| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| 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://www.omim.org/entry/235730 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the mowat-wilson syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| ZEB2 | zinc finger E-box binding homeobox 2 |
