"Cleidocranial Dysplasia" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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.
| Descriptor ID |
D002973
|
| MeSH Number(s) |
C05.116.099.708.207 C05.660.207.207 C16.131.621.207.207
|
| Concept/Terms |
Cleidocranial Dysplasia- Cleidocranial Dysplasia
- Cleidocranial Dysplasias
- Dysplasia, Cleidocranial
- Dysplasias, Cleidocranial
- Dysostosis, Cleidocranial
- Cleidocranial Digital Dysostosis
- Cleidocranial Digital Dysostoses
- Dysostoses, Cleidocranial Digital
- Dysostosis, Cleidocranial Digital
- Scheuthauer-Marie-Sainton Syndrome
- Scheuthauer Marie Sainton Syndrome
- Syndrome, Scheuthauer-Marie-Sainton
- Cleidocranial Dysostosis
- Cleidocranial Dysostoses
- Dysostoses, Cleidocranial
- Marie-Sainton Syndrome
- Marie Sainton Syndrome
- Syndrome, Marie-Sainton
|
Below are MeSH descriptors whose meaning is more general than "Cleidocranial Dysplasia".
Below are MeSH descriptors whose meaning is more specific than "Cleidocranial Dysplasia".
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Below are the most recent publications written about "Cleidocranial Dysplasia" by people in Profiles.