Category:Autosomal dominant disorders
From WikiMD's Food, Medicine & Wellness Encyclopedia
For more information on autosomal dominant heredity, see the articles Autosome and Dominance (genetics).
Pages in category "Autosomal dominant disorders"
The following 120 pages are in this category, out of 120 total.
A
- Ablepharon macrostomia syndrome
- Acropectoral syndrome
- Acute intermittent porphyria
- Adermatoglyphia
- Albright's hereditary osteodystrophy
- Aromatase excess syndrome
- Atelosteogenesis, type II
- Autosomal dominant cerebellar ataxia
- Autosomal dominant disorders
- Autosomal dominant tubulointerstitial kidney disease due to REN mutations
- Axenfeld–Rieger syndrome
B
C
D
F
H
- Hajdu-Cheney syndrome
- Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome
- Hereditary elliptocytosis
- Hereditary hemorrhagic telangiectasia
- Hereditary mucoepithelial dysplasia
- Hereditary spherocytosis
- Holt–Oram syndrome
- Huntington's disease
- Familial hypertrophic cardiomyopathy
- Hypodysfibrinogenemia
- Hystrix-like ichthyosis–deafness syndrome
M
- Machado–Joseph disease
- Marfan syndrome
- Autosomal dominant tubulointerstitial kidney disease
- Autosomal dominant tubulointerstitial kidney disease due to MUC1 mutations
- Autosomal dominant tubulointerstitial kidney disease due to UMOD mutations
- Metachondromatosis
- Monilethrix
- Multiple endocrine adenomatosis
- Multiple endocrine neoplasia type 1
- Multiple endocrine neoplasia type 2b
- Multiple endocrine neoplasia type 2B
- Myotonic dystrophy
- Myotonic dystrophy type 1
- Myotonic dystrophy type 2
P
S
- Shprintzen–Goldberg syndrome
- Singleton-Merten syndrome
- Spinal muscular atrophy with lower extremity predominance
- Ataxia with Oculomotor Apraxia Type 2
- Infantile onset spinocerebellar ataxia
- Spinocerebellar ataxia 28
- Spinocerebellar ataxia 34
- Spinocerebellar ataxia type 1
- Spondyloepimetaphyseal dysplasia Strudwick type
- Spondyloepiphyseal dysplasia congenita
