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Congenital myopathy with excess of thin filaments
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Familial isolated restrictive cardiomyopathy
4 OMIM references -
3 associated genes
No signs/symptoms info
Congenital myopathy with excess of thin filaments
Familial isolated restrictive cardiomyopathy

ACTA1
(UniProt - OMIM)
 MYPN
(UniProt - OMIM)
TNNI3
(UniProt - OMIM)
TNNT2
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
ACTA1
(0.52)
TNNI3


Citations in the biomedical literature:


Congenital myopathy with excess of thin filaments
ACTA1
Familial isolated restrictive cardiomyopathy
MYPN TNNI3 TNNT2



Congenital myopathy with excess of thin filaments
Familial isolated restrictive cardiomyopathy

Synonym(s):
- Actin myopathy
Synonym(s):
- Familial or idiopathic restrictive cardiomyopathy
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the circulatory system -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: variable
Average age of death: any age
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
4 OMIM references -
No MeSH references
No signs/symptoms info available.