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Congenital myopathy with excess of thin filaments
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Progressive sensorineural hearing loss - hypertrophic cardiomyopathy
1 OMIM reference -
1 associated gene
No signs/symptoms info
Congenital myopathy with excess of thin filaments
Progressive sensorineural hearing loss - hypertrophic cardiomyopathy

ACTA1
(UniProt - OMIM)
 MYO6
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
ACTA1
(0.52)
MYO6


Citations in the biomedical literature:


Congenital myopathy with excess of thin filaments
ACTA1
Progressive sensorineural hearing loss - hypertrophic cardiomyopathy
MYO6



Congenital myopathy with excess of thin filaments
Progressive sensorineural hearing loss - hypertrophic cardiomyopathy

Synonym(s):
- Actin myopathy
Synonym(s):
- Progressive neurosensory deafness - hypertrophic cardiomyopathy
- Progressive neurosensory hearing loss - hypertrophic cardiomyopathy
- Progressive sensorineural deafness - hypertrophic cardiomyopathy
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare cardiac disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare otorhinolaryngologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.