Wikipedia:WikiProject Missing encyclopedic articles/Missing diseases/4
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- D'ercole syndrome
- Daish Hardman Lamont syndrome
- Dandy-walker malformation with mental retardation, basal ganglia disease, and seizures
- Dandy-walker malformation with mental retardation, macrocephaly, myopia, and brachytelephalangy
- Daneman Davy Mancer syndrome
- Davenport Donlan syndrome
- Davis Lafer syndrome
- Deafness conductive stapedial ear malformation facial palsy
- Deafness epiphyseal dysplasia short stature
- Deafness goiter stippled epiphyses
- Deafness hyperuricemia neurologic ataxia
- Deafness hypogonadism syndrome
- Deafness hypospadias metacarpal and metatarsal syndrome
- Deafness mesenteric diverticula of small bowel neuropathy
- Deafness nephritis ano rectal malformation
- Deafness neurosensory pituitary dwarfism
- Deafness oligodontia syndrome
- Deafness onychodystrophy dominant form
- Deafness peripheral neuropathy arterial disease
- Deafness symphalangism
- Deafness white hair contractures papillomas
- Deal Barratt Dillon syndrome
- Defective expression of HLA class 2
- Degenerative optic myopathy
- Delayed membranous cranial ossification
- Delayed speech facial asymmetry strabismus ear lobe creases
- Deletion 6q16 q21
- Delta-1-pyrroline-5-carboxylate dehydrogenase deficiency
- Dementia progressive lipomembranous polycysta
- Dennis Cohen syndrome
- Dennis Fairhurst Moore syndrome
- Dentin dysplasia sclerotic bones
- Der Kaloustian Mcintosh Silver syndrome
- Dermatocardioskeletal syndrome Boronne type
- Dermatoleukodystrophy
- Dermochondrocorneal dystrophy of François
- Desbuquois syndrome - double check redirect of Desbuquois Syndrome
- Developmental delay hypotonia extremities hypertrophy
- Developmental dysphasia familial
- Devriendt Legius Fryns syndrome
- Devriendt Vandenberghe Fryns syndrome
- Diabetes persistent mullerian ducts
- Diaphragmatic agenesia
- Diaphragmatic agenesis radial aplasia omphalocele
- Diaphragmatic defect limb deficiency skull defect
- Diaphragmatic hernia upper limb defects
- Diarrhea chronic with villous atrophy
- Die Smulders Droog Van Dijk syndrome
- Die Smulders Vles Fryns syndrome
- Digestive duplication
- Dincsoy Salih Patel syndrome
- Dinno Shearer Weisskopf syndrome
- Diphallus rachischisis imperforate anus
- Diphosphoglycerate mutase deficiency of erythrocyte
- Disorder in the hormonal synthesis with or without goiter
- Disorganization syndrome
- Dobrow syndrome
- Dominant zonular cataract
- Double fingernail of fifth finger
- Double outlet left ventricle
- Drachtman Weinblatt Sitarz syndrome
- Duker Weiss Siber syndrome
- Duodenal atresia tetralogy of Fallot
- Duplication of leg mirror foot
- Duplication of the thumb unilateral biphalangeal
- Duplication of urethra
- Dupont Sellier Chochillon syndrome
- Dwarfism deafness retinitis pigmentosa
- Dwarfism lethal type advanced bone age
- Dwarfism mental retardation eye abnormality
- Dwarfism short limb absent fibulas very short digits
- Dwarfism stiff joint ocular abnormalities
- Dwarfism syndesmodysplasic
- Dwarfism tall vertebrae
- Dwarfism thanatophoric
- Dwarfism thin bones multiple fractures
- Dyggve-Melchior-Clausen syndrome
- Dykes Markes Harper syndrome
- Dyschondrosteosis nephritis
- Dysmorphism abnormal vocalization mental retardation
- Dysmorphism cleft palate loose skin
- Dysphasic dementia, hereditary
- Dysplastic cortical hyperostosis
- Dysraphism cleft lip palate limb reduction defects
- Dyssegmental dysplasia glaucoma
- Dyssegmental dysplasia Silverman Handmaker type
- Ectodermal dysplasia adrenal cyst
- Ectodermal dysplasia alopecia preaxial polydactyly
- Ectodermal dysplasia arthrogryposis diabetes mellitus
- Ectodermal dysplasia Bartalos type
- Ectodermal dysplasia Berlin type
- Ectodermal dysplasia blindness
- Ectodermal dysplasia Margarita type
- Ectodermal dysplasia mental retardation CNS malformation
- Ectodermal dysplasia mental retardation syndactyly
- Ectodermal dysplasia neurosensory deafness
- Ectodermal dysplasia osteosclerosis
- Ectodermal dysplasia tricho odonto onychial type
- Ectopia pupillae
- Ectopic coarctation
- Ectrodactyly cardiopathy dysmorphism
- Ectrodactyly diaphragmatic hernia corpus callosum
- Ectropion inferior cleft lip and or palate
- Edinburgh malformation syndrome
- Edwards Patton Dilly syndrome
- Egg shaped pupils
- Elliott Ludman Teebi syndrome
- Ellis Yale Winter syndrome
- Emphysema-penoscrotal web-deafness-mental retardation
- Enamel hypoplasia cataract hydrocephaly
- Encephalopathy intracerebral calcification retinal
- Encephalophathy recurrent of childhood
- Enchondromatosis dwarfism deafness
- Eng Strom syndrome
- Engelhard Yatziv syndrome
- Englemann disease - possibly Camurati–Engelmann disease?
- Enterovirus antenatal infection
- Eosinophilic cryptitis
- Eosinophilic synovitis
- Epidermal nevus vitamin D resistant rickets
- Epidermolysis bullosa simplex with anodontia, hair
- Epidermolytic palmoplantar keratoderma Vorner type
- Epilepsy microcephaly skeletal dysplasia
- Epilepsy occipital calcifications
- Epilepsy telangiectasia
- Epimetaphyseal dysplasia cataract
- Epiphyseal dysplasia dysmorphism camptodactyly
- Epiphyseal dysplasia hearing loss dysmorphism
- Eronen Somer Gustafsson syndrome
- Erythroderma lethal congenital
- Esophageal atresia coloboma talipes
- Euhidrotic ectodermal dysplasia
- Exostoses anetodermia brachydactyly type E
- Extrasystoles short stature hyperpigmentation microcephaly
- Eye defects arachnodactyly cardiopathy
- Eyebrows duplication syndactyly