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Miyoshi myopathy
3 OMIM references -
2 associated genes
No signs/symptoms info
COMMON GENES: 1
Autosomal recessive limb-girdle muscular dystrophy type 2L
1 OMIM reference -
1 associated gene
No signs/symptoms info
Miyoshi myopathy
Autosomal recessive limb-girdle muscular dystrophy type 2L

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

COMMON
GENES 		ANO5


Citations in the biomedical literature:


Miyoshi myopathy
ANO5 DYSF
Autosomal recessive limb-girdle muscular dystrophy type 2L



Miyoshi myopathy
Autosomal recessive limb-girdle muscular dystrophy type 2L

Synonym(s):
(no synonyms)

Synonym(s):
- LGMD2L
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: -
Type of inheritance: autosomal recessive
External references:
3 OMIM references -
1 MeSH reference: C537480
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.