Klippel–Feil syndrome (Q1774751)

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Human disease
  • Klippel-Feil syndrome
  • Klippel-Feil and Turner syndrome
  • Klippel-Feil deformity, deafness and facial asymmetry
  • autosomal dominant Klippel-Feil syndrome
  • congenital dystrophia brevicollis
  • congenital synostosis of cervical vertebrae
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Language Label Description Also known as
English
Klippel–Feil syndrome
Human disease
  • Klippel-Feil syndrome
  • Klippel-Feil and Turner syndrome
  • Klippel-Feil deformity, deafness and facial asymmetry
  • autosomal dominant Klippel-Feil syndrome
  • congenital dystrophia brevicollis
  • congenital synostosis of cervical vertebrae

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