Summary Literature (0)

DOID:0070067 - White-Sutton syndrome

Disease Ontology Definition:An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the POGZ gene on chromosome 1q21.3.

Synonyms: autosomal dominant mental retardation 37, MRD37, WHSUS

Xenbase Genes : pogz

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014606 - intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome

MIM:

MIM:616364 - WHITE-SUTTON SYNDROME; WHSUS

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee