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Acute myeloid leukemia with t(8;21)(q22;q22) translocation
5 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
1 OMIM reference -
1 associated gene
No signs/symptoms info
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia

CEBPA
(UniProt - OMIM)
 CBL
(UniProt - OMIM)
FLT3
(UniProt - OMIM)
KIT
(UniProt - OMIM)
RUNX1
(UniProt - OMIM)
RUNX1T1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
KIT
FLT3
(0.75)
(0.68)
CBL
CBL


Citations in the biomedical literature:


Acute myeloid leukemia with t(8;21)(q22;q22) translocation
CEBPA FLT3 KIT RUNX1 RUNX1T1
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
CBL



Acute myeloid leukemia with t(8;21)(q22;q22) translocation
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
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.