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Concept information

disease > congenital disease > malformation > Klippel-Feil syndrome
disease > genetic disease > hereditary disease > Klippel-Feil syndrome
disease > congenital disease > malformation > dysostosis > Klippel-Feil syndrome
disease > diseases of the osteoarticular system > dysostosis > Klippel-Feil syndrome
disease > diseases of the osteoarticular system > spine disease > Klippel-Feil syndrome

Preferred term

Klippel-Feil syndrome  

Definition(s)

  • Klippel–Feil syndrome (KFS), also known as cervical vertebral fusion syndrome, is a rare condition present at birth (congenital disease) characterized by the abnormal joining (fusion) of any two of the seven bones in the neck (cervical vertebrae). (Wikipedia)

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URI

http://data.loterre.fr/ark:/67375/VH8-D4VR1G17-D

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RDF/XML TURTLE JSON-LD Last modified 5/14/20