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Scapuloperoneal amyotrophy
1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Desminopathy
1 OMIM reference -
1 associated gene
No signs/symptoms info
Scapuloperoneal amyotrophy
Desminopathy

DES
(UniProt - OMIM)
 DES
(UniProt - OMIM)

COMMON
GENES 		DES


Citations in the biomedical literature:


Scapuloperoneal amyotrophy
DES
Desminopathy



Scapuloperoneal amyotrophy
Desminopathy

Synonym(s):
- Kaeser syndrome
- Neurogenic scapuloperoneal syndrome
- Stark-Kaeser syndrome
Synonym(s):
- Desmin-related myofibrillar myopathy
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.