Category:Autosomal dominant disorders
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For more information on autosomal dominant heredity, see the articles Autosome and Dominance (genetics).
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Subcategories
This category has the following 2 subcategories, out of 2 total.
Pages in category "Autosomal dominant disorders"
The following 95 pages are in this category, out of 95 total.
A
- Acrokeratoelastoidosis of Costa
- Acrokeratosis verruciformis
- Acro–dermato–ungual–lacrimal–tooth syndrome
- Acute intermittent porphyria
- Albright's hereditary osteodystrophy
- Atelosteogenesis, type II
- Autosomal dominant cerebellar ataxia
- Autosomal dominant polycystic kidney disease
- Autosomal dominant tubulointerstitial kidney disease due to REN mutations
- Axenfeld–Rieger syndrome
C
D
F
H
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
- Multiple endocrine neoplasia type 1
- 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 1
- Ataxia with Oculomotor Apraxia Type 2
- Spinocerebellar ataxia 28
- Spinocerebellar ataxia 34
- Spinocerebellar ataxia type 1
- Spondyloepimetaphyseal dysplasia Strudwick type
- Spondyloepiphyseal dysplasia congenita
- Swedish mutation
