osteolysis hereditary multicentric

Preferred Label : osteolysis hereditary multicentric;

MeSH synonym : Torg osteolysis syndrome; Torg-Winchester Syndrome; Torg Syndrome; Multicentric Osteolysis, Nodulosis, and Arthropathy; Nodulosis-Arthropathy-Osteolysis Syndrome; Osteolysis, Hereditary Multicentric; Hereditary multicentric osteolysis; Al-Aqeel Sewairi Syndrome;

Details

Origin ID

C536051;

UMLS CUI

C1850155;

CISMeF manual mappings
- Torg-Winchester syndrome [ORDO Disease]
Currated CISMeF NLP mapping
- Autosomal recessive carpotarsal osteolysis [ORDO Disease]
- Multicentric Osteolysis, Nodulosis, and Arthropathy [NCIt concept]
- Multicentric osteolysis nodulosis arthropathy spectrum (disorder) [SNOMED CT concept]
- Multicentric osteolysis, nodulosis, and arthropathy [OMIM Phenotype]
- Multicentric osteolysis-nodulosis-arthropathy spectrum [ORDO Disease]
- Nodulosis-arthropathy-osteolysis syndrome [ICD-11 More detail]
- Nodulosis-arthropathy-osteolysis syndrome [ORDO Disease]
- Torg-Winchester syndrome [ICD-11 More detail]
- Winchester syndrome (disorder) [SNOMED CT concept]
MeSH term(s) associated for indexing
- osteolysis [MeSH Descriptor]
ORDO relation(s)
- Torg-Winchester syndrome [ORDO Disease]
Record concept(s)
- Osteolysis hereditary multicentric [MeSH concept]
See also inter- (CISMeF)
- Winchester Syndrome [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal recessive carpotarsal osteolysis [ORDO Disease]
- Multicentric Osteolysis, Nodulosis, and Arthropathy [NCIt concept]
- Multicentric osteolysis nodulosis arthropathy spectrum (disorder) [SNOMED CT concept]
- Multicentric osteolysis, nodulosis, and arthropathy [OMIM Phenotype]
- Nodulosis-arthropathy-osteolysis syndrome [ORDO Disease]
- Torg-Winchester syndrome [ORDO Disease]

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