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Mowat-Wilson syndrome due to monosomy 2q22
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
1 OMIM reference -
1 associated gene
No signs/symptoms info
Mowat-Wilson syndrome due to monosomy 2q22
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

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

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
ZEB2
(0.56)
APP


Citations in the biomedical literature:


Mowat-Wilson syndrome due to monosomy 2q22
ZEB2
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP



Mowat-Wilson syndrome due to monosomy 2q22
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

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):
- HCHWA, Flemish type
Classification (Orphanet):
- Rare abdominal surgical disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
(no data available)
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.