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Chronic myelomonocytic leukemia
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Intermediate nemaline myopathy
4 associated genes
No signs/symptoms info
Chronic myelomonocytic leukemia
Intermediate nemaline myopathy

ETV6
(UniProt - OMIM)
 ACTA1
(UniProt - OMIM)
PDGFRB
(UniProt - OMIM)
 KLHL41
(UniProt - OMIM)
NEB
(UniProt - OMIM)
TPM3
(UniProt - OMIM)

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


Citations in the biomedical literature:


Chronic myelomonocytic leukemia
ETV6 PDGFRB
Intermediate nemaline myopathy
ACTA1 KLHL41 NEB TPM3



Chronic myelomonocytic leukemia
Intermediate nemaline myopathy

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: any age
Type of inheritance: autosomal dominant
External references:
No OMIM references
1 MeSH reference: D015477
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.