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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
2 associated genes
No signs/symptoms info
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Acute myeloblastic leukemia without maturation

CBL FLT3
NPM1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CBL
(0.68)
FLT3



Citations in the biomedical literature:


Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
CBL
Acute myeloblastic leukemia without maturation
FLT3 NPM1



Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Acute myeloblastic leukemia without maturation

Synonym(s):
- CBL syndrome
- Noonan syndrome-like disorder with JMML

Synonym(s):
- Acute myeloblastic leukemia type 1

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

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