wilson disease

Preferred Label : wilson disease;

MedlinePlus synonym : copper storage disease; hepatolenticular degeneration;

Détails

Origin ID

T1691;

UMLS CUI

C0019202;

Automatic exact mappings (from CISMeF team)
- ATPase copper transporting beta [ORDO Gene]
- ATPase copper transporting beta [HGNC gene]
- congenital anomaly digestive system [ICPC-2 Rubric]
Currated CISMeF NLP mapping
- Disorders of copper metabolism [ICD-10 Sub-category]
- Disorders of copper metabolism [ICD-10 Sub-category (who)]
- Hepato-lenticular degeneration [MedDRA Preferred Term]
- Hepatolenticular Degeneration [NCIt concept]
- Westphal-Strumpell syndrome (disorder) [SNOMED CT concept]
- Wilson disease [PASCAL descriptor]
- Wilson disease [DO Concept]
- Wilson disease [Disease (Nov.)]
- Wilson disease [ICD-11 Sub-sub category]
- Wilson disease [OMIM Phenotype]
- Wilson disease [ORDO Disease]
- Wilson's disease [Blood Transfusion thesaurus concept]
- Wilson's disease [MedDRA LLT]
- Wilson's disease (disorder) [SNOMED CT concept]
- hepatolenticular degeneration [MeSH Descriptor]
- hepatolenticular degeneration [MeSH concept]
- wilson's disease [SNOMED Notion]
MeSH descriptor(s)
- hepatolenticular degeneration [MeSH Descriptor]
See also
- genetic brain disorders [MedlinePlus Topic]
- liver diseases [MedlinePlus Topic]
- metabolic disorders [MedlinePlus Topic]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Cerebral pseudosclerosis (disorder) [SNOMED CT concept]
- Hepato-lenticular degeneration [MedDRA Preferred Term]
- Hepatolenticular Degeneration [NCIt concept]
- Westphal-Strumpell syndrome (disorder) [SNOMED CT concept]
- Wilson disease [OMIM Phenotype]
- Wilson disease [ORDO Disease]
- Wilson disease [DO Concept]
- Wilson disease [PASCAL descriptor]
- Wilson disease [Disease (Nov.)]
- Wilson disease [ICD-11 Sub-sub category]
- Wilson's disease [MedDRA LLT]
- Wilson's disease (disorder) [SNOMED CT concept]
- hepatolenticular degeneration [MeSH concept]
- hepatolenticular degeneration [MeSH Descriptor]
- wilson's disease [SNOMED Notion]
Validated automatic mappings to NTBT
- disorders of copper metabolism [Error of metabolism category]

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