maffucci syndrome

Preferred Label : maffucci syndrome;

UMLS semantic type : T019 - Congenital Abnormality; T047 - Disease or Syndrome;

Origin ID

M0007381;

UMLS CUI

C0024454;

Automatic exact mappings (from CISMeF team)
- Maffucci syndrome [ICD-11 More detail]
- Maffucci syndrome [MedDRA Preferred Term]
Currated CISMeF NLP mapping
- Enchondromatosis [ICD-10 Sub-category]
- Enchondromatosis [ICD-10 Sub-category (who)]
- Maffucci Syndrome [NCIt concept]
- Maffucci syndrome [PASCAL descriptor]
- Maffucci syndrome [DO Concept]
- Maffucci syndrome [Radlex concept]
- Maffucci syndrome [ORDO Disease]
- Maffucci syndrome (disorder) [SNOMED CT concept]
- Multiple enchondromatosis, maffucci type [OMIM Phenotype]
- maffucci syndrome [SNOMED Notion]
Related record
- enchondromatosis [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Maffucci Syndrome [NCIt concept]
- Maffucci syndrome [ORDO Disease]
- Maffucci syndrome [DO Concept]
- Maffucci syndrome [MedDRA Preferred Term]
- Maffucci syndrome (disorder) [SNOMED CT concept]
- Multiple enchondromatosis, maffucci type [OMIM Phenotype]
- Ollier disease [DO Concept]
- maffucci syndrome [SNOMED Notion]