exostoses, multiple hereditary

Preferred Label : exostoses, multiple hereditary;

UMLS semantic type : T019 - Congenital Abnormality; T191 - Neoplastic Process;

Details

Origin ID

M0008037;

UMLS CUI

C0015306;

Currated CISMeF NLP mapping
- Exostoses, multiple, type I [OMIM Phenotype]
- Hereditary Multiple Exostoses [NCIt concept]
- Multiple Osteochondromas [NCIt concept]
- Multiple cartilaginous exostosis [PASCAL descriptor]
- Multiple congenital exostoses [ICD-10 Sub-category]
- Multiple congenital exostoses [ICD-10 Sub-category (who)]
- Multiple congenital exostosis (disorder) [SNOMED CT concept]
- Multiple exostoses [HPO term]
- Multiple hereditary exostosis [MedDRA Preferred Term]
- Multiple osteochondromas [ORDO Disease]
- hereditary multiple exostoses [DO Concept]
- hereditary multiple exostoses [Radlex concept]
- multiple exostoses syndrome [SNOMED Notion]
- multiple hereditary exostoses [Disease (Nov.)]
Related record
- exostoses, multiple hereditary [MeSH Descriptor]
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 exostoses [ICD-10 Sub-category]
- 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]
- hereditary multiple exostoses [DO Concept]
- hereditary multiple exostoses [Radlex 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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