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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Pages in category "Autosomal dominant disorders"
The following 104 pages are in this category, out of 104 total.
A
B
C
G
H
- Hajdu–Cheney syndrome
- Hawkinsinuria
- Hay–Wells syndrome
- Hemochromatosis type 4
- Hereditary amyloidosis transthyretin-related
- Hereditary elliptocytosis
- Hereditary hemorrhagic telangiectasia
- Hereditary mucoepithelial dysplasia
- Hereditary spherocytosis
- Holt–Oram syndrome
- Huntington's disease
- Hypertrophic cardiomyopathy
- Hypochondroplasia
M
P
S
- Saethre–Chotzen syndrome
- Severe congenital neutropenia
- Short QT syndrome
- Spastic paraplegia 31
- Spinal muscular atrophy with lower extremity predominance 1
- Spinal muscular atrophy with lower extremity predominance 2A
- 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
- Stickler syndrome