Human genes for Vulto-van Silfout-de Vries syndrome
Vulto-van Silfout-de Vries syndrome [DOID:0070054]
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 DEAF1 on chromosome 11p15.5.
Synonyms: Vulto-van Silfout-de Vries syndrome, DOID:0070054, Vultovan Silfoutde Vries syndrome, Vulto-van Silfout-de Vries disease, Vulto-van Silfout-de Vries disorder ...