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Congenital myopathy with excess of thin filaments
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal recessive limb-girdle muscular dystrophy type 2J
1 OMIM reference -
1 associated gene
No signs/symptoms info
Congenital myopathy with excess of thin filaments
Autosomal recessive limb-girdle muscular dystrophy type 2J

ACTA1
(UniProt - OMIM)
 TTN
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
ACTA1
(0.63)
TTN


Citations in the biomedical literature:


Congenital myopathy with excess of thin filaments
ACTA1
Autosomal recessive limb-girdle muscular dystrophy type 2J
TTN



Congenital myopathy with excess of thin filaments
Autosomal recessive limb-girdle muscular dystrophy type 2J

Synonym(s):
- Actin myopathy
Synonym(s):
- LGMD2J
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.