genochondromatosis

Preferred Label : genochondromatosis;

Origin ID

C563215;

UMLS CUI

C1300229;

Automatic exact mappings (from CISMeF team)
- Genochondromatosis [ICD-11 More detail]
Currated CISMeF NLP mapping
- Genochondromatosis [OMIM Phenotype]
- Genochondromatosis (disorder) [SNOMED CT concept]
- Genochondromatosis type 1 [ORDO Disease]
MeSH term(s) associated for indexing
- bone neoplasms [MeSH Descriptor]
- chondromatosis [MeSH Descriptor]
- neoplastic syndromes, hereditary [MeSH Descriptor]
Record concept(s)
- genochondromatosis [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Genochondromatosis [OMIM Phenotype]
- Genochondromatosis (disorder) [SNOMED CT concept]
- Genochondromatosis type 1 [ORDO Disease]
Validated automatic mappings to BTNT
- Genochondromatosis type 1 (disorder) [SNOMED CT concept]