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Miyoshi myopathy
3 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal dominant limb-girdle muscular dystrophy type 1E
1 associated gene
No signs/symptoms info
Miyoshi myopathy
Autosomal dominant limb-girdle muscular dystrophy type 1E

ANO5
(UniProt - OMIM)
 DES
(UniProt - OMIM)
DYSF
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
DYSF
(0.65)
DES


Citations in the biomedical literature:


Miyoshi myopathy
ANO5 DYSF
Autosomal dominant limb-girdle muscular dystrophy type 1E
DES



Miyoshi myopathy
Autosomal dominant limb-girdle muscular dystrophy type 1E

Synonym(s):
(no synonyms)

Synonym(s):
- LGMD1E
Classification (Orphanet):
- 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:
3 OMIM references -
1 MeSH reference: C537480
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.