Concept information
Terme préférentiel
Williams syndrome
Définition
- Williams syndrome (WS) is a neurodevelopmental disorder caused by the deletion of some 28 genes on one copy of Chromosome 7. The deletion gives rise to distinctive facial features and affects the developing body, brain, mind, and behavior. [Source: Encyclopedia of the Mind; Williams Syndrome]
Concept générique
Appartient au groupe
URI
http://data.loterre.fr/ark:/67375/N9J-QF8TL4H6-M
{{label}}
{{#each values }} {{! loop through ConceptPropertyValue objects }}
{{#if prefLabel }}
{{/if}}
{{/each}}
{{#if notation }}{{ notation }} {{/if}}{{ prefLabel }}
{{#ifDifferentLabelLang lang }} ({{ lang }}){{/ifDifferentLabelLang}}
{{#if vocabName }}
{{ vocabName }}
{{/if}}