Cytoscape Web
Click node...

Acute megakaryoblastic leukemia without Down syndrome
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Familial platelet syndrome with predisposition to acute myelogenous leukemia
1 OMIM reference -
1 associated gene
No signs/symptoms info
Acute megakaryoblastic leukemia without Down syndrome
Familial platelet syndrome with predisposition to acute myelogenous leukemia

CBFA2T3
(UniProt - OMIM)
 RUNX1
(UniProt - OMIM)
GLIS2
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
CBFA2T3
(0.75)
RUNX1


Citations in the biomedical literature:


Acute megakaryoblastic leukemia without Down syndrome
CBFA2T3 GLIS2
Familial platelet syndrome with predisposition to acute myelogenous leukemia
RUNX1



Acute megakaryoblastic leukemia without Down syndrome
Familial platelet syndrome with predisposition to acute myelogenous leukemia

Synonym(s):
- Non-DS-AMKL
Synonym(s):
- FPD/AML syndrome
- FPS/AML syndrome
- Familial platelet disorder with associated myeloid malignancy
- Familial platelet syndrome
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
- Rare oncologic 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: no data available
Average age of death: no data available
Type of inheritance: autosomal dominant
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.