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Moderate multiminicore disease with hand involvement
1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Congenital multicore myopathy with external ophthalmoplegia
1 OMIM reference -
1 associated gene
No signs/symptoms info
Moderate multiminicore disease with hand involvement
Congenital multicore myopathy with external ophthalmoplegia

RYR1
(UniProt - OMIM)
 RYR1
(UniProt - OMIM)

COMMON
GENES 		RYR1


Citations in the biomedical literature:


Moderate multiminicore disease with hand involvement
RYR1
Congenital multicore myopathy with external ophthalmoplegia



Moderate multiminicore disease with hand involvement
Congenital multicore myopathy with external ophthalmoplegia

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:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.