OMOP Concept 37162785
Familial chylomicronemia syndrome
StandardConditionSNOMED1197489003Disorder
Maps from
0
Descendants
2
Valid from
28 Feb 2022
Valid to
31 Dec 2099
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Synonyms
Alternative names recorded for Familial chylomicronemia syndrome across source vocabularies.
- Familial chylomicronemia syndrome (disorder)
- síndrome de quilomicronemia familiar
- síndrome de quilomicronemia familiar (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(25)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Chylomicronemia syndrome
- 1Familial disease
- 2Autosomal hereditary disorder
- 2Disease
- 2Primary chylomicronemia
- 2Primary genetic hyperlipidemia
- 3Clinical finding
- 3Endogenous hyperlipidemia
- 3Hereditary disease
- 3Hyperlipidemia with lipid deposition in skin
- 4Genetic disease
- 4Hyperlipidemia
- 5Disorder of lipoprotein storage and metabolism
- 5Lipid above reference range
- 6Disorder of lipoprotein AND/OR lipid metabolism
- 6Lipids outside reference range
- 6Measurement finding above reference range
- 7Lipid level - finding
- 7Measurement finding outside reference range
- 7Metabolic disease
- 8Finding of substance level
- 8Measurement finding
- 9Evaluation finding
- 10Procedure related finding
Narrower concepts
(2)Included automatically when you query with descendants.
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