OMOP Concept 4029265
Lecithin cholesterol acyltransferase deficiency
StandardConditionSNOMED238091006Disorder
Maps from
1
Descendants
2
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
1 source code normalizes to Lecithin cholesterol acyltransferase deficiency via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 130245 | Phosphatidylcholine-sterol acyltransferase deficiency | Non-standard |
Synonyms
Alternative names recorded for Lecithin cholesterol acyltransferase deficiency across source vocabularies.
- deficiencia de lecitina colesterol aciltransferasa
- deficiencia de lecitina colesterol aciltransferasa (trastorno)
- LCAT deficiency
- LCAT (lecithin-cholesterol acyltransferase) deficiency
- Lecithin cholesterol acyltransferase deficiency (disorder)
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.
- 1Cholesterol level - finding
- 1Corneal opacity
- 1Genetic disease
- 1High density lipoprotein below reference range
- 1Hypoalphalipoproteinemia
- 2Corneal degeneration
- 2Disease
- 2Lesion of cornea
- 2Lipid level - finding
- 2Lipoprotein below reference range
- 2Lipoprotein deficiency disorder
- 3Clinical finding
- 3Degenerative disorder of eye
- 3Disorder of cornea
- 3Disorder of lipoprotein AND/OR lipid metabolism
- 3Finding of substance level
- 3Lesion of eye
- 3Lipid below reference range
- 3Protein level - finding
- 4Anomaly of eye
- 4Corneal finding
- 4Degenerative disorder
- 4Disorder of anterior segment of eye
- 4Lipids outside reference range
- 4Measurement finding
Showing 25 of 41. Retrieve the full set via the API.
Narrower concepts
(2)Included automatically when you query with descendants.
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