Multiple congenital exostoses

Preferred Label : Multiple congenital exostoses;

Inclusion CIM-10 : Diaphyseal aclasis;

Associé à un acte opératoire (%) : 85.0;

Diag associé à un acte (%) : 98.3;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

Q786;

UMLS CUI

C0015306;

Currated CISMeF NLP mapping
- Exostoses, multiple, type I [OMIM Phenotype]
- Multiple congenital exostosis (disorder) [SNOMED CT concept]
- Multiple osteochondromas [ICD-11 Sub-sub category]
- exostoses, multiple hereditary [MeSH Descriptor]
- exostoses, multiple hereditary [MeSH concept]
DO Cross reference
- hereditary multiple exostoses [DO Concept]
Orphanet concepts
- Multiple osteochondromas [ORDO Disease]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Exostoses, multiple, type I [OMIM Phenotype]
- Hereditary Multiple Exostoses [NCIt concept]
- Multiple congenital exostosis (disorder) [SNOMED CT concept]
- Multiple exostoses [HPO term]
- Multiple hereditary exostosis [MedDRA Preferred Term]
- Multiple hereditary exostosis [MedDRA LLT]
- Multiple osteochondromas [ORDO Disease]
- exostoses, multiple hereditary [MeSH Descriptor]
- exostoses, multiple hereditary [MeSH concept]
- hereditary multiple exostoses [Radlex concept]
- hereditary multiple exostoses [DO Concept]
- multiple exostoses syndrome [SNOMED Notion]
- multiple hereditary exostoses [Disease (Nov.)]
- osteochondromatosis [Radlex concept]
- osteochondromatosis syndrome [SNOMED Notion]

Keyword's position in hierarchy(ies) :

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