has material basis in germline mutation in POGZ congenital nervous system disorder intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome https://github.com/monarch-initiative/mondo/issues/5588 https://github.com/monarch-initiative/mondo/issues/7964 https://www.malacards.org/card/white_sutton_syndrome Orphanet:468678 intellectual disability, autosomal dominant 37 mental retardation, autosomal dominant type 37 MRD37 mental retardation, autosomal dominant 37 MEDGEN:897984 intellectual disability, autosomal dominant type 37 intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome Intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome is a rare, genetic, syndromic intellectual disability disorder characterized by craniofacial dysmorphism (microcephaly, hypotonic facies, strabismus, long and flat malar region, posteriorly rotated ears, flat nasal bridge with broad nasal tip, short philtrum, thin vermillion border, open mouth with down-turned corners, high arched palate, pointed chin), global developmental delay, intellectual disability and variable neurobehavioral abnormalities (autism spectrum disorder, aggressiveness, self injury). Additional features include vision abnormalities and variable sensorineural hearing loss, as well as short stature, hypotonia and gastrointestinal manifestations (e.g. poor feeding, gastroesophageal reflux, constipation). autosomal dominant intellectual disability 37 OMIM:616364 GARD:0013774 DOID:0070067 MONDO:0014606 UMLS:C4225351 WHSUS multiple congenital anomalies/dysmorphic syndrome-intellectual disability autosomal dominant non-syndromic intellectual disability autosomal dominant syndromic intellectual disability