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Acute myelomonocytic leukemia
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hereditary site-specific ovarian cancer syndrome
2 associated genes
No signs/symptoms info
Acute myelomonocytic leukemia
Hereditary site-specific ovarian cancer syndrome

FLT3
(UniProt - OMIM)
 BRCA1
(UniProt - OMIM)
NPM1
(UniProt - OMIM)
 BRCA2
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
NPM1
(0.79)
BRCA1


Citations in the biomedical literature:


Acute myelomonocytic leukemia
FLT3 NPM1
Hereditary site-specific ovarian cancer syndrome
BRCA1 BRCA2



Acute myelomonocytic leukemia
Hereditary site-specific ovarian cancer syndrome

Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare gynecologic or obstetric disease
- Rare oncologic disease
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Neoplasms -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
No OMIM references
1 MeSH reference: D015479
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.