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Congenital myopathy, Paradas type
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Rippling muscle disease
2 OMIM references -
1 associated gene
No signs/symptoms info
Congenital myopathy, Paradas type
Rippling muscle disease

DYSF
(UniProt - OMIM)
 CAV3
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
DYSF
(0.74)
CAV3


Citations in the biomedical literature:


Congenital myopathy, Paradas type
DYSF
Rippling muscle disease
CAV3



Congenital myopathy, Paradas type
Rippling muscle 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:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
2 OMIM references -
1 MeSH reference: C535685
No signs/symptoms info available.