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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
Isolated growth hormone deficiency type IA

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
Isolated growth hormone deficiency type IA
GH1



Acute myeloblastic leukemia with maturation
Isolated growth hormone deficiency type IA

Synonym(s):
- Acute myeloblastic leukemia type 2

Synonym(s):
- Congenital IGHD type IA
- Congenital isolated GH deficiency type IA
- Congenital isolated growth hormone deficiency type IA

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: -
Average age onset: neonatal/infancy
Average age of death: -
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.