Cytoscape Web
Click node...

Acute biphenotypic leukemia
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
1 OMIM reference -
1 associated gene
No signs/symptoms info
Acute biphenotypic leukemia
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia

FLT3
(UniProt - OMIM)
 CBL
(UniProt - OMIM)
KMT2A
(UniProt - OMIM)

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


Citations in the biomedical literature:


Acute biphenotypic leukemia
FLT3 KMT2A
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
CBL



Acute biphenotypic leukemia
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia

Synonym(s):
(no synonyms)

Synonym(s):
- CBL syndrome
- Noonan syndrome-like disorder with JMML
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare cardiac disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare oncologic disease
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
No OMIM references
1 MeSH reference: D015456
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.