tangier disease

Preferred Label : tangier disease;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0021031;

UMLS CUI

C0039292;

Automatic exact mappings (from CISMeF team)
- ATP binding cassette subfamily A member 1 [ORDO Gene]
- ATP binding cassette subfamily A member 1 [HGNC gene]
- Analphalipoproteinaemia [ICD-11 More detail]
- Hypoalphalipoproteinemia [PASCAL descriptor]
- Lipoprotein deficiency [ICD-10 Sub-category]
- Lipoprotein deficiency [ICD-10 Sub-category (who)]
Currated CISMeF NLP mapping
- Familial hypoalphalipoproteinemia (disorder) [SNOMED CT concept]
- Hypoalphalipoproteinemia, primary, 1 [OMIM Phenotype]
- Tangier Disease [NCIt concept]
- Tangier disease [DO Concept]
- Tangier disease [Disease (Nov.)]
- Tangier disease [MedDRA Preferred Term]
- Tangier disease [OMIM Phenotype]
- Tangier disease [ORDO Disease]
- Tangier disease (disorder) [SNOMED CT concept]
- familial hypoalphalipoproteinemia [SNOMED Notion]
MeSH narrower concept(s)
- tangier disease neuropathy [MeSH concept]
Related record
- tangier disease [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Tangier Disease [NCIt concept]
- Tangier disease [ORDO Disease]
- Tangier disease [OMIM Phenotype]
- Tangier disease [MedDRA Preferred Term]
- Tangier disease [DO Concept]
- Tangier disease (disorder) [SNOMED CT concept]