bn:00081236n
Noun Concept
Categories: Rare syndromes, Autosomal monosomies and deletions, Syndromes with craniofacial abnormalities, Syndromes affecting the heart, Syndromes
EN
Williams syndrome  Williams-Beuren syndrome  Williams's syndrome  Williams Disease  William’s Syndrome
EN
A rare congenital disorder associated with deletion of genetic material in chromosome 7; characterized by mental deficiency and some growth deficiency and elfin faces but an overly social personality and a remarkable gift for vocabulary WordNet 3.0
Definitions
Relations
Sources
EN
A rare congenital disorder associated with deletion of genetic material in chromosome 7; characterized by mental deficiency and some growth deficiency and elfin faces but an overly social personality and a remarkable gift for vocabulary WordNet 3.0 & Open English WordNet
Williams syndrome, also Williams–Beuren syndrome, is a genetic disorder that affects many parts of the body. Wikipedia
A developmental disorder known for its distinctive "elfin" facial features Wikipedia Disambiguation
Neurodevelopmental disorder Wikidata
A rare neurodevelopmental disorder characterized by a distinctive elfin facial appearance, developmental delay coupled with strong language skills, and cardiovascular problems. Wiktionary
A rare neurodevelopmental disorder. Wiktionary (translation)