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2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
3 OMIM references -
4 associated genes
No signs/symptoms info
Chronic myelomonocytic leukemia
Autosomal dominant macrothrombocytopenia

ETV6 ACTN1
PDGFRB ITGA2B
ITGB3
TUBB1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
PDGFRB
(0.74)
ITGB3



Citations in the biomedical literature:


Chronic myelomonocytic leukemia
ETV6 PDGFRB
Autosomal dominant macrothrombocytopenia
ACTN1 ITGA2B ITGB3 TUBB1



Chronic myelomonocytic leukemia
Autosomal dominant macrothrombocytopenia

Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant

External references:
No OMIM references
1 MeSH reference: D015477
External references:
3 OMIM references -
No MeSH references

No signs/symptoms info available.