Structured Summary
Abstract
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.
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Classification
Broader headings
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MeSH Record
Synonyms
17 entry terms
- Cleidocranial Digital Dysostosis
- Cleidocranial Dysostosis
- Dysostosis, Cleidocranial
- Marie-Sainton Syndrome
- Scheuthauer-Marie-Sainton Syndrome
- Cleidocranial Digital Dysostoses
- Cleidocranial Dysostoses
- Cleidocranial Dysplasias
- Dysostoses, Cleidocranial
- Dysostoses, Cleidocranial Digital
- Dysostosis, Cleidocranial Digital
- Dysplasia, Cleidocranial
- Dysplasias, Cleidocranial
- Marie Sainton Syndrome
- Scheuthauer Marie Sainton Syndrome
- Syndrome, Marie-Sainton
- Syndrome, Scheuthauer-Marie-Sainton
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
History Note
85; was CLEIDOCRANIAL DYSOSTOSIS 1963-84
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References
- National Library of Medicine. Cleidocranial Dysplasia. Medical Subject Headings (MeSH). 2026. Unique ID D002973. http://id.nlm.nih.gov/mesh/2026/D002973
- Cleidocranial Dysplasia. In: Wikipedia. https://en.wikipedia.org/wiki/Cleidocranial_dysostosis
- Cleidocranial Dysplasia. In: Wikidata. https://www.wikidata.org/wiki/Q781618