Williams-Beuren syndrome

Summary

DOID:1928 - Williams-Beuren syndrome

Disease Ontology Definition:A syndrome that is characterized by mild to moderate intellectual disability, a broad forehead, a short nose with a broad tip, full cheeks, and a wide mouth with full lips and difficulty with visual-spatial tasks and has_material_basis_in hemizygous deletion of 1.5 to 1.8 Mb on chromosome 7q11.23.

Synonyms: Fanconi Schlesinger syndrome, WBS,

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: mlxipl, gtf2i, gtf2ird1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0008678 - Williams syndrome

MONDO:0008678 - Williams syndrome

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

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

Parent(s): autosomal dominant disease (is_a), chromosomal deletion syndrome (is_a), syndrome (is_a)