Mowat-Wilson syndrome Gene Set

Dataset ClinVar Gene-Phenotype 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
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Genes

1 genes associated with the Mowat-Wilson syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
ZEB2 zinc finger E-box binding homeobox 2