OMOP Concept 4170226
Disorder of lipoprotein AND/OR lipid metabolism
StandardConditionSNOMED48286001Disorder
Maps from
2
Descendants
279
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
2 source codes normalize to Disorder of lipoprotein AND/OR lipid metabolism via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 142054 | Disorder of lipoprotein and/or lipid metabolism | Non-standard |
| Nebraska Lexicon | 48286001 | Disorder of lipid and lipoprotein metabolism | Non-standard |
Synonyms
Alternative names recorded for Disorder of lipoprotein AND/OR lipid metabolism across source vocabularies.
- Disorder of lipid and lipoprotein metabolism
- Disorder of lipoprotein AND/OR lipid metabolism (disorder)
- trastorno del metabolismo de lipoproteínas y lípidos
- trastorno del metabolismo de lipoproteínas Y/O lípidos
- trastorno del metabolismo de lipoproteínas Y/O lípidos (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(3)Roll up to these when you need a wider cohort.
Narrower concepts
(279)Included automatically when you query with descendants.
- 1Disorder of fatty acid metabolism
- 1Disorder of lipid metabolism
- 1Disorder of lipid storage and metabolism
- 1Disorder of lipoprotein storage and metabolism
- 1Dyslipidemia
- 1Fat overload syndrome
- 1Hypolipoproteinemia
- 1Inborn error of lipoprotein metabolism
- 1Lipofuscinosis
- 1Lipoprotein deficiency disorder
- 1Xanthoma due to abnormality of lipid metabolism
- 23-hydroxy-3-methylglutaryl-coenzyme A synthase deficiency
- 2Abetalipoproteinemia
- 2Abnormal lipid deposits
- 2Apolipoprotein A-I deficiency
- 2Apolipoprotein A-I variant disorder
- 2Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction
- 2Carnitine deficiency due to inborn error of metabolism
- 2Carnitine palmitoyltransferase deficiency
- 2CHILD syndrome
- 2CK syndrome
- 2Combined deficiency of long chain 3-hydroxyacyl-CoA dehydrogenase and enoyl-CoA hydratase
- 2Combined malonic and methylmalonic aciduria
- 2Combined pancreatic lipase and colipase deficiency
- 2Complex dyslipidemia
- 2Congenital ichthyosis, intellectual disability, spastic quadriplegia syndrome
- 2Deficiency of 2,4-dienoyl-CoA reductase
- 2Deficiency of carnitine acetyltransferase
- 2Disorder of cholesterol catabolism
- 2Disorder of cholesterol metabolism
- 2Disorder of cholesterol synthesis
- 2Dyslipidemia due to type 1 diabetes mellitus
- 2Dyslipidemia due to type 2 diabetes mellitus
- 2Familial disease with storage of sterols (other than cholesterol)
- 2Familial hyperlipoproteinemia
- 2Familial hypoalphalipoproteinemia
- 2Familial hypobetalipoproteinemia
- 2Familial hypolipoproteinemia
- 2Familial lipoprotein deficiency
- 2Familial steroid-resistant nephrotic syndrome with adrenal insufficiency
- 2Farber's lipogranulomatosis
- 2Fatty acid oxidation defect
- 2Gangliosidosis
- 2Glutaric aciduria, type 2
- 2GM3 synthase deficiency
- 2Hepatic lipase deficiency
- 2High density lipoprotein deficiency
- 2HSMN IV
- 2Hyperimmunoglobulinemia D with periodic fever
- 2Hyperlipidemia
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