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.
(previous page) (next page)R
- RASopathies (10 P)
T
Pages in category "Autosomal dominant disorders"
The following 134 pages are in this category, out of approximately 212 total. This list may not reflect recent changes.
(previous page) (next page)G
H
- Hagemoser–Weinstein–Bresnick syndrome
- Hajdu–Cheney syndrome
- Haploinsufficiency of A20
- Hawkinsinuria
- Hay–Wells syndrome
- Heart-hand syndrome, Spanish type
- 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
- Malan syndrome
- 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
N
P
- Pachyonychia congenita
- Pallister–Hall syndrome
- Palmoplantar keratoderma with deafness
- PAPA syndrome
- Papillorenal syndrome
- Parastremmatic dwarfism
- Pashayan syndrome
- 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
- Sack–Barabas syndrome
- 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