OMOP Concept 4170226
Disorder of lipoprotein AND/OR lipid metabolism
StandardConditionSNOMED48286001Disorder
Maps from
7
Descendants
291
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
7 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 |
| CIM10 | E78 | Disorders of lipoprotein metabolism and other lipidaemias | Non-standard |
| ICD10 | E78 | Disorders of lipoprotein metabolism and other lipidaemias | Non-standard |
| ICD10CM | E78 | Disorders of lipoprotein metabolism and other lipidemias | Non-standard |
| ICD10CN | E78 | Disorders of lipoprotein metabolism and other lipidaemias | Non-standard |
| ICD10GM | E78 | Disorders of lipoprotein metabolism and other lipidaemias | Non-standard |
| KCD7 | E78 | Disorders of lipoprotein metabolism and other lipidaemias | 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
(291)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 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
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