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Cleidocranial Dysplasia MeSH Descriptor Data 2022


MeSH Heading
Cleidocranial Dysplasia
Tree Number(s)
C05.116.099.708.207
C05.660.207.207
C16.131.621.207.207
Unique ID
D002973
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D002973
Scope Note
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.
Entry Term(s)
Cleidocranial Digital Dysostosis
Cleidocranial Dysostosis
Dysostosis, Cleidocranial
Marie-Sainton Syndrome
Scheuthauer-Marie-Sainton Syndrome
Public MeSH Note
85; was CLEIDOCRANIAL DYSOSTOSIS 1963-84
Online Note
use CLEIDOCRANIAL DYSPLASIA to search CLEIDOCRANIAL DYSOSTOSIS l966-84
History Note
85; was CLEIDOCRANIAL DYSOSTOSIS 1963-84
Date Established
1985/01/01
Date of Entry
1999/01/01
Revision Date
2013/07/08
Cleidocranial Dysplasia Preferred
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