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Autosomal recessive limb-girdle muscular dystrophy type 2J
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Congenital multicore myopathy with external ophthalmoplegia
1 OMIM reference -
1 associated gene
No signs/symptoms info
Autosomal recessive limb-girdle muscular dystrophy type 2J
Congenital multicore myopathy with external ophthalmoplegia

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

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
TTN
(0.63)
RYR1


Citations in the biomedical literature:


Autosomal recessive limb-girdle muscular dystrophy type 2J
TTN
Congenital multicore myopathy with external ophthalmoplegia
RYR1



Autosomal recessive limb-girdle muscular dystrophy type 2J
Congenital multicore myopathy with external ophthalmoplegia

Synonym(s):
- LGMD2J
Synonym(s):
(no synonyms)
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.