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Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
4 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 myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
Familial platelet syndrome with predisposition to acute myelogenous leukemia

CBFB
(UniProt - OMIM)
 RUNX1
(UniProt - OMIM)
FLT3
(UniProt - OMIM)
KIT
(UniProt - OMIM)
MYH11
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
CBFB
(0.99)
RUNX1


Citations in the biomedical literature:


Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
CBFB FLT3 KIT MYH11
Familial platelet syndrome with predisposition to acute myelogenous leukemia
RUNX1



Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
Familial platelet syndrome with predisposition to acute myelogenous leukemia

Synonym(s):
(no synonyms)

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.