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Congenital myopathy with excess of thin filaments
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers
1 associated gene
No signs/symptoms info
Congenital myopathy with excess of thin filaments
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers

ACTA1
(UniProt - OMIM)
 DMD
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
ACTA1
(0.87)
DMD


Citations in the biomedical literature:


Congenital myopathy with excess of thin filaments
ACTA1
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers
DMD



Congenital myopathy with excess of thin filaments
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers

Synonym(s):
- Actin myopathy
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare cardiac disease
- 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:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: -
Type of inheritance: x-linked dominant
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.