Other hyperlipidemia

Preferred Label : Other hyperlipidemia;

Inclusion CIM-10 : Familial combined hyperlipidemia;

Diag associé à un acte (%) : 92.0;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

E784;

UMLS CUI

C0348494;

Automatic exact mappings (from CISMeF team)
- Familial combined hyperlipidemia (disorder) [SNOMED CT concept]
- Hyperlipidemia, familial combined, 3 [OMIM Phenotype]
- Hyperlipoproteinemia, Type IIb [NCIt concept]
- cholesterol [MedlinePlus Topic]
- cholesterol levels: what you need to know [MedlinePlus Topic]
- familial combined hyperlipidemia [DO Concept]
- hyperlipidemia, familial combined [MeSH Descriptor]
- hyperlipidemia, familial combined [MeSH concept]
- triglycerides [MedlinePlus Topic]
Orphanet concepts
- Cholesterol-ester transfer protein deficiency [ORDO Disease]
- Hyperalphalipoproteinemia [ORDO Disease]
- Hyperlipidemia due to hepatic triacylglycerol lipase deficiency [ORDO Disease]
- Laminopathy type Decaudain-Vigouroux [ORDO Disease]
- Rare dyslipidemia [ORDO Disease]
- Rare hyperlipidemia [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Other and unspecified hyperlipidemia [ICD-9 code]

Keyword's position in hierarchy(ies) :

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