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

ETV6 ACTA1
PDGFRB CFL2
KLHL41
NEB
TPM2


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
Typical nemaline myopathy
ACTA1 CFL2 KLHL41 NEB TPM2



Chronic myelomonocytic leukemia
Typical 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: 1-9 / 100 000
Average age onset: neonatal/infancy
Average age of death: normal
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.