OMOP Concept 4036109
Familial hypoalphalipoproteinemia
StandardConditionSNOMED15346004Disorder
Maps from
4
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
4 source codes normalize to Familial hypoalphalipoproteinemia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 140572 | Familial hypoalphalipoproteinemia | Non-standard |
| MeSH | C538394 | Hdl Deficiency, Type 2 | Non-standard |
| Nebraska Lexicon | 15346004 | Familial high density lipoprotein deficiency | Non-standard |
| Read | C325.11 | Tangier disease | Non-standard |
Synonyms
Alternative names recorded for Familial hypoalphalipoproteinemia across source vocabularies.
- A - alphalipoproteinaemia neuropathy
- A - alphalipoproteinemia neuropathy
- Alphalipoproteinaemia neuropathy
- Alphalipoproteinemia neuropathy
- analfalipoproteinemia
- Analphalipoproteinaemia
- Analphalipoproteinemia
- Analphaliproteinaemia
- Analphaliproteinemia
- Cholesterol thesaurismosis
- deficiencia familiar de HDL
- deficiencia familiar de lipoproteína de alta densidad
- Familial HDL deficiency
- Familial high density lipoprotein deficiency
- Familial hypoalphalipoproteinaemia
- Familial hypoalphalipoproteinemia (disorder)
- hipoalfalipoproteinemia familiar
- hipoalfalipoproteinemia familiar (trastorno)
- neuropatía por alfalipoproteinemia
- tesaurismosis por colesterol
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(13)Roll up to these when you need a wider cohort.
- 1Familial lipoprotein deficiency
- 1Lipoprotein deficiency disorder
- 2Disorder of lipoprotein AND/OR lipid metabolism
- 2Inborn error of lipoprotein metabolism
- 3Inborn error of metabolism
- 3Metabolic disease
- 4Congenital disease
- 4Disease
- 4Hereditary metabolic disease
- 5Clinical finding
- 5Disorder of fetus and/or newborn
- 5Hereditary disease
- 6Genetic disease
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