OMOP Concept 4029893
Familial hypobetalipoproteinemia - heterozygous form
StandardConditionSNOMED238094003Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Familial hypobetalipoproteinemia - heterozygous form via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 238094003 | Familial hypobetalipoproteinaemia - heterozygous form | Non-standard |
Synonyms
Alternative names recorded for Familial hypobetalipoproteinemia - heterozygous form across source vocabularies.
- Familial hypobetalipoproteinaemia - heterozygous form
- Familial hypobetalipoproteinemia - heterozygous form (disorder)
- hipobetalipoproteinemia familiar - forma heterocigota
- hipobetalipoproteinemia familiar - forma heterocigota (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(14)Roll up to these when you need a wider cohort.
- 1Familial hypobetalipoproteinemia
- 2Familial lipoprotein deficiency
- 2Lipoprotein deficiency disorder
- 3Disorder of lipoprotein AND/OR lipid metabolism
- 3Inborn error of lipoprotein metabolism
- 4Inborn error of metabolism
- 4Metabolic disease
- 5Congenital disease
- 5Disease
- 5Hereditary metabolic disease
- 6Clinical finding
- 6Disorder of fetus and/or newborn
- 6Hereditary disease
- 7Genetic disease
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