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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
Short stature due to growth hormone qualitative anomaly

FLT3 GH1
KIT
NPM1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
NPM1
(0.63)
GH1



Citations in the biomedical literature:


Acute myeloblastic leukemia with maturation
FLT3 KIT NPM1
Short stature due to growth hormone qualitative anomaly
GH1



Acute myeloblastic leukemia with maturation
Short stature due to growth hormone qualitative anomaly

Synonym(s):
- Acute myeloblastic leukemia type 2

Synonym(s):
- Kowarski syndrome

Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: no data available
Type of inheritance: autosomal recessive

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

No signs/symptoms info available.