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

ACTA1
(UniProt - OMIM)
 CBL
(UniProt - OMIM)
KRAS
(UniProt - OMIM)
NF1
(UniProt - OMIM)
NRAS
(UniProt - OMIM)
PTPN11
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
ACTA1
(0.63)
CBL


Citations in the biomedical literature:


Congenital myopathy with excess of thin filaments
ACTA1
Juvenile myelomonocytic leukemia
CBL KRAS NF1 NRAS PTPN11



Congenital myopathy with excess of thin filaments
Juvenile myelomonocytic leukemia

Synonym(s):
- Actin myopathy
Synonym(s):
- Juvenile chronic myelomonocytic leukemia
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:
1 OMIM reference -
1 MeSH reference: D054429
No signs/symptoms info available.