Klippel-Feil syndrome (Q1774751)

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physical disorder that has material basis in abnormal segmentation of the vertebra during fetal development which results in fusion located in cervical vertebra
  • 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
  • Cervical vertebral fusion
  • Klippel Feil syndrome
  • Klippel–Feil syndrome
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Language Label Description Also known as
English
Klippel-Feil syndrome
physical disorder that has material basis in abnormal segmentation of the vertebra during fetal development which results in fusion located in cervical vertebra
  • 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
  • Cervical vertebral fusion
  • Klippel Feil syndrome
  • Klippel–Feil syndrome

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Klippel.JPG
421 × 607; 39 KB
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Klippel–Feil syndrome
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Identifiers

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LB73.20
Klippel-Feil anomaly
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