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 Dysostosis
- Cleidocranial Dysostoses
- Dysostoses, Cleidocranial
- Dysostosis, Cleidocranial
- Marie-Sainton Syndrome
- Marie Sainton Syndrome
- Syndrome, Marie-Sainton
- Scheuthauer-Marie-Sainton Syndrome
- Scheuthauer Marie Sainton Syndrome
- Syndrome, Scheuthauer-Marie-Sainton
- Cleidocranial Digital Dysostosis
- Cleidocranial Digital Dysostoses
- Dysostoses, Cleidocranial Digital
- Dysostosis, Cleidocranial Digital