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Desminopathy
1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Autosomal dominant limb-girdle muscular dystrophy type 1E
1 associated gene
No signs/symptoms info
Desminopathy
Autosomal dominant limb-girdle muscular dystrophy type 1E

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

COMMON
GENES 		DES


Citations in the biomedical literature:


Desminopathy
DES
Autosomal dominant limb-girdle muscular dystrophy type 1E



Desminopathy
Autosomal dominant limb-girdle muscular dystrophy type 1E

Synonym(s):
- Desmin-related myofibrillar myopathy
Synonym(s):
- LGMD1E
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: no data available
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.