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2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
2 associated genes
No signs/symptoms info
Acute myelomonocytic leukemia
Familial capillary hemangioma

FLT3 ANTXR1
NPM1 KDR


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
NPM1
(0.63)
KDR



Citations in the biomedical literature:


Acute myelomonocytic leukemia
FLT3 NPM1
Familial capillary hemangioma
ANTXR1 KDR



Acute myelomonocytic leukemia
Familial capillary hemangioma

Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare circulatory system disease
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Neoplasms -

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

External references:
No OMIM references
1 MeSH reference: D015479
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.