OMOP Concept 4079889
Familial hypobetalipoproteinemia - homozygous form
StandardConditionSNOMED238093009Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
Concept Lookup Tool
Search 11M+ concepts across SNOMED, RxNorm, ICD-10 & LOINC.
Source codes that map to this concept
1 source code normalizes to Familial hypobetalipoproteinemia - homozygous form via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 238093009 | Familial hypobetalipoproteinaemia - homozygous form | Non-standard |
Synonyms
Alternative names recorded for Familial hypobetalipoproteinemia - homozygous form across source vocabularies.
- Familial hypobetalipoproteinaemia - homozygous form
- Familial hypobetalipoproteinemia - homozygous form (disorder)
- hipobetalipoproteinemia familiar - forma homocigota
- hipobetalipoproteinemia familiar - forma homocigota (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
Get this concept via the API
Resolve Familial hypobetalipoproteinemia - homozygous form - and every code that maps to it - over HTTPS, against the current vocabulary release. No downloads, no local database.
curl "https://api.omophub.com/v1/concepts/4079889?include_relationships=true" \
-H "Authorization: Bearer $OMOPHUB_API_KEY"Get your free API key3,000 calls/month free · no credit card