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

ACTN1
(UniProt - OMIM)
 ETV6
(UniProt - OMIM)
ITGA2B
(UniProt - OMIM)
 PDGFRB
(UniProt - OMIM)
ITGB3
(UniProt - OMIM)
TUBB1
(UniProt - OMIM)

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


Citations in the biomedical literature:


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



Autosomal dominant macrothrombocytopenia
Chronic myelomonocytic leukemia

Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Neoplasms -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
3 OMIM references -
No MeSH references
External references:
No OMIM references
1 MeSH reference: D015477
No signs/symptoms info available.