OMOP Concept 4295609

Familial hypercholesterolemia due to genetic defect of apolipoprotein B

StandardConditionSNOMED403831006Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2003
Valid to
31 Dec 2099
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Source codes that map to this concept

1 source code normalizes to Familial hypercholesterolemia due to genetic defect of apolipoprotein B via the OMOP "Maps to" relationship.

Synonyms

Alternative names recorded for Familial hypercholesterolemia due to genetic defect of apolipoprotein B across source vocabularies.

  • Familial hypercholesterolaemia due to genetic defect of apolipoprotein B
  • Familial hypercholesterolemia due to genetic defect of apolipoprotein B (disorder)
  • hipercolesterolemia familiar por defecto genético de apolipoproteína B
  • hipercolesterolemia familiar por defecto genético de apolipoproteína B (trastorno)
  • Hypercholesterolaemia due to apolipoprotein B gene defect
  • Hypercholesterolemia due to apolipoprotein B gene defect

Where it sits in the hierarchy

Ordered by distance - 1 is a direct parent or child.

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