| Descriptor English: | Cleidocranial Dysplasia | ||||||
| Descriptor Spanish: |
Displasia Cleidocraneal
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| Descriptor Portuguese: | Displasia Cleidocraniana | ||||||
| Descriptor French: | Dysostose cleido-crânienne héréditaire | ||||||
| Entry term(s): |
Cleidocranial Digital Dysostoses Cleidocranial Digital Dysostosis Cleidocranial Dysostoses Cleidocranial Dysostosis Cleidocranial Dysplasias Dysostoses, Cleidocranial Dysostoses, Cleidocranial Digital Dysostosis, Cleidocranial Dysostosis, Cleidocranial Digital Dysplasia, Cleidocranial Dysplasias, Cleidocranial Marie Sainton Syndrome Marie-Sainton Syndrome Scheuthauer Marie Sainton Syndrome Scheuthauer-Marie-Sainton Syndrome Syndrome, Marie-Sainton Syndrome, Scheuthauer-Marie-Sainton |
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| Tree number(s): |
C05.116.099.708.207 C05.660.207.207 C16.131.621.207.207 |
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| RDF Unique Identifier: | https://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. |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Public MeSH Note: | 85; was CLEIDOCRANIAL DYSOSTOSIS 1963-84 |
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| Online Note: | use CLEIDOCRANIAL DYSPLASIA to search CLEIDOCRANIAL DYSOSTOSIS l966-84 |
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| History Note: | 85; was CLEIDOCRANIAL DYSOSTOSIS 1963-84 |
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| DeCS ID: | 2998 | ||||||
| Unique ID: | D002973 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1985/01/01 | ||||||
| Date of Entry: | 1999/01/01 | ||||||
| Revision Date: | 2013/07/08 |
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Cleidocranial Dysplasia
- Preferred
| Concept UI |
M0004550 |
| 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. |
| Preferred term | Cleidocranial Dysplasia |
| Entry term(s) |
Cleidocranial Digital Dysostoses Cleidocranial Digital Dysostosis Cleidocranial Dysostoses Cleidocranial Dysostosis Cleidocranial Dysplasias Dysostoses, Cleidocranial Dysostoses, Cleidocranial Digital Dysostosis, Cleidocranial Dysostosis, Cleidocranial Digital Dysplasia, Cleidocranial Dysplasias, Cleidocranial Marie Sainton Syndrome Marie-Sainton Syndrome Scheuthauer Marie Sainton Syndrome Scheuthauer-Marie-Sainton Syndrome Syndrome, Marie-Sainton Syndrome, Scheuthauer-Marie-Sainton |
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