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Mowat-Wilson syndrome due to monosomy 2q22
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Acute myeloid leukemia with CEBPA somatic mutations
1 associated gene
No signs/symptoms info
Mowat-Wilson syndrome due to monosomy 2q22
Acute myeloid leukemia with CEBPA somatic mutations

ZEB2
(UniProt - OMIM)
 CEBPA
(UniProt - OMIM)

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


Citations in the biomedical literature:


Mowat-Wilson syndrome due to monosomy 2q22
ZEB2
Acute myeloid leukemia with CEBPA somatic mutations
CEBPA



Mowat-Wilson syndrome due to monosomy 2q22
Acute myeloid leukemia with CEBPA somatic mutations

Synonym(s):
- Hirschsprung disease and intellectual deficit due to 2q22 microdeletion
- Hirschsprung disease and intellectual deficit due to del(2)(q22)
- Hirschsprung disease and intellectual deficit due to monosomy 2q22
- Mowat-Wilson syndrome due to 2q22 microdeletion
- Mowat-Wilson syndrome due to del(2)q(22)
Synonym(s):
- AML with CEBPA somatic mutations
Classification (Orphanet):
- Rare abdominal surgical disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- 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:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.