Category:C-Class medical genetics articles
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Pages in category "C-Class medical genetics articles"
The following 200 pages are in this category, out of approximately 287 total. This list may not reflect recent changes.
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- Talk:1q21.1 deletion syndrome
- Talk:1q21.1 duplication syndrome
- Talk:2-Hydroxyglutaric aciduria
- Talk:2-Methylbutyryl-CoA dehydrogenase deficiency
- Talk:2p15-16.1 microdeletion syndrome
- Talk:2q37 deletion syndrome
- Talk:3-M syndrome
- Talk:3-Methylglutaconic aciduria
- Talk:6-phosphogluconate dehydrogenase deficiency
- Talk:6-Pyruvoyltetrahydropterin synthase deficiency
- Talk:9q34.3 deletion syndrome
- Talk:13q deletion syndrome
- Talk:22q11.2 distal deletion syndrome
- Talk:22q11.2 duplication syndrome
- Talk:22q13 deletion syndrome
- Talk:23andMe
- Talk:45,X/46,XY mosaicism
- Talk:46,XX/46,XY
- Talk:100,000 Genomes Project
A
- Talk:Aagenaes syndrome
- Talk:ABCD syndrome
- Talk:Abetalipoproteinemia
- Talk:Ablepharon macrostomia syndrome
- Talk:Achondrogenesis type 1B
- Talk:Achondroplasia in children
- Talk:Acrokeratosis verruciformis
- Talk:Adenylosuccinate lyase deficiency
- Talk:African Centre of Excellence for Genomics of Infectious Diseases
- Talk:African iron overload
- Talk:Aicardi–Goutières syndrome
- Talk:Alagille syndrome
- Talk:Albinism in humans
- Talk:Aldolase A deficiency
- Talk:Alkaptonuria
- Talk:Alpha-1 antitrypsin deficiency
- Talk:Alström syndrome
- Talk:Alternating hemiplegia of childhood
- Talk:Amelogenesis imperfecta
- Talk:Apert syndrome
- Talk:Apparent mineralocorticoid excess syndrome
- Talk:Aromatase deficiency
- Talk:Hans Asperger
- Talk:Autism-Europe
- Talk:Autophagic vacuolar myopathy
- Talk:Autosomal dominant cerebellar ataxia
- Talk:Autosomal dominant nocturnal frontal lobe epilepsy
- Talk:Autosomal dominant porencephaly type I
B
- Talk:Bannayan–Riley–Ruvalcaba syndrome
- Talk:Bardet–Biedl syndrome
- Talk:Bare lymphocyte syndrome type II
- Talk:Bartter syndrome
- Talk:Beckwith–Wiedemann syndrome
- Talk:Benign familial neonatal seizures
- Talk:Benign hereditary chorea
- Talk:Bifid nose
- Talk:Bochdalek hernia
- Talk:Brown–Vialetto–Van Laere syndrome
- Talk:Ed Byrne (neuroscientist)
C
- Talk:CADASIL
- Talk:Camurati–Engelmann disease
- Talk:Canavan disease
- Talk:Carnitine palmitoyltransferase II deficiency
- Talk:Carpenter syndrome
- Talk:Carrier testing
- Talk:Causes of autism
- Talk:CCR5
- Talk:Charcot–Marie–Tooth disease
- Talk:CHCHD10
- Talk:Chromosome 1
- Talk:Chromosome 2
- Talk:Chromosome 21
- Talk:Chromosome instability
- Talk:Chronic granulomatous disease
- Talk:Ciliopathy
- Talk:Clinodactyly
- Talk:Cockayne syndrome
- Talk:Codon degeneracy
- Talk:Colorectal polyp
- Talk:Compound heterozygosity
- Talk:Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency
- Talk:Congenital distal spinal muscular atrophy
- Talk:Conorenal syndrome
- Talk:Control of chromosome duplication
- Talk:Cornea plana 1
- Talk:Cornea plana 2
- Talk:Coronary artery anomaly
- Talk:Costello syndrome
- Talk:Cranio-lenticulo-sutural dysplasia
- Talk:Craniofacial cleft
- Talk:Crigler–Najjar syndrome
- Talk:Crisscross heart
- Talk:Crouzon syndrome
D
E
F
- Talk:Fabry disease
- Talk:Factor V Leiden
- Talk:Familial dysautonomia
- Talk:Familial Mediterranean fever
- Talk:Familial opposable triphalangeal thumbs duplication
- Talk:Fanconi anemia
- Talk:Alessio Fasano
- Talk:Floating–Harbor syndrome
- Talk:Focal facial dermal dysplasia
- Talk:FOSB
- Talk:Fraser syndrome
- Talk:Frontotemporal dementia and parkinsonism linked to chromosome 17
- Talk:Fryns syndrome
- Talk:Fukuyama congenital muscular dystrophy
G
- Talk:Galactosemia
- Talk:Galactosialidosis
- Talk:Ayelet Galena
- Talk:Gene duplication
- Talk:Gene therapy for color blindness
- Talk:Gene therapy for epilepsy
- Talk:Gene therapy in Parkinson's disease
- Talk:Genetic counseling
- Talk:Genetic epidemiology
- Talk:Genetic marker
- Talk:Genetics of social behavior
- Talk:Genodermatosis
- Talk:Germline mosaicism
- Talk:Gilbert's syndrome
- Talk:Glycogen storage disease type I
- Talk:Glycogen storage disease type II
- Talk:Glycogen storage disease type III
- Talk:Glycogen storage disease type IX
- Talk:Gonadotropin-releasing hormone insensitivity
H
- Talk:Haemophilia
- Talk:Haemophilia B
- Talk:Haemophilia C
- Talk:Haemophilia in European royalty
- Talk:Hajdu–Cheney syndrome
- Talk:Halperin-Birk syndrome
- Talk:Harlequin-type ichthyosis
- Talk:Hemoglobin Hopkins-2
- Talk:Hereditary fructose intolerance
- Talk:Hereditary inclusion body myopathy
- Talk:Hereditary motor and sensory neuropathy
- Talk:Hereditary multiple exostoses
- Talk:Hereditary nonpolyposis colorectal cancer
- Talk:Hereditary pancreatitis
- Talk:Hereditary spastic paraplegia
- Talk:Heritability
- Talk:Heteroplasmy
- Talk:Hirschsprung's disease
- Talk:History of Tay–Sachs disease
- Talk:Andrew Holding
- Talk:Homocystinuria
- Talk:Human behaviour genetics
- Talk:Human disease modifier gene
- Talk:Hunter syndrome
- Talk:Hurler syndrome
- Talk:Hypochondroplasia
- Talk:Hypokalemic periodic paralysis