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3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Acute myeloblastic leukemia with maturation
Congenital valvular dysplasia

FLT3 FLNA
KIT
NPM1


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Acute myeloblastic leukemia with maturation
FLT3 KIT NPM1
Congenital valvular dysplasia
FLNA



Acute myeloblastic leukemia with maturation
Congenital valvular dysplasia

Synonym(s):
- Acute myeloblastic leukemia type 2

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare surgical cardiac disease

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: sporadic

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

No signs/symptoms info available.