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Mowat-Wilson syndrome due to a point mutation
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Mowat-Wilson syndrome due to monosomy 2q22
1 associated gene
No signs/symptoms info
Mowat-Wilson syndrome due to a point mutation
Mowat-Wilson syndrome due to monosomy 2q22

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

COMMON
GENES 		ZEB2


Citations in the biomedical literature:


Mowat-Wilson syndrome due to a point mutation
ZEB2
Mowat-Wilson syndrome due to monosomy 2q22



Mowat-Wilson syndrome due to a point mutation
Mowat-Wilson syndrome due to monosomy 2q22

Synonym(s):
- Hirschsprung disease and intellectual deficit due to a point mutation
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)
Classification (Orphanet):
- Rare abdominal surgical disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare abdominal surgical disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
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.