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Miyoshi myopathy
3 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Congenital muscular dystrophy, Ullrich type
1 OMIM reference -
3 associated genes
No signs/symptoms info
Miyoshi myopathy
Congenital muscular dystrophy, Ullrich type

ANO5
(UniProt - OMIM)
 COL6A1
(UniProt - OMIM)
DYSF
(UniProt - OMIM)
 COL6A2
(UniProt - OMIM)
COL6A3
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
DYSF
(0.63)
COL6A3


Citations in the biomedical literature:


Miyoshi myopathy
ANO5 DYSF
Congenital muscular dystrophy, Ullrich type
COL6A1 COL6A2 COL6A3



Miyoshi myopathy
Congenital muscular dystrophy, Ullrich type

Synonym(s):
(no synonyms)

Synonym(s):
- Scleroatonic muscular dystrophy
- UCMD
- Ullrich disease
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: 1-9 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
External references:
3 OMIM references -
1 MeSH reference: C537480
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.