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Cleidocranial Dysplasia

Autosomal dominant syndrome in which there is delayed closing of the CRANIAL FONTANELLES; complete or partial absence of the collarbones (CLAVICLES); wide PUBIC SYMPHYSIS; short middle phalanges of the fifth fingers; and dental and vertebral anomalies.

Year introduced: 1985

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Subheadings:

Tree Number(s): C05.116.099.708.207, C05.660.207.207, C16.131.621.207.207

MeSH Unique ID: D002973

Entry Terms:

  • Cleidocranial Dysplasias
  • Dysplasia, Cleidocranial
  • Dysplasias, Cleidocranial
  • Cleidocranial Digital Dysostosis
  • Cleidocranial Digital Dysostoses
  • Dysostoses, Cleidocranial Digital
  • Dysostosis, Cleidocranial Digital
  • Marie-Sainton Syndrome
  • Marie Sainton Syndrome
  • Syndrome, Marie-Sainton
  • Scheuthauer-Marie-Sainton Syndrome
  • Scheuthauer Marie Sainton Syndrome
  • Syndrome, Scheuthauer-Marie-Sainton
  • Cleidocranial Dysostosis
  • Cleidocranial Dysostoses
  • Dysostoses, Cleidocranial
  • Dysostosis, Cleidocranial

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