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

ANTXR1 FLT3
KDR KIT
NPM1


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Familial capillary hemangioma
ANTXR1 KDR
Acute myeloblastic leukemia with maturation
FLT3 KIT NPM1



Familial capillary hemangioma
Acute myeloblastic leukemia with maturation

Synonym(s):
(no synonyms)

Synonym(s):
- Acute myeloblastic leukemia type 2

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

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

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

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

No signs/symptoms info available.