Category:Autosomal dominant disorders
For more information on autosomal dominant heredity, see the articles Autosome and Dominance (genetics).
Wikimedia Commons has media related to Autosomal dominant diseases and disorders.
Subcategories
This category has the following 2 subcategories, out of 2 total.
R
- RASopathies (11 P)
T
Pages in category "Autosomal dominant disorders"
The following 189 pages are in this category, out of 189 total. This list may not reflect recent changes.
A
- Ablepharon macrostomia syndrome
- Acropectoral syndrome
- Acute intermittent porphyria
- Adermatoglyphia
- Albright's hereditary osteodystrophy
- Ankylosing vertebral hyperostosis with tylosis
- Aphalangy-syndactyly-microcephaly syndrome
- Arakawa's syndrome II
- Aromatase excess syndrome
- Autosomal dominant cerebellar ataxia
- Autosomal dominant Charcot-Marie-Tooth disease type 2 with giant axons
- Autosomal dominant GTP cyclohydrolase I deficiency
- Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome
- Autosomal dominant nocturnal frontal lobe epilepsy
- Autosomal dominant partial epilepsy with auditory features
- Autosomal dominant polycystic kidney disease
- Axenfeld–Rieger syndrome
B
- Bainbridge–Ropers syndrome
- Barber–Say syndrome
- Benign hereditary chorea
- Bethlem myopathy
- Birt–Hogg–Dubé syndrome
- Blepharoptosis-myopia-ectopia lentis syndrome
- Boomerang dysplasia
- Bosch-Boonstra-Schaaf optic atrophy syndrome
- Brachydactyly-long thumb syndrome
- Branchio-oto-renal syndrome
- Buschke–Ollendorff syndrome
C
- Calvarial doughnut lesions-bone fragility syndrome
- Camurati–Engelmann disease
- CAPOS syndrome
- Central core disease
- Cerebro-costo-mandibular syndrome
- Cochleosaccular degeneration with progressive cataracts
- Cohen-Gibson syndrome
- Collagen disease
- Collagenopathy, types II and XI
- Collins-Pope syndrome
- Coloboma of macula-brachydactyly type B syndrome
- Congenital distal spinal muscular atrophy
- Congenital stromal corneal dystrophy
- Costello syndrome
- Craniofacial dysostosis-diaphyseal hyperplasia syndrome
- Currarino syndrome
- Cyprus facial neuromusculoskeletal syndrome
- Czech dysplasia, metatarsal type
D
F
G
H
- Hagemoser–Weinstein–Bresnick syndrome
- Hajdu–Cheney syndrome
- Haploinsufficiency of A20
- Hawkinsinuria
- Hay–Wells syndrome
- Heart-hand syndrome, Spanish type
- Helsmoortel-Van der Aa syndrome
- Hemochromatosis type 4
- Hereditary angiopathy with nephropathy, aneurysms, and muscle cramps syndrome
- Hereditary elliptocytosis
- Hereditary hemorrhagic telangiectasia
- Hereditary mucoepithelial dysplasia
- Hereditary neurocutaneous angioma
- Hereditary spherocytosis
- Holt–Oram syndrome
- Huntington's disease
- Huntington's disease-like syndrome
- Hyperinsulinism-hyperammonemia syndrome
- Hypertrophic cardiomyopathy
- Hypoalphalipoproteinemia
- Hypochondroplasia
- Hypodysfibrinogenemia
L
M
- Marfan syndrome
- Marshall syndrome
- Marsili syndrome
- Medullary cystic kidney disease
- Menke-Hennekam syndrome
- Metachondromatosis
- Miller–Dieker syndrome
- MOMO syndrome
- Monilethrix
- MonoMAC
- Multiple endocrine neoplasia
- Multiple endocrine neoplasia type 1
- Multiple endocrine neoplasia type 2
- Multiple endocrine neoplasia type 2B
- Muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome
- Myelokathexis
- Myotonic dystrophy
P
- Pachyonychia congenita
- Pallister–Hall syndrome
- Palmoplantar keratoderma with deafness
- PAPA syndrome
- Papillorenal syndrome
- Parastremmatic dwarfism
- Pelger–Huët anomaly
- Peutz–Jeghers syndrome
- Piebaldism
- Platyspondylic lethal skeletal dysplasia, Torrance type
- Polydactyly
- Polymerase proofreading-associated polyposis
- Popliteal pterygium syndrome
- Porphyria cutanea tarda
- Pseudoachondroplasia
R
S
- Saethre–Chotzen syndrome
- Scalp defects-postaxial polydactyly syndrome
- Schmitt Gillenwater Kelly syndrome
- Severe congenital neutropenia
- Severe intellectual disability-progressive spastic diplegia syndrome
- Short QT syndrome
- Singleton Merten syndrome
- Spastic paraplegia 6
- Spastic paraplegia 31
- Spinal muscular atrophy with lower extremity predominance 1
- Spinal muscular atrophy with lower extremity predominance 2A
- Spinal muscular atrophy with lower extremity predominance 2B
- Spinocerebellar ataxia
- Spinocerebellar ataxia type 1
- Spinocerebellar ataxia type 6
- Split hand split foot-nystagmus syndrome
- Spondyloepimetaphyseal dysplasia, Strudwick type
- Spondyloepiphyseal dysplasia congenita
- Spondyloperipheral dysplasia
- St. Helena familial genu valgum
- Stickler syndrome
- Syndactyly-nystagmus syndrome due to 2q31.1 microduplication
- SYNGAP1-related intellectual disability
- SYT1-associated neurodevelopmental disorder