Hypoalphalipoproteinemia

Preferred Label : Hypoalphalipoproteinemia;

NCIt definition : A metabolic disorder characterized by deficiency of high density (alpha) lipoprotein in the blood.;

Details

Origin ID

C84774;

UMLS CUI

C0473527;

Automatic exact mappings (from CISMeF team)
- Decreased HDL cholesterol concentration [HPO term]
- Hypoalphalipoproteinaemia [ICD-11 Subcategory]
- Hypoalphalipoproteinemia [PASCAL descriptor]
- Lipoprotein deficiency [ICD-10 Sub-category (who)]
- Lipoprotein deficiency [ICD-10 Sub-category]
Currated CISMeF NLP mapping
- Hypoalphalipoproteinaemia [MedDRA LLT]
- Hypoalphalipoproteinemia [ORDO Disease]
- Hypoalphalipoproteinemia [MedDRA LLT]
- Hypoalphalipoproteinemia (disorder) [SNOMED CT concept]
- Hypoalphalipoproteinemia, primary, 1 [OMIM Phenotype]
- hypoalphalipoproteinemias [MeSH Descriptor]
- hypoalphalipoproteinemias [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- High density lipoid deficiency (disorder) [Inactive SNOMED CT concept]
- Hypoalphalipoproteinaemia [MedDRA LLT]
- Hypoalphalipoproteinemia [ORDO Disease]
- Hypoalphalipoproteinemia [MedDRA LLT]
- Hypoalphalipoproteinemia (disorder) [SNOMED CT concept]
- hypoalphalipoproteinemias [MeSH concept]
- hypoalphalipoproteinemias [MeSH Descriptor]
Validated automatic mappings to BTNT
- Tangier disease [Disease (Nov.)]
disease_has_finding
- Rare Lesion [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients