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Congenital myopathy with excess of thin filaments
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Charcot-Marie-Tooth disease type 4H
1 OMIM reference -
1 associated gene
No signs/symptoms info
Congenital myopathy with excess of thin filaments
Charcot-Marie-Tooth disease type 4H

ACTA1
(UniProt - OMIM)
 FGD4
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
ACTA1
(0.62)
FGD4


Citations in the biomedical literature:


Congenital myopathy with excess of thin filaments
ACTA1
Charcot-Marie-Tooth disease type 4H
FGD4



Congenital myopathy with excess of thin filaments
Charcot-Marie-Tooth disease type 4H

Synonym(s):
- Actin myopathy
Synonym(s):
- CMT4H
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:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.