Cytoscape Web
Click node...

Congenital myopathy with excess of thin filaments
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Congenital mesoblastic nephroma
2 associated genes
No signs/symptoms info
Congenital myopathy with excess of thin filaments
Congenital mesoblastic nephroma

ACTA1
(UniProt - OMIM)
 ETV6
(UniProt - OMIM)
NTRK3
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
ACTA1
(0.55)
ETV6


Citations in the biomedical literature:


Congenital myopathy with excess of thin filaments
ACTA1
Congenital mesoblastic nephroma
ETV6 NTRK3



Congenital myopathy with excess of thin filaments
Congenital mesoblastic nephroma

Synonym(s):
- Actin myopathy
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
(no data available)
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Neoplasms -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
1 MeSH reference: D018201
No signs/symptoms info available.