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Mowat-Wilson syndrome due to a point mutation
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
5 associated genes
No signs/symptoms info
Mowat-Wilson syndrome due to a point mutation
Acute myeloid leukemia with t(8;21)(q22;q22) translocation

ZEB2
(UniProt - OMIM)
 CEBPA
(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)
ZEB2
(0.63)
CEBPA


Citations in the biomedical literature:


Mowat-Wilson syndrome due to a point mutation
ZEB2
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
CEBPA FLT3 KIT RUNX1 RUNX1T1



Mowat-Wilson syndrome due to a point mutation
Acute myeloid leukemia with t(8;21)(q22;q22) translocation

Synonym(s):
- Hirschsprung disease and intellectual deficit due to a point mutation
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare abdominal surgical disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic 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:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.