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Juvenile myelomonocytic leukemia
1 OMIM reference -
5 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hereditary inclusion body myopathy - joint contractures - ophthalmoplegia
1 OMIM reference -
1 associated gene
No signs/symptoms info
Juvenile myelomonocytic leukemia
Hereditary inclusion body myopathy - joint contractures - ophthalmoplegia

CBL
(UniProt - OMIM)
 MYH2
(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)
CBL
(0.63)
MYH2


Citations in the biomedical literature:


Juvenile myelomonocytic leukemia
CBL KRAS NF1 NRAS PTPN11
Hereditary inclusion body myopathy - joint contractures - ophthalmoplegia
MYH2



Juvenile myelomonocytic leukemia
Hereditary inclusion body myopathy - joint contractures - ophthalmoplegia

Synonym(s):
- Juvenile chronic myelomonocytic leukemia
Synonym(s):
- HIBM3
- Hereditary inclusion body myopathy type 3
- IBM3
- Inclusion body myopathy type 3
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Neoplasms -
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 dominant
External references:
1 OMIM reference -
1 MeSH reference: D054429
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.