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| Descriptor English: | Camurati-Engelmann Syndrome | ||||||
| Descriptor Spanish: |
Síndrome de Camurati-Engelmann
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| Descriptor Portuguese: | Síndrome de Camurati-Engelmann | ||||||
| Descriptor French: | Syndrome de Camurati-Engelmann | ||||||
| Entry term(s): |
Dysplasie diaphysaire progressive Hyperostose diaphysaire Maladie d'Engelmann Maladie de Camurati-Engelmann |
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| Tree number(s): |
C05.116.099.708.180 C16.320.144 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D003966 | ||||||
| Scope note: | An autosomal dominant form of dysplasia that is characterized by progressive thickening of diaphyseal cortex of long bones. Mutations in the gene that encodes TRANSFORMING GROWTH FACTOR BETA1 are one cause of this disorder. |
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| Allowable Qualifiers: |
BL sang CF liquide cérébrospinal CI induit chimiquement CL classification CO complications DG imagerie diagnostique DH diétothérapie DI diagnostic DT traitement médicamenteux EC économie EH ethnologie EM embryologie EN enzymologie EP épidémiologie ET étiologie GE génétique HI histoire IM immunologie ME métabolisme MI microbiologie MO mortalité NU soins infirmiers PA anatomopathologie PC prévention et contrôle PP physiopathologie PS parasitologie PX psychologie RH rééducation et réadaptation RT radiothérapie SU chirurgie TH thérapie UR urine VE médecine vétérinaire VI virologie |
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| DeCS ID: | 3993 | ||||||
| Unique ID: | D003966 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1991/01/01 | ||||||
| Date of Entry: | 1974/11/11 | ||||||
| Revision Date: | 2018/07/02 |
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Syndrome de Camurati-Engelmann
- Preferred
| Concept UI |
M0006211 |
| Preferred term | Syndrome de Camurati-Engelmann |
| Entry term(s) |
Dysplasie diaphysaire progressive Hyperostose diaphysaire Maladie d'Engelmann Maladie de Camurati-Engelmann |
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