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Miyoshi myopathy
3 OMIM references -
2 associated genes
No signs/symptoms info
COMMON GENES: 1
Congenital myopathy, Paradas type
1 associated gene
No signs/symptoms info
Miyoshi myopathy
Congenital myopathy, Paradas type

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

COMMON
GENES 		DYSF


Citations in the biomedical literature:


Miyoshi myopathy
ANO5 DYSF
Congenital myopathy, Paradas type



Miyoshi myopathy
Congenital myopathy, Paradas type

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:
(no data available)
External references:
3 OMIM references -
1 MeSH reference: C537480
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.