A familial hyperlipidemia that has_material_basis_in by homozygous, compound heterozygous, or heterozygous mutation in the APOE gene on chromosome 19q13.
synonyms:
OMIM:617347,
SNOMEDCT_US_2023_03_01:42569002,
UMLS_CUI:C0020479,
MESH:D006952,
familial type 3 hyperlipoproteinemia,
Remnant hyperlipidemia,
familial hypercholesterolaemia with hyperlipaemia,
