D002973Level 6
Cleidocranial Dysplasia
**Definition:** 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.
**Tree numbers:** - C05.116.099.708.207 - C05.660.207.207 - C16.131.621.207.207
**Synonyms:** - Cleidocranial Dysostosis - Dysostosis, Cleidocranial - Marie-Sainton Syndrome - Scheuthauer-Marie-Sainton Syndrome - Cleidocranial Digital Dysostosis
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