OMOP Concept 37167480
Familial lecithin cholesterol acyltransferase deficiency
StandardConditionSNOMED1264565005Disorder
Maps from
1
Descendants
0
Valid from
28 Feb 2023
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Familial lecithin cholesterol acyltransferase deficiency via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | D007863 | Lecithin Cholesterol Acyltransferase Deficiency | Non-standard |
Synonyms
Alternative names recorded for Familial lecithin cholesterol acyltransferase deficiency across source vocabularies.
- Complete LCAT deficiency
- Complete LCAT (lecithin-cholesterol acyltransferase) deficiency
- deficiencia completa de LCAT
- deficiencia familiar de LCAT
- deficiencia familiar de lecitina-colesterol-acil-transferasa
- deficiencia familiar de lecitina-colesterol-acil-transferasa (trastorno)
- Familial lecithin cholesterol acyltransferase deficiency (disorder)
- Norum disease
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(43)Roll up to these when you need a wider cohort.
- 1Familial disease
- 1Lecithin cholesterol acyltransferase deficiency
- 2Cholesterol level - finding
- 2Corneal opacity
- 2Disease
- 2Genetic disease
- 2High density lipoprotein below reference range
- 2Hypoalphalipoproteinemia
- 3Clinical finding
- 3Corneal degeneration
- 3Lesion of cornea
- 3Lipid level - finding
- 3Lipoprotein below reference range
- 3Lipoprotein deficiency disorder
- 4Degenerative disorder of eye
- 4Disorder of cornea
- 4Disorder of lipoprotein AND/OR lipid metabolism
- 4Finding of substance level
- 4Lesion of eye
- 4Lipid below reference range
- 4Protein level - finding
- 5Anomaly of eye
- 5Corneal finding
- 5Degenerative disorder
- 5Disorder of anterior segment of eye
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