Cytoscape Web
Click node...

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

ACTA1
(UniProt - OMIM)
 ETV6
(UniProt - OMIM)
PDGFRB
(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
Chronic myelomonocytic leukemia
ETV6 PDGFRB



Congenital myopathy with excess of thin filaments
Chronic myelomonocytic leukemia

Synonym(s):
- Actin myopathy
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
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: D015477
No signs/symptoms info available.