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Summary Literature (0)
DOID:0070067 - White-Sutton syndrome


Disease Ontology Definition:An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of POGZ on chromosome 1q21.3.

Synonyms: MRD37, WHSUS, autosomal dominant mental retardation 37


In Mondo Disease Ontology:
MONDO:0014606 - intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : pogz

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): autosomal dominant non-syndromic intellectual disability (is_a)