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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 associated gene
No signs/symptoms info
Acute myeloid leukemia with CEBPA somatic mutations
Mowat-Wilson syndrome due to a point mutation

CEBPA ZEB2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CEBPA
(0.63)
ZEB2



Citations in the biomedical literature:


Acute myeloid leukemia with CEBPA somatic mutations
CEBPA
Mowat-Wilson syndrome due to a point mutation
ZEB2



Acute myeloid leukemia with CEBPA somatic mutations
Mowat-Wilson syndrome due to a point mutation

Synonym(s):
- AML with CEBPA somatic mutations

Synonym(s):
- Hirschsprung disease and intellectual deficit due to a point mutation

Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare abdominal surgical disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic 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:
No OMIM references
No MeSH references

No signs/symptoms info available.