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Concept information

disease > stomatology > dysmorphic facies > Williams syndrome
... > disease > congenital disease > malformation > dysmorphia > dysmorphic facies > Williams syndrome
disease > developmental disorder > mental retardation > Williams syndrome
disease > disability > mental retardation > Williams syndrome
... > disease > genetic disease > chromosomal aberration > abnormal chromosome > abnormal chromosome C11 > Williams syndrome
disease > congenital disease > malformation > congenital heart disease > Williams syndrome
disease > cardiovascular disease > heart disease > congenital heart disease > Williams syndrome
... > disease > nervous system diseases > neurological disorder > organic mental disorder > cognitive disorder > Williams syndrome

Preferred term

Williams syndrome  

Definition

  • Williams syndrome (WS) is a genetic disorder that affects many parts of the body. Facial features frequently include a broad forehead, short nose and full cheeks, an appearance that has been described as "elfin". (Wikipedia)

Broader concept

Synonym(s)

  • Williams-Beuren syndrome

In other languages

URI

http://data.loterre.fr/ark:/67375/VH8-G4S53RZG-D

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