Category:Autosomal dominant disorders
From WikiMD's Wellness Encyclopedia
For more information on autosomal dominant heredity, see the articles Autosome and Dominance (genetics).
Subcategories
This category has the following 2 subcategories, out of 2 total.
Pages in category "Autosomal dominant disorders"
The following 121 pages are in this category, out of 121 total.
A
- Ablepharon macrostomia syndrome
- Acropectoral syndrome
- Acute intermittent porphyria
- Adermatoglyphia
- Albright's hereditary osteodystrophy
- Atelosteogenesis, type II
- Autosomal dominant cerebellar ataxia
- Autosomal dominant disorder
- Autosomal dominant disorders
- Autosomal dominant tubulointerstitial kidney disease due to REN mutations
- Axenfeld–Rieger syndrome
B
C
D
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
- Pyogenic arthritis, pyoderma gangrenosum and acne
- Pelger–Huët anomaly
- Peutz-Jeghers syndrome
- Platyspondylic lethal skeletal dysplasia Torrance type
- Polycystic kidney disease, adult type
- Polycystic kidney disease, type 1
- Polycystic kidney disease, type 2
- Polydactyly
- Popliteal pterygium syndrome
- Porphyria cutanea tarda
- Primrose syndrome
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
