OMOP Concept 45765429
Chylomicron retention disease
StandardConditionSNOMED702364003Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2014
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Chylomicron retention disease via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C535460 | Chylomicron retention disease | Non-standard |
Synonyms
Alternative names recorded for Chylomicron retention disease across source vocabularies.
- Anderson syndrome
- Chylomicron retention disease (disorder)
- enfermedad por retención de quilomicrones
- enfermedad por retención de quilomicrones (trastorno)
- Lipid transport defect of intestine
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(41)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Digestive system hereditary disorder
- 1Disorder of digestive system specific to fetus OR newborn
- 1Familial hypobetalipoproteinemia
- 1Intestinal malabsorption of fat
- 2Autosomal hereditary disorder
- 2Disorder of digestive system
- 2Familial lipoprotein deficiency
- 2Fetal and/or neonatal disorder
- 2Hereditary disorder by system
- 2Intestinal malabsorption
- 2Lipoprotein deficiency disorder
- 3Digestive system finding
- 3Disease
- 3Disorder of body system
- 3Disorder of lipoprotein AND/OR lipid metabolism
- 3Disorder of small intestine
- 3Hereditary disease
- 3Inborn error of lipoprotein metabolism
- 3Malabsorption syndrome
- 4Clinical finding
- 4Disorder of gastrointestinal tract
- 4Disorder of intestine
- 4Finding of small intestine
- 4Genetic disease
Showing 25 of 41. Retrieve the full set via the API.
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