FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term hyperlipoproteinemia type III ID (Ontology) DOID:3145 (Human Disease)
Definition A familial hyperlipidemia that has_material_basis_in by homozygous, compound heterozygous, or heterozygous mutation in the APOE gene on chromosome 19q13.
Also Known As "carbohydrate induced hyperlipemia" ; "familial hypercholesterolaemia with hyperlipaemia" ; "familial type 3 hyperlipoproteinemia" (for all, see Synonyms field below)
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Spanning Tree (Parents/Children)
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  lipid metabolism disorder
   |__familial hyperlipidemia
       |__hyperlipoproteinemia type III
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Is a familial hyperlipidemia
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Synonyms
  • "carbohydrate induced hyperlipemia" EXACT
    "familial hypercholesterolaemia with hyperlipaemia" EXACT
    "familial type 3 hyperlipoproteinemia" EXACT
    "Remnant hyperlipidemia" EXACT
Secondary IDs
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MESH:D006952
MIM:617347
NCI:C34710
SNOMEDCT_US_2023_03_01:42569002
UMLS_CUI:C0020479