has material basis in germline mutation in APOA5 familial hyperlipidemia hyperlipoproteinemia type V https://rarediseases.info.nih.gov/diseases/6704/hyperlipoproteinemia-type-5 https://www.malacards.org/card/familial_apolipoprotein_a5_deficiency https://www.malacards.org/card/hyperlipoproteinemia_type_v_2 Orphanet:530849 A severe type of hyperlipidemia, sometimes familial, that is characterized by the elevation of both plasma chylomicrons and triglycerides contained in very-low-density lipoproteins. Type V hyperlipoproteinemia is often associated with diabetes mellitus and is not caused by reduced lipoprotein lipase activity as in hyperlipoproteinemia type I. MedDRA:10060755 MEDGEN:5693 hyperlipemia combined fat and carbohydrate-induced OMIM:144650 familial apolipoprotein A5 deficiency SCTID:34349009 UMLS:C0020481 hyperlipidemia type V Orphanet:70470 familial APOA5 deficiency major hyperlipidemia MESH:D006954 familial apolipoprotein A-V deficiency type V hyperlipoproteinemia hyperlipemia mixed hyperlipoproteinemia type 5 HLP type 5 MONDO:0007762 mixed hyperlipemia hyperchylomicronemia late onset DOID:0111421 GARD:0006704 DOID:1171