| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | Mowat-Wilson syndrome (MWS) is a multiple congenital anomaly syndrome characterized by a distinct facial phenotype, intellectual disability, epilepsy, Hirschsprung disease (HSCR; see this term) and variable congenital malformations. (Orphanet Rare Disease Ontology, Orphanet_2152) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:C536990 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Mowat-Wilson syndrome from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| ZEB2 | zinc finger E-box binding homeobox 2 | 2.88009 |
