Osteoid osteoma

Preferred Label : Osteoid osteoma;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal recessive vs. viral or other etiology;

Prefixed ID : 259550;

Details

Origin ID

259550;

UMLS CUI

C0029441;

Automatic exact mappings (from CISMeF team)
- Neoplasm musculoskeletal benign/unspecified [ICPC-2 Rubric]
- Osteoid osteoma NOS [ICD-9 code]
Currated CISMeF NLP mapping
- Osteoid Osteoma [NCIt concept]
- Osteoid osteoma [PASCAL descriptor]
- Osteoid osteoma [HPO term]
- Osteoid osteoma [ACR pathology]
- Osteoid osteoma [ACR pathology]
- Osteoid osteoma (disorder) [Inactive SNOMED CT concept]
- Osteoid osteoma (morphologic abnormality) [SNOMED CT concept]
- osteoid osteoma [Radlex concept]
- osteoid osteoma, nos [SNOMED Notion]
- osteoma, osteoid [MeSH Descriptor]
- osteoma, osteoid [MeSH concept]
HPO term(s)
- Abnormality of the skeletal system [HPO term]
- Autosomal recessive inheritance [HPO term]
- Osteoid osteoma [HPO term]
- Osteoma [HPO term]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Osteoid Osteoma [NCIt concept]
- Osteoid osteoma [HPO term]
- Osteoid osteoma (disorder) [Inactive SNOMED CT concept]
- Osteoid osteoma (disorder) [SNOMED CT concept]
- Osteoid osteoma (morphologic abnormality) [SNOMED CT concept]
- osteoid osteoma [Radlex concept]
- osteoid osteoma, nos [SNOMED Notion]
- osteoma, osteoid [MeSH Descriptor]
- osteoma, osteoid [MeSH concept]

Keyword's position in hierarchy(ies) :

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