperature |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Simple partial seizure | seizures which affect initially only one hemisphere of the brain |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dysgammaglobulinemia | selective immunoglobulin deficiency disease that is caused by a reduction in some types of gamma globulins |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Isolated primary immunoglobulin M deficiency | selective immunoglobulin deficiency disease thatis a dysgammaglobulinemia resulting from decreased levels of immunoglobulin M (IgM) production to roduction of other antibodies |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Morgellons | self-diagnosed skin condition |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Oligospermia | semen with abnormally low concentration of sperm |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Itch | sensation that causes the desire or reflex to scratch |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Eye neoplasm | sensory system cancer located in the eye that is characterized by uncontrolled cellular proliferation in the eye |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sinophobia | sentiment against China, its people, overseas Chinese, or Chinese culture |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sequence (medicine) | series of medical consequences due to a single cause |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Acute flaccid myelitis | serious condition of the spinal cord, with symptoms such as rapid onset of arm or leg weakness and decreased reflexes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gluten-related disorders | set of diseases caused by gluten ingestion |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Trinucleotide repeat disorder | set of genetic disorders caused by trinucleotide repeat expansion, a kind of mutation where trinucleotide repeats in certain genes or introns exceed the normal, stable threshold, which differs per gene |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Addictive personality | set of personality traits that make an individual predisposed to developing addictions |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Microhydranencephaly | severe abnormality of brain development characterized by both microcephaly and hydranencephaly |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Anaphylaxis | severe allergic reaction |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Reactive attachment disorder | severe and relatively uncommon disorder that can affect children |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Delirium | severe confusion that develops quickly, and often fluctuates in intensity, neurocognitive disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dipygus | severe congenital deformity |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Starvation | severe deficiency in caloric energy, nutrient, and vitamin intake |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Acne fulminans | severe form of acne |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Global aphasia | severe form of brain damage |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Niemann–Pick disease | severe metabolic disorders in which sphingomyelin accumulates in lysosomes in cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | HELLP syndrome | severe pre-eclampsia characterized by hemolysis, elevated liver enzyme and low platelet count |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Paroxysmal nocturnal dyspnoea | severe shortness of breath and coughing that generally occur at night |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Leydig cell tumour | sex cord-stromal tumour group of ovarian and testicular cancers |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Androgen insensitivity syndrome | sex differentiation condition |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sexual fetishism | sexual arousal a person receives from an object or situation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Emetophilia | sexual arousal from vomiting, or watching others vomit |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Spectrophilia | sexual attraction to ghosts or sexual arousal from images in mirrors |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gerontophilia | sexual attraction toward the elderly. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypoactive sexual desire disorder | sexual dysfunction |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hand fetishism | sexual fascination with hands |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Narratophilia | sexual fetish |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Diaper fetishism | sexual fetish in which a person feels a desire to wear or use diapers |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Salirophilia | sexual fetish or paraphilia that involves deriving erotic pleasure from soiling or disheveling the object of one's desire |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Underwear fetishism | sexual fetishism relating to undergarments |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Breast fetishism | sexual interest focused on female breasts |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Voyeurism | sexual interest in or practice of spying on people engaged in intimate behaviors |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Blood fetishism | sexual interest or paraphilia for blood in clinical vampirism, or within BDSM or vampire lifestyle[ |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Partialism | sexual interest with an exclusive focus on a specific part of the body other than the genitals |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Acrotomophilia | sexual preference |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Genital wart | sexually transmitted disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lymphogranuloma venereum | sexually transmitted disease caused by the invasive serovars L1, L2, L2a or L3 of Chlamydia trachomatis. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chlamydia | sexually transmitted infection caused by the bacterium Chlamydia trachomatis. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Folie à deux | shared psychosis, a psychiatric syndrome in which symptoms of a delusional belief are transmitted from one individual to another |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Saber shin | sharp anterior bowing, or convexity, of the tibia |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Brachycephaly | short head due to premature fusion of the coronal sutures |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Acute bronchitis | short-term inflammation of the bronchi (large and medium-sized airways) of the lungs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Wooden chest syndrome | side effect from opioids |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bovine viral diarrhea | significant economic disease of cattle caused by two species of Pestivirus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tokophobia | significant fear of childbirth |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Inflammation | signs of activation of the immune system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hepatosplenomegaly | simultaneous enlargement of both the liver (hepatomegaly) and the spleen (splenomegaly) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Coinfection | simultaneous infection of a host by more than one pathogen |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Rhabdomyosarcoma | skeletal muscle cancer that arise from skeletal muscle progenitors |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Winged scapula | skeletal muscle condition around the shoulder blade |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Squamous cell skin cancer | skin carcinoma that has material basis in squamous cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pulicosis | skin condition caused by several species of fleas |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | X-linked ichthyosis | skin condition caused by the hereditary deficiency of the steroid sulfatase (STS) enzyme that affects 1 in 2000 to 1 in 6000 males |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Junctional epidermolysis bullosa (medicine) | skin condition characterized by blister formation within the lamina lucida of the basement membrane zone |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Keratosis pilaris | skin condition characterized by small bumps |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Paroxysmal hand hematoma | skin condition characterized by spontaneous focal hemorrhage into the palm or the volar surface of a finger |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Perforating folliculitis | skin condition involving mainly the hairy parts of the extremities |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Trench foot | skin condition of the foot |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Orthostatic purpura | skin condition that results from prolonged standing or even sitting with the legs lowered (as in a bus, airplane, or train), which produced edema and a purpuric eruption on the lower extremities. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Skin infection | skin disease caused by bacteria, fungi, parasites, or viruses |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chloracne | skin disease caused by chlorinated organic compounds |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | White sponge nevus | skin disease characterized by a defect in the normal process of keratinization of the mucosa |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Kindler syndrome | skin disease characterized by congenital blistering, skin atrophy, photosensitivity, skin fragility, and scaling |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Keratosis | skin disease characterized by growth of keratin on the skin or mucous membranes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hives | skin disease characterized by skin rash notable for pale red, raised and itchy bumps, located in the upper dermis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cutis laxa | skin disease characterized by skin that is loose, hanging, wrinkled and lacking in elasticity; it can also affect connective tissue in other parts of the body, including the heart, blood vessels, joints, intestines and lungs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Angioedema | skin disease characterized by the rapid swelling of the dermis, subcutaneous tissue, mucosa and submucosal tissues |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pyotraumatic dermatitis | skin disease for cats and dogs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Trichodysplasia spinulosa | skin disease found in immunocompromised patients, caused by TSPyV |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ichthyosis | skin disease in which dry, scaly skin accumulates |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Erythema multiforme | skin disease that is a type of allergic reaction located in skin, which occurs in response to medications, infections, or illness |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Genodermatosis | skin disease that is caused by a modification of the individual's genome |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ichthyosis vulgaris | skin disorder causing dry, scaly skin. It is the most common form of ichthyosis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Angioma serpiginosum | skin hemangioma characterized by the presence of small red dots that cluster together to form a linear or snake-like array or ring-shaped pattern located in the blood vessels of the skin |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Birthmark | skin irregularity appearing around birth |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ecthyma gangrenosum | skin lesion |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Desmoplastic melanoma | skin malanoma that results in nonpigmented lesions located in sun-exposed areas of the body, most commonly on the head and neck |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Central sleep apnea | sleep apnea that is characterized by a malfunction of the basic neurological controls for breathing rate and the failure to give the signal to inhale, causing the individual to miss one or more cycles of breathing |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sleep apnea | sleep disorder characterized by repeated cessation and commencing of breathing that disrupts sleep |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Rapid eye movement sleep behavior disorder | sleep disorder that involves abnormal behavior including the acting out of violent or dramatic dreams during the sleep phase with rapid eye movement |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Advanced sleep phase disorder | sleep disorder that involves an altered circadian rhythm resulting in falling asleep in early evening and awaking very early in the morning |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Narcolepsy | sleep disorder that involves an excessive urge to sleep at inappropriate times, such as while at work |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Periodic limb movement disorder | sleep disorder that involves involuntary limb movement during sleep |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Eschar | slough or piece of dead tissue that is cast off from the surface of the skin |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tabes dorsalis | slow degeneration (specifically, demyelination) of the neural tracts primarily in the dorsal columns (posterior columns) of the spinal cord (the portion closest to the back of the body) and dorsal roots |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Athetosis | slow, involuntary, convoluted, writhing movements of the fingers, hands, toes, and feet and in some cases, arms, legs, neck and tongue |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Micrometastasis | small collection of cancer cells that has spread to another part of the body |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Telangiectasia | small dilated blood vessels[1] near the surface of the skin or mucous membranes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Duodenal cancer | small intestine cancer that is located in the beginning section of the small intestine |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lung nodule | small lesion in the lung |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Blister | small pocket of fluid within the upper layers of the skin |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Wart | small, rough growth resembling a cauliflower or a solid blister, often found on hands |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Inclusion body disease | snake disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tonsillolith | soft aggregates of bacterial and cellular debris that form in the tonsillar crypts, the crevices of the tonsils |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Alveolar soft part sarcoma | soft tissue cancer that is a slow growing tumor of an unknown origin that effects children and effects young adults |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hemangiopericytoma | soft tissue cancer that is a soft tissue sarcoma and originates in the pericytes in the walls of capillaries |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Skin maceration | softening and breaking down of skin resulting from prolonged exposure to moisture |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Craniotabes | softening or thinning of the skull in infants and children |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Myeloid sarcoma | solid tumor composed of immature white blood cells[2] called myeloblasts. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Nodule (medicine) | solid, non-blisterform elevated areas in or under the skin |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypochondriasis | somatoform disorder that involves an excessive preoccupation or worry about having a serious illness. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pain disorder | somatoform disorder that involves chronic pain in one or more areas, and is thought to be caused by psychological stress. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Da Costa's syndrome | somatoform disorder that involves heart disease symptoms without any identifiable physiological abnormatlities. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Somatization disorder | somatoform disorder that involves persistently complaints of varied physical symptoms that have no identifiable physical origin. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chancre | sore |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Glossitis | soreness of the tongue, or more usually inflammation with depapillation of the dorsal surface of the tongue |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Endaural phenomena | sounds that are heard without external acoustic stimulation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Angularis nigra | space or gap seen at the cervical embrasure, below the contact point of some teeth, when the interdental papilla does not fully enclose the space, leading to an aperture between adjacent teeth |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Turf necrotic ring spot | species of fungus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Plague (disease) | specific contagious and frequently fatal human disease caused by Yersinia pestis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Conduct disorder | specific developmental disorder marked by a pattern of repetitive behavior wherein the rights of others or social norms are violated |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Communication disorder | specific developmental disorder that involves specific developmental disorders of speech and language |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Eating disorder | specific developmental disorder that is characterized by abnormal eating habits that may involve either insufficient or excessive food intake to the detriment of an individual's physical and emotional health |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Smoking and pregnancy | specific developmental disorder that is characterized by physical, behavioral and learning birth defects resulting from maternal ingestion of nicotine during pregnancy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Blood-injection-injury type phobia | specific phobia characterized by the display of excessive, irrational fear in response to the sight of blood, injury, or injection |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Spectrophobia | specific phobia involving a morbid fear of mirrors |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Autophobia | specific phobia of isolation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Zoophobia | specific phobia that involves a fear caused by the presence or thought of a specific animal that poses little or no danger at all |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Nosophobia | specific phobia that involves an irrational fear of contracting a disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Torsades de pointes | specific type of abnormal heart rhythm that can lead to sudden cardiac death. It is a polymorphic ventricular tachycardia that exhibits distinct characteristics on the electrocardiogram |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Nasality (disorder) | speech disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Echolalia | speech disorder that involves the automatic repetition of vocalizations made by another person |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Testicular torsion | spermatic cord (from which the testicle is suspended) twists, cutting off the testicle's blood supply |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Metachromatic leukodystrophy | sphingolipidosis characterized by the accumulation of sulfatides in cells, especially the myelin producing cells of the nervous system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Myelitis | spinal cord disease that is characterized by inflammation of the white matter or gray matter of the spinal cord |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Surfer's myelopathy | spinal cord injury caused by hyperextension of the back |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Scoliosis | spinal medical condition |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Spondyloepimetaphyseal dysplasia, Pakistani type | spondyloepimetaphyseal dysplasia that is characterized by short stature, short and bowed lower limbs, mild brachydactyly, kyphoscoliosis, abnormal gait, enlarged knee joints, precocious osteoarthropathy, and normal intelligence |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Kearns–Sayre syndrome | spontaneous occuring or inherited mitochondrial myopathy with a typical onset before 20 years of age |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Splenosis | spontaneous transplantation of splenic tissue to unusual sites after open splenic trauma |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mitochondrial disease | spontaneously occuring or inherited disorder that involves mitochondrial dysfunction |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | African tick bite fever | spotted fever that has material basis in Rickettsia africae, which is transmitted by ticks |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Metastasis | spread of a disease inside a body |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mass psychogenic illness | spread of illness symptoms through a population where there is no viral or bacterial agent responsible for contagion |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Adenosquamous carcinoma | squamous cell carcinoma that contains squamous cells and gland-like cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Verrucous carcinoma | squamous cell carcinoma that is a diffuse, papillary, non metastasizing, well differentiated, malignant neoplasm of epidermis or oral epithelium |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Spindle cell carcinoma | squamous cell carcinoma that is usually composed of the squamous cell type and results in fusiform development of rapidly proliferating cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mania | state of abnormally elevated or irritable mood, arousal, and/or energy levels |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Infestation | state of being invaded or overrun by pests or parasites |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Nicotine dependence | state of dependence upon nicotine |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Monorchism | state of having only one testicle within the scrotum |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Frailty syndrome | state of increased vulnerability to stressors, following declines in function and reserves across multiple physiologic systems |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Apathy | state of indifference or the suppression of emotions; lack of interest or enthusiasm |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Irritation | state of inflammation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Depression (mood) | state of low mood and fatigue |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Amphetamine dependence | state of psychological dependence on a drug in the amphetamine class |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypovolemic shock | state of shock caused by a decrease in circulating blood volume |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lethargy | state of tiredness, weariness, fatigue, or lack of energy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Coma | state of unconsciousness |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Myocardial stunning | state when some section of the myocardium (corresponding to area of a major coronary occlusion) shows a form of contractile abnormality |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Balding | state where most or all of hair from the head has been lost |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Steatohepatitis | steatotis hepatis macrovezacularis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Blindism | stereotypies characteristic of blind people |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Congenital adrenal hyperplasia | steroid inherited metabolic disorder that is characterized by adrenal insufficiency and variable degrees of hyper or hypo androgeny manifestations resulting from steroidogenic enzyme deficiency |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gastritis | stomach disease that is an inflammation of the lining of the stomach. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Aphthous stomatitis | stomatitis characterized by the repeated formation of benign and non-contagious mouth ulcers |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Kidney stone disease | stone outcome of kidney stone disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Stranger anxiety | stranger ansity |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Silent stroke | stroke that does not have any outward symptoms |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Disabilities affecting intellectual abilities | subnormal intellectual functioning (cognitive disorder) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Contagious disease | subset category of transmissible diseases, which are transmitted to other persons |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Alcohol abuse | substance abuse that involves the recurring use of alcoholic beverages despite negative consequences |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Opioid use disorder | substance abuse that involves the recurring use of opioid drugs despite negative consequences |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Withdrawal syndrome | substance-related disorder that occurs upon the abrupt discontinuation/separation or a decrease in dosage of the intake of medications, recreational drugs, and alcohol |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Anxiety/aggression-driven depression | subtype of Major depressive disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Erotomania | subtype of a delusional disorder, characterized by delusions of another person (possibly imaginary) being infatuated with the patient; commonly, the onset is sudden and the course is chronic |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pathological demand avoidance | subtype of autism |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mixed cerebral palsy | subtype of cerebral palsy characterized by both the tight muscle tone of spastic cerebral palsy and the writhing, involuntary muscle movements of athetoid cerebral palsy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ship foot | subungual hematoma of a toe |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Drop attack | sudden fall without loss of consciousness |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cardiac arrest | sudden stop in effective blood flow due to the failure of the heart to contract effectively |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tinea nigra | superficial fungal infection that causes dark brown to black painless patches on the palms of the hands and the soles of the feet |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Black piedra | superficial mycosis that is a superficial fungal infection of the hair shaft caused by Piedraia hortae |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Spigelian hernia | surgical case |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Clipping (medicine) | surgical procedure performed to treat an aneurysm |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dysphagia | swallowing disorders |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Myoepithelioma of the head and neck | sweat gland neoplasm that is composed of outgrowths of myoepithelial cells from a sweat gland |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hematidrosis | sweating of blood |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Winterbottom's sign | swelling of lymph nodes (lymphadenopathy) along the back of the neck, in the posterior cervical chain of lymph nodes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Goitre | swelling of the thyroid gland |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Porcine enzootic pneumonia | swine disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pseudorabies | swine viral disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Angor animi | symptom defined as a patient's perception that they are dying |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Argyll Robertson pupil | symptom of human disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Intermittent claudication | symptom that describes muscle pain on mild exertion (ache, cramp, numbness or sense of fatigue) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Premenstrual syndrome | symptoms that occur before a woman's period |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Parkinsonism | symptoms that resemble Parkinson's disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Synpolydactyly | syndactyly characterized by an increased number of digits; often a result of a mutation in the HOX D13 gene |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gulf War syndrome | syndrome affecting returning military veterans and civilian workers of the Gulf War |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ochronosis | syndrome caused by the accumulation of homogentisic acid in connective tissues |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Toxidrome | syndrome caused from toxic exposures |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Multiple hamartoma syndrome | syndrome characterized as a spectrum of disorders (Cowden syndrome, Bannayan-Riley-Ruvalcaba syndrome, PTEN-related Proteus syndrome, and Proteus-like syndrome) caused by germline mutations of the PTEN gene |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Usher syndrome | syndrome characterized by a combination of hearing loss and visual impairment |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bruck syndrome | syndrome characterized by a combination of multiple joint contractures and osteogenesis imperfecta |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Reye syndrome | syndrome characterized by acute brain damage and liver function problems |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | CREST syndrome | syndrome characterized by calcinosis, Raynaud's phenomeno, esophageal dysmotility, sclerodactyly and telangiectasia |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Costello syndrome | syndrome characterized by craniofacial dysmorphology, cardiac defects, mild mental retardation, and high birth weight followed by a failure to thrive and developmental delays |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Adams–Oliver syndrome | syndrome characterized by defects of the scalp (aplasia cutis congenita), abnormalities of the fingers, toes, arms and legs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Shwachman–Diamond syndrome | syndrome characterized by exocrine pancreatic insufficiency, bone marrow failure and skeletal abnormalities |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Polycystic ovary syndrome | syndrome characterized by hyperandrogenism, polycystic ovaries, hirsutism, oligomenorrhea or amenorrhea, anovulation and excessive body weight |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Robinow syndrome | syndrome characterized by mild to moderate short stature due to growth delays after birth, distinctive craniofacial abnormalities, skeletal malformations and genital abnormalities |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cronkhite–Canada syndrome | syndrome characterized by multiple polyps of the digestive tract |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Beckwith–Wiedemann syndrome | syndrome characterized by overgrowth (macrosomia), an increased risk of childhood cancer and congenital malformations |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Esophageal rupture | syndrome characterized by spontaneous longitudinal transmural rupture of the esophagus, usually in its distal part |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Van der Woude syndrome | syndrome characterized by the combination of lower lip pits, cleft lip with or without cleft palate and cleft palate alone |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Maffucci syndrome | syndrome characterized by the presence of multiple enchondromas (benign growths of cartilage) associated with multiple cavernous hemangiomas and phleboliths |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Facet syndrome | syndrome in which the facet joints cause painful symptoms |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Organic brain syndrome | syndrome or disorder of mental function whose cause is alleged to be known as organic (physiologic) rather than purely of the mind |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Klüver–Bucy syndrome | syndrome resulting from bilateral lesions of the medial temporal lobe |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Paroxysmal sympathetic hyperactivity | syndrome that causes episodes of increased activity of the sympathetic nervous system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Achard syndrome | syndrome that involves arachnodactyly, receding lower jaw, and joint laxity limited to the hands and feet |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Takayasu's arteritis | syndrome that involves inflammation of the aorta that carries blood from the heart to the rest of the body |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cervicocranial syndrome | syndrome that involves occipital head aches, nystagmus on head movement, tinnitus, spasms, blurred vision, corneal hyperaesthesia, and corneal ulcers |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lown–Ganong–Levine syndrome | syndrome that involves pre-excitation of the ventricles due to an accessory pathway providing an abnormal electrical communication from the atria to the ventricles |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Palindromic rheumatism | syndrome that involves sudden and rapidly developing attacks of arthritis with a remission period that results in no joint damage or symptoms |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Fuchs heterochromic iridocyclitis | syndrome that is a chronic unilateral (or rarely bilateral) iridocyclitis appearing with the triad of heterochromia, predisposition to cataracts and glaucoma, and keratitic percipitates on the posterior corneal surface |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Irritable bowel syndrome | syndrome that is a functional bowel disorder characterized by chronic abdominal pain, discomfort, bloating, and alteration of bowel habits in the absence of any detectable organic cause |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Acrocallosal syndrome | syndrome that is an autosomal recessive disorder, which is characterized by corpus callosum agenesis, polydactyly, multiple dysmorphic features, motor and mental retardation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | CHARGE syndrome | syndrome that is characterized by a pattern of congenital anomalies including choanal atresia and malformations of the heart, inner ear, and retina |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Aicardi syndrome | syndrome that is characterized by absence or underdeveloped tissue connecting the left and right halves of the brain, infantile spasms and chorioretinal lacunae, which are defects in the light-sensitive tissue at the back of the eye |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Marshall–Smith syndrome | syndrome that is characterized by advanced bone age, failure to thrive, respiratory problems, dysmorphic facial features, and variable mental retardation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Peters-plus syndrome | syndrome that is characterized by anterior chamber eye anomalies, short limbs with broad distal extremities, characteristic facial features, cleft lip/palate, and variable developmental delay/intellectual disability |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Aagenaes syndrome | syndrome that is characterized by congenital hypoplasia of lymph vessels, which causes lymphedema of the legs and recurrent cholestasis in infancy, and slow progress to hepatic cirrhosis and giant cell hepatitis with fibrosis of the portal tracts |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Wissler's syndrome | syndrome that is characterized by four typical symptoms: polymorphous exanthemas, recurrent high fever, leucocytosis and arthralgia |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Qazi–Markouizos syndrome | syndrome that is characterized by hypotonia, congenital fiber type disproportion and dysharmonic skeletal maturation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Klippel–Trénaunay syndrome | syndrome that is characterized by large cutaneous hemangiomata with hypertrophy of the related bones and soft tissues |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Berdon syndrome | syndrome that is characterized by marked dilatation of the bladder and microcolon and decreased intestinal peristalsis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Noonan syndrome | syndrome that is characterized by mildly unusual facial features, short stature, heart defects, bleeding problems, skeletal malformations, and many other signs and symptoms |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Multicentric reticulohistiocytosis | syndrome that is characterized by papulonodular skin lesions containing a proliferation of true macrophages associated with arthritis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Zollinger–Ellison syndrome | syndrome that is characterized by the development of a one or more tumors (gastrinoma) in the pancreas, duodenum, or both that secrete excessive levels of gastrin, a hormone that stimulates production of acid by the stomach |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | VACTERL association | syndrome that is characterized by the presence of at least three of the following: vertebral defects, anal atresia, cardiac defects, tracheo-esophageal fistula, renal anomalies, and limb abnormalities |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sudden infant death syndrome | syndrome that is characterized by the sudden death of an infant that is not predicted by medical history and remains unexplained after a thorough forensic autopsy and detailed death scene investigation. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Radiation enteropathy | syndrome that may develop following abdominal or pelvic radiation therapy for cancer. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Psoriatic arthritis | syndrome that occurs in humans with psoriasis who also experience symptoms similar to arthritis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Felty's syndrome | syndrome that results in rheumatoid arthritis, splenomegaly and neutropenia |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tonic tensor tympani syndrome | syndrome where the tensor tympani activates at lower volumes cause frequent spasm |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Shoulder impingement syndrome | syndrome which occurs when the tendons of the rotator cuff muscles become irritated and inflamed as they pass through the subacromial space, the passage beneath the acromion |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Polymyalgia rheumatica | syndrome with pain or stiffness, usually in the neck, shoulders, upper arms, and hips, but which may occur all over the body |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mental retardation and microcephaly with pontine and cerebellar hypoplasia | syndromic X-linked intellectual disability characterized by severe intellectual disability, microcephaly with pontine and cerebellar hypoplasia that has material basis in heterozygous mutation or deletion in the CASK gene on chromosome Xp11 |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | X-linked intellectual disability | syndromic intellectual characterized by an X-linked inheritance pattern |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Baller–Gerold syndrome | synostosis characterized by coronal craniosynostosis, short stature, and aplasia or hypoplasia of the radial bone |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Craniosynostosis | synostosis that results in premature fusion located in skull |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Syndactyly | synostosis that results in the fusion of two or more digits |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Synovial sarcoma | synovium cancer which develops in the synovial membrane of the joints |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Congenital syphilis | syphilis that results in a multisystem infection in the fetus via the placenta |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Collagen disease | systemic autoimmune diseases (e.g., rheumatoid arthritis, systemic lupus erythematosus, and systemic sclerosis), but now is thought to be more appropriate for diseases associated with defects in collagen, which is a component of the connective tissue |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Systemic disease | systemic disease is one that affects a number of organs and tissues, or affects the body as a whole |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Endothelial dysfunction | systemic pathological state of the endothelium |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | SLAP tear | tear of the superior glenoid labrum from anterior to posterior |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dissection (medical) | tear within the wall of a blood vessel |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dentin dysplasia | teeth hard tissue disease characterized by presence of normal enamel but atypical dentin with abnormal pulpal morphology |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Impacted wisdom teeth | teeth that do not fully grow out of the gums due to being blocked by other teeth |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pressure of speech | tendency to speak rapidly and frenziedly, as if motivated by an urgency not apparent to the listener |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Achilles tendinitis | tendonitis of the Achilles tendon |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Neurosis | term and disease in psychology |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Clutton's joints | term describing the finding of symmetrical joint swelling seen in patients with congenital syphilis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Moron (psychology) | term once used in psychiatry to denote mild intellectual disability |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Repeated implantation failure | term that refers to the failure of the embryo to implant onto the side of the uterus wall following IVF treatment |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | TOFI | term used in medicine |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mongrel complex | term used to describe a national inferiority complex in Brazil |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Beta thalassemia | thalassemia characterized by the reduced or absent synthesis of the beta globin chains of hemoglobin |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ventricular remodeling | the changes in size, shape, structure, and function of the heart |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Urethral hypermobility | the condition whereby the female urethra is unstable |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Heterotopia (medicine) | the displacement of an organ from its normal position |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Confabulation | the filling of memory gaps with fabricated, misinterpreted or distorted memories |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Anosmia | the inability to smell |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Carditis | the inflammation of the heart or its surroundings |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Osteochondroma | the most common benign tumors of the bones |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Rolandic epilepsy | the most common epilepsy syndrome in childhood which usually subsides with age |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lentigo simplex | the most common form of lentigo |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Oligodactyly | the presence of four or fewer digits on a hand or foot |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cynanthropy | the supposed magical practice of shape-shifting alternately between canine and human form |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Benzodiazepine use disorder | the use of benzodiazepines without a prescription, often for recreational purposes, which poses risks of dependence, withdrawal and other long-term effects |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Callus | thickened and hardened area of skin |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hyperkeratosis | thickening of the stratum corneum (the outermost layer of the epidermis), often associated with the presence of an abnormal quantity of keratin |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Arteriosclerosis | thickening, hardening and loss of elasticity of the walls of arteries |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Breast disease | thoracic disease that is located in the breast |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Derailment (thought disorder) | thought disorder in psychiatry |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tangentiality | thought disorder, involves replying to a question in an oblique, irrelevant or tangential manner |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Thought blocking | thought disorder, sudden gaps or stoppages in train of thought |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Paranoia | thought process believed to be heavily influenced by anxiety or fear, often to the point of delusion and irrationality |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Congenital amegakaryocytic thrombocytopenia | thrombocytopenia characterized by a severe reduction in megakaryocyte and platelet numbers that has material basis in homozygous or compound heterozygous mutation in the MPL gene on chromosome 1p34 |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Follicular thyroid cancer | thyroid carcinoma that has material basis in follicular cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Papillary thyroid cancer | thyroid carcinoma that is characterized by the small mushroom shape of the tumor which has a stem attached to the epithelial layer |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hyperthyroidism | thyroid gland disease that involves an over Production of thyroid hormone. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ehrlichiosis (canine) | tick-borne disease of dogs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tick paralysis | tick-borne disease that is not caused by an infectious organism |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Endothrix | tinea capitis that results in fungal infection located in hair, has material basis in Ascomycota fungi that belong to a group called dermatophytes, which produce arthroconidia within the hair shaft only |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tinea imbricata | tinea corporis that results in fungal infection located in skin, has material basis in Trichophyton concentricum, which is characterized by ring-like growth in overlapping circles that may have an autosomal dominant genetic predisposition |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Drusen | tiny yellow or white accumulations of extracellular material that build up between Bruch's membrane and the retinal pigment epithelium of the eye |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Reperfusion injury | tissue damage caused when blood supply returns to the tissue after a period of ischemia or lack of oxygen (anoxia, hypoxia) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dermoid cyst | tissue disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Caviar tongue | tongue disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tonsil carcinoma | tonsil cancer that has material basis in squamous cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dental abscess | tooth disease characterized by a localized collection of pus associated with a tooth |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypodontia | tooth disease characterized by failure to develop on or more missing teeth |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Barodontalgia | tooth pain caused by pressure |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ageusia | total loss of the sense of taste |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Stupor | total or nearly total lack of spontaneous movements (disease) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Joint stiffness | toughness |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Thallium poisoning | toxic effects of thallium |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tracheomalacia | tracheal disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Drug diversion | transfer of legally prescribed controlled pharmaceuticals to other individuals |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Thousand-yard stare | trauma symptom |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hand injury | trauma to the han |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Vertebral artery dissection | traumatic or nontraumatic vertebral artery rupture |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tricuspid atresia | tricuspid valve disease characterized by a missing or abnormally developed tricuspid heart value at birth |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ebstein's anomaly | tricuspid valve disease that is a congenital heart defect in which the septal leaflet of the tricuspid valve is displaced towards the apex of the right ventricle of the heart |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Buruli ulcer | tropical disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dengue fever | tropical disease caused by the dengue virus, transmitted by mosquito |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lymphatic filariasis | tropical helminthiasis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Multi-drug-resistant tuberculosis | tuberculosis that is resistant to isoniazid and rifampicin, the two most powerful first-line anti-TB drugs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mediastinal tumor | tumor in the mediastinum area of the body |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hemangioblastoma | tumor of the central nervous system that originates from the vascular system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pancoast tumor | tumor of the pulmonary apex. It is a type of lung cancer defined primarily by its location situated at the top end of either the right or left lung. It typically spreads to nearby tissues such as the ribs and vertebrae |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bone tumor | tumor or cancer located in bone tissue or specific bones |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Kidney tumour | tumor or cancer of the kidney |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tumors of the hematopoietic and lymphoid tissues | tumor that affect the blood, bone marrow, lymph, and lymphatic system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ependymoma | tumor that arises from the ependyma, a tissue of the central nervous system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pelvic tumor | tumors or cancer of the pelvic region |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Renal oncocytoma | tumour of the kidney made up of oncocytes, a special kind of cell |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lewy body dementia | two dementias characterized by abnormal deposits of the protein alpha-synuclein in the brain |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Lipoatrophic diabetes | type 2 diabetes that involves severe lipodystrophy in addition to the traditional signs of diabetes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | HL23V | type C RNA tumor virus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Insect sting allergy | type of allergy cause by an insect bite or sting |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Allergy to cats | type of allergy caused by cats |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Drug allergy | type of allergy caused by consumption of a drug |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Garlic allergy | type of allergy caused by garlic |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Oat sensitivity | type of allergy caused by oats |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Familial renal amyloidosis | type of amyloidosis that mostly affects the kidney |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pentasomy X | type of aneuploidy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Unstable angina | type of angina pectoris that is irregular. It is also classified as a type of acute coronary syndrome |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Jargon aphasia | type of aphasia involving noun selection difficulty |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Anomic aphasia | type of aphasia that causes problems with recalling words or names |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Polyarthritis | type of arthritis which involves 5 or more joints simultaneously |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Limp | type of asymmetric abnormality of the gait |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dysmetria | type of ataxia characterized by the inability to carry out movements with the correct range and motion across the plane of more than one joint related to incorrect estimation of the distances required for targeted movements |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cerebral atherosclerosis | type of atherosclerosis where build-up of plaque in the blood vessels of the brain occurs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Degloving | type of avulsion in which an extensive section of skin is completely torn off the underlying tissue |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Warthin's tumor | type of benign tumor of the salivary glands |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cavernous hemangioma | type of blood vessel malformation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Craniopharyngioma | type of brain tumor derived from pituitary gland embryonic tissue that occurs most commonly in children, but also affects adults |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Adenoid cystic carcinoma | type of cancer |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Digestive system neoplasm | type of cancer that afflicts the digestive system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Paget's disease of the breast | type of cancer that outwardly may have the appearance of eczema, with skin changes involving the nipple of the breast. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Small-cell carcinoma | type of carcinoma that commonly arises within lung and sometime other body sites |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ischemic cardiomyopathy | type of cardiomyopathy caused by a narrowing of the coronary arteries which supply blood to the heart |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | White blood cell | type of cells of the immunological system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Spastic cerebral palsy | type of cerebral palsy characterized by increased muscle tone |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Spastic diplegia | type of cerebral palsy characterized by spasticity and hypertonia of the lower extremities bilaterally, particularly the legs, hips, and pelvis; this is the most common (70%) form of cerebral palsy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ecchondroma | type of chondroma that is subperiosteal |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cardiogenic shock | type of circulatory shock resulting from inadequate blood flow due to the dysfunction of the ventricles of the heart |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Minor physical anomalies | type of congenital abnormality |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Congenital abnormality | type of congenital disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Meesmann corneal dystrophy | type of corneal dystrophy and a keratin disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ulcer (dermatology) | type of cutaneous condition |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sézary disease | type of cutaneous lymphoma |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Choroidal fissure cyst | type of cyst |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Psychological trauma | type of damage to the psyche that occurs as a result of a severely distressing event |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | The Truman Show delusion | type of delusion in which the person believes that their lives are staged reality shows, or that they are being watched on cameras |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dementia with Lewy bodies | type of dementia |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Type 2 diabetes | type of diabetes mellitus with high blood sugar and insulin resistance |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Endocrine disease | type of disease affecting the endocrine system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bluetongue disease | type of disease that afflicts ruminants |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Vertigo | type of dizziness |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Fat embolism syndrome | type of embolism |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Thyroid disease | type of endocrine disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Peanut allergy | type of food allergy |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Fruit allergy | type of food allergy caused by fruit |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Milk allergy | type of food allergy caused by milk |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tinea cruris | type of fungal infection of the groin region in either sex, though more often seen in males |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Generalized tonic–clonic seizure | type of generalized seizure |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Oligodendroglioma | type of glioma that are believed to originate from the oligodendrocytes of the brain or from a glial precursor cell |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Esca (grape disease) | type of grapevine trunk disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Alcoholic hallucinosis | type of hallucinosis (pseudo-hallucination) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Junctional tachycardia | type of heart arrhythmia |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Atrial tachycardia | type of heart rhythm problem in which the heart's electrical impulse comes from an ectopic pacemaker |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sickle cell disease | type of hereditary blood disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hiatal hernia | type of hernia in which abdominal organs (typically the stomach) slip through the diaphragm into the middle compartment of the chest |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Adult-onset immunodeficiency syndrome | type of immunodeficiency |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Crohn's disease | type of inflammatory bowel disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Intracerebral hemorrhage | type of intracranial hemorrhage that occurs within the brain tissue itself |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cerebral infarction | type of ischemic stroke resulting from a blockage in the blood vessels supplying blood to the brain |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Uremia | type of kidney disease, urea in the blood |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bronchitis | type of lower respiratory disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Rhinorrhea | type of medical symptom where the nasal cavity is filled with fluid mucus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Suspension trauma | type of medical trauma |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Oligomenorrhea | type of menstrual disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Monocytic leukemia | type of myeloid leukemia characterized by a dominance of monocytes in the marrow |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Fournier gangrene | type of necrotizing fasciitis or gangrene affecting the external genitalia and/or perineum |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Interstitial nephritis | type of nephritis affecting the interstitium of the kidneys surrounding the tubules |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pheochromocytoma | type of neuroendocrine tumor |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Carcinoid | type of neuroendocrine tumor originating in the cells of the neuroendocrine system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Demyelinating disease | type of neurological disease where the myelin sheath of neurons is damaged |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Green Tobacco Sickness | type of nicotine poisoning |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Sebaceous hyperplasia | type of non-malignant skin lesion |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Chronic obstructive pulmonary disease | type of obstructive lung disease characterized by long-term poor airflow |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Middle back pain | type of pain felt between the bottom of the neck and top of the lumbar spine |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Back pain | type of pain felt in the back |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Paruresis | type of phobia in which the sufferer is unable to urinate |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Photophthalmia | type of photokeratitis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hemothorax | type of pleural effusion in which blood accumulates in the pleural cavity |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Atypical pneumonia | type of pneumonia not caused by one of the pathogens most commonly associated with the disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Erythropoietic porphyria | type of porphyria associated with erythropoietic cells. In erythropoietic porphyrias, the enzyme deficiency occurs in the red blood cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Maculopapular rash | type of rash |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Surface dyslexia | type of reading disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Simple-type schizophrenia | type of schizophrenia |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Anorgasmia | type of sexual dysfunction in which a person cannot achieve orgasm despite adequate stimulation |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Saree cancer | type of skin cancer that occurs along the waistline in people wearing the saree |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pityriasis rosea | type of skin rash |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Gelotophobia | type of social phobia consisting in the fear of being laughed at |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Spastic quadriplegia | type of spastic cerebral palsy characterized by increased muscle tone of all four extremities |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Spastic hemiplegia | type of spastic cerebral palsy characterized by increased muscle tone of the arm and leg on the same side of the body |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Brainerd diarrhea | type of sudden-onset watery, explosive diarrhea |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | AV nodal reentrant tachycardia | type of supraventricular tachycardia (SVT), meaning that it originates from a location within the heart above the bundle of His. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Delta-beta thalassemia | type of thalassemia |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Epidural hematoma | type of traumatic brain injury in which a buildup of blood occurs between the dura mater and the skull |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Angiomatoid fibrous histiocytoma | type of tumor which affects children and adolescents |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Non-small-cell lung carcinoma | type of tumour |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pharyngitis | type of upper respiratory tract infection |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Leukorrhea | type of vaginal discharge |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Riddoch syndrome | type of visual impairment |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Murine typhus | typhus transmitted by fleas (Xenopsylla cheopis), usually on rats |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tyrosinemia type III | tyrosinemia that has material basis in deficiency of 4-hydroxyphenylpyruvate dioxygenase disrupting the break down of tyrosine |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tyrosinemia type II | tyrosinemia that has material basis in deficiency of hepatic tyrosine aminotransferase located in the liver and is characterized by keratitis, painful palmoplantar hyperkeratosis, mental retardation, and elevated serum tyrosine levels |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Type I tyrosinemia | tyrosinemia that has material basis in deficiency of the enzyme fumarylacetoacetate hydrolase resulting in an increase in fumarylacetoacetate which inhibits previous steps in tyrosine degradation leading to an accumulation of tyrosine in the body |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Mouth ulcer | ulcer that occurs on the mucous membrane of the oral cavity |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Secondary sclerosing cholangitis | umbrella term for other unrelated medical conditions that cause sclerosis of the bile ducts |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bálint's syndrome | uncommon and incompletely understood triad of severe neuropsychological impairments |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Parkes Weber syndrome | uncommon congenital vascular malformation (CVM) characterized by the venous malformations, cutaneous capillary malformations, and lymphatic malformations along with arteriovenous malformation. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hemophagocytic lymphohistiocytosis | uncommon hematologic disorder seen more often in children than in adults |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hepatoblastoma | uncommon malignant liver cancer occurring in infants and children |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Acute biphenotypic leukaemia | uncommon type of leukemia which arises in multipotent progenitor cells which have the ability differentiating into both myeloid and lymphoid lineages |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Urinary incontinence | uncontrolled leakage of urine |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pancreatic tumor | undifferentiated growth detected in the pancreas |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Spinal cord compression | undue compressive force on the spinal cord |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypereosinophilic syndrome | unexplained chronic eosinophila |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cyberchondria | unfounded escalation of concerns about common symptomology based on review of search results and literature online |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Adverse drug reaction | unintended effect of drugs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Combined drug intoxication | unnatural cause of human death |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hangover | unpleasant physiological and psychological effects following the consumption of ethanol |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Grandiosity | unrealistic sense of superiority and of uniqueness |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Thallium poisoning case of Zhu Ling | unsolved 1995 thallium poisoning case in China |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Micropenis | unusually small penis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Macrostomia | unusually wide mouth |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Xanthochromism | unusually yellow pigmentation in an animal |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Intrusive thought | unwelcome involuntary thought, image, or unpleasant idea that may become an obsession |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Kennel cough | upper respiratory infection affecting dogs |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Feline viral rhinotracheitis | upper respiratory or pulmonary infection of cats |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Adenoid hypertrophy | upper respiratory tract disease characterized by the unusual growth of the adenoid tonsil; has symptom snoring, has symptom hyponasality, has symptom otitis media with effusion, has symptom mouth breathing |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ornithine transcarbamylase deficiency | urea cycle disorder that involves a mutated and ineffective form of the enzyme ornithine transcarbamylase |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Argininemia | urea cycle disorder that involves arginase deficiency resulting in elevated levels of plasma arginine |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Citrullinemia | urea cycle disorder that involves the accumulation of ammonia in the blood. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Vesicoureteral reflux | ureteral disease characterized by backward flow of urine from the urinary bladder into the ureter |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Problem gambling | urge to continuously gamble despite harmful negative consequences or a desire to stop |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Kidney cancer | urinary system cancer that is located in the kidney |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ureteral cancer | urinary system cancer that is located in the ureter |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bladder cancer | urinary system cancer that results in malignant growth located in the urinary bladder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Urinary bladder disease | urinary system disease that is located in the bladder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Kidney disease | urinary system disease that is located in the kidney |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Urethral cancer | urinary tract cancer that derives from the tissues of the urethra |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Nephrogenic adenoma | urologic disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Albuminuria | urologic disease typically indicating kidney malfunction |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Physical urticaria | urticaria induced by external physical influences |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dermatographic urticaria | urticaria induced by stroking of the skin |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cholinergic urticaria | urticaria induced by sweating |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Doping in sport | use of banned performance-enhancing drugs in sports |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Brenner tumour | usually benign tumor composed of solid and cystic nests of epithelial cells resembling transitional epithelium; it is surrounded by an abundant stromal component that is dense and fibroblastic in nature |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Uterine fibroid | uterine benign neoplasm derived from the smooth muscle layer of the uterus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Endometrial hyperplasia | uterine benign neoplasm that is characterized by excessive proliferation of the cells of the endometrium |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Endometrial cancer | uterine cancer that is located in tissues lining the uterus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Uterine sarcoma | uterine corpus cancer that is located in the muscles of the uterus or located in other tissues that support the uterus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Placental disease | uterine disease that is located in the placenta |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pyometra | uterine infection |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Uveal melanoma | uveal cancer that has material basis in uvea pigment cells |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Panphobia | vague and persistent dread of some unknown evil |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tricuspid valve stenosis | valvular heart disease which results in the narrowing of the orifice of the tricuspid valve of the heart |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Factor V Leiden | variant causing increased blood clotting |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Proctalgia fugax | variant of levator ani syndrome |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | SAPHO syndrome | variety of inflammatory bone disorders that may be associated with skin changes |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Central nervous system cavernous hemangioma | vascular anomaly, a collection of large, thin walled tortuous veins, in any part of the central nervous system but lacking intervening nervous tissue |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Air embolism | vascular blockage by air bubbles |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Acrocyanosis | vascular disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Thrombosis | vascular disease caused by the formation of a blood clot inside a blood vessel, obstructing the flow of blood through the circulatory system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Vein disorders | vascular disease located in a vein |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Angiodysplasia | vascular disease that is characterized as a small vascular malformation of the gut |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Cholesterol embolism | vascular disease that is characterized by blood vessel obstruction resulting from the release of cholesterol from the inside of blood vessels along the bloodstream |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Thoracic outlet syndrome | vascular disease that is characterized by compression at the superior thoracic outlet resulting from excess pressure placed on a neurovascular bundle passing between the anterior scalene and middle scalene muscles |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Generalized arterial calcification of infancy | vascular disease that is characterized by generalized calcification of the arterial internal elastic lamina, leading to rupture of the lamina and occlusive changes in the tunica intima with stenosis and decreased elasticity of the vessel wall |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Vasculitis | vascular disease that is characterized by inflammation of the blood vessels |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hemorrhoid | vascular structures in the anal canal |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Erythema elevatum diutinum | vasculitis characterised by red, purple, brown or yellow papules (raised spot), plaques, or nodules, found on the backs of the hands, other extensor surfaces overlying joints, and on the buttocks |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Livedoid vasculitis | vasculitis with purpuric ulcers |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Eosinophilic granulomatosis with polyangiitis | vasculitits that is systemic vasculitis realized as blood vessel inflammation and has_symptom asthma along with hay fever, rash and gastrointestinal bleeding. |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Phlebitis | vein disease that is characterized by inflammation of a vein |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Varicose veins | vein disease that is characterized by swollen, twisted veins visible just under the surface of the skin |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Post-thrombotic syndrome | venous insufficiency that is characterized by aching pain, heaviness, swelling, cramps, itching, or tingling in the affected limb and is a chronic complication of deep venous thrombosis |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ring chromosome 14 syndrome | very rare human chromosome abnormality |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Progressive multifocal leukoencephalopathy | viral disease affecting human brains |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Measles | viral disease affecting humans |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Herpes simplex | viral disease caused by the herpes simplex virus |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Molluscum contagiosum | viral infection of the skin |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Ebola virus disease | viral infectious disease found in humans and other mammals |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Tick-borne encephalitis | viral infectious disease involving the central nervous system |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Plantar wart | viral infectious disease that results in benign epithelial tumors located in skin of the sole or toes of the foot, has material basis in human papillomavirus (types 1, 2, 4 or 63), has symptom lesions that appear on the sole of the foot |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Heck's disease | viral infectious disease that results in infection located in mouth, has material basis in human papillomavirus (types 13 or 32) |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Severe acute respiratory syndrome | viral respiratory disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Middle East respiratory syndrome | viral respiratory infection |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Myrmecia (skin) | virus-related cutaneous foot disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Nevus | visible, circumscribed, chronic lesion of the skin or mucosa, either congenital or acquired |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Dysmetropsia | vision disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Scintillating scotoma | visual aura |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Visual release hallucinations | visual disturbances and the experience of complex visual hallucinations in a blind person |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Visual snow | visual impairment |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Vitamin K deficiency | vitamin k deficiency |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Vitamin B12 deficiency | vitamin metabolic disorder that results from low blood levels of vitamin B12 |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hoarse voice | voice disorder |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Bartholin gland carcinoma | vulva carcinoma that has material basis in abnormally proliferating cells derives from epithelial cells and is located in Bartholin's gland |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Vulvitis | vulva disease |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hemiparesis | weakness of one side of the body |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Hypoglycemia | when blood sugar decreases to below normal levels |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Acute generalized exanthematous pustulosis | widespread acute rash characterized by fever and multiple small pustules on a reddish background |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Pterygium (conjunctiva) | winglike triangular membrane occurring in the neck, eyes, knees, elbows, ankles or digits |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Eco-anxiety | worry over climate change |
1 | Wikipedia:WikiProject Short descriptions/wd/get list | Insect bites and stings | wound caused by the bite of an insect |