×
×
PubCaseFinder
About
Datasets
History
Terms
RDF
API
Contact
EN
/
JA
Mowat-Wilson syndrome
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.
Cleft upper lip
A gap in the upper lip. This is a congenital defect resulting from nonfusion of tissues of the lip during embryonal development.
Total:
0
20
40
60
100
(per page)
PMID (PMCID)