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Summary Literature (0)
DOID:0070054 - Vulto-van Silfout-de Vries syndrome

Disease Ontology Definition:An autosomal dominant intellectual developmental disorder characterized by delayed psychomotor development, poor expressive speech, and behavioral abnormalities that has_material_basis_in an autosomal dominant mutation of the DEAF1 gene on chromosome 11p15.5.

Synonyms: IDDISBAS, MRD24, VSVS, autosomal dominant mental retardation 24, autosomal dominant non-syndromic intellectual disability 24, intellectual developmental disorder with impaired expressive speech and behavioral abnormalities, with or without seizures,

Xenbase Genes : deaf1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014357 - intellectual disability, autosomal dominant 24

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant intellectual developmental disorder (is_a)