has material basis in germline mutation in ZEB2 congenital nervous system disorder Mowat-Wilson syndrome https://rarediseases.info.nih.gov/diseases/9673/mowat-wilson-syndrome https://www.malacards.org/card/mowat_wilson_syndrome NANDO:2200981 GARD:0009673 NORD:1456 microcephaly, intellectual disability, and distinct facial featrues, with or without Hirschprung disease MEDGEN:341067 Mowat-Wilson syndrome (MWS) is a multiple congenital anomaly syndrome characterized by a distinct facial phenotype, intellectual disability, epilepsy, Hirschsprung disease (HSCR) and variable congenital malformations. NANDO:1200663 Orphanet:2152 icd11.foundation:1985672762 ICD9:759.89 Mowat-Wilson syndrome UMLS:C1856113 Hirschsprung disease-intellectual disability syndrome mental retardation, microcephaly, and distinct facial features with or without Hirschsprung disease Hirschsprung disease-mental retardation syndrome DOID:0060485 NCIT:C74999 MONDO:0009341 OMIM:235730 Hirschsprung disease intellectual disability syndrome intellectual disability, microcephaly, and distinct facial features with or without Hirschsprung disease MOWS MESH:C536990 microcephaly, mental retardation, and distinct Facial features, with or without Hirschsprung disease SCTID:703535000 multiple congenital anomalies/dysmorphic syndrome-intellectual disability monogenic epilepsy autosomal dominant syndromic intellectual disability