chordoma - CISMeF

Preferred Label : chordoma;

Origin ID

M-93703;

UMLS CUI

C0008487;

Currated CISMeF NLP mapping
- Chordoma [PASCAL descriptor]
- Chordoma [ICD-11 More detail]
- Chordoma [ICD-9 code]
- Chordoma [ACR pathology]
- Chordoma [NCIt concept]
- Chordoma [MedDRA Preferred Term]
- Chordoma [HPO term]
- Chordoma [ORDO Disease]
- Chordoma (disorder) [SNOMED CT concept]
- Chordoma (morphologic abnormality) [SNOMED CT concept]
- Chordoma, NOS [ICD-O code]
- Chordoma, susceptibility to [OMIM Phenotype]
- chordoma [Radlex concept]
- chordoma [DO Concept]
- chordoma [Disease (Nov.)]
- chordoma [MeSH Descriptor]
- chordoma [MeSH concept]
Manual NTBT mappings (CISMeF)
- Genetic bone tumor [ORDO Disease]
- Pituitary hormone deficiency of tumoral origin [ORDO Disease]
- Rare bone tumor [ORDO Disease]
- Rare genetic tumor [ORDO Disease]
SNOMED CT concept
- Chordoma (morphologic abnormality) [SNOMED CT concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Chordoma [ORDO Disease]
- Chordoma [HPO term]
- Chordoma [PASCAL descriptor]
- Chordoma [MedDRA Preferred Term]
- Chordoma [NCIt concept]
- Chordoma (disorder) [SNOMED CT concept]
- Chordoma (morphologic abnormality) [SNOMED CT concept]
- Chordoma, NOS [ICD-O code]
- Chordoma, susceptibility to [OMIM Phenotype]
- chordoma [MeSH concept]
- chordoma [Disease (Nov.)]
- chordoma [DO Concept]
- chordoma [Radlex concept]
- chordoma [MeSH Descriptor]