inborn errors lipid metabolism hyperlipoproteinemia familial combined hyperlipidemia Familial combined hyperlipidaemia familial combined hyperlipidemia (disorder) [Ambiguous] GeneRIF:12006395 GeneRIF:15959806 Familial multiple lipoprotein-type hyperlipidemia (disorder) familial combined hyperlipidemia Type IIb Hyperlipoproteinemia Hyperapobetalipoproteinemia Familial hyperlipoproteinaemia type IIb GeneRIF:15976322 Multiple Lipoprotein-Type Hyperlipidemias Mixed hyperlipidaemia SNOMEDCT:238040008 GeneRIF:11979403 Fredrickson type IIb hyperlipoproteinemia GeneRIF:12468272 URI: http://www.ebi.ac.uk/cellline#familial_combined_hyperlipidemia Multiple-type hyperlipidaemia Multiple-type hyperlipidemia MSH:D006950 Mixed hyperlipidemia ICD9:272.2 GeneRIF:15136067 DOID:13809 GeneRIF:12738753 Combined Hyperlipidemias, Familial GeneRIF:14680975 GeneRIF:16076849 Lipoprotein-Type Hyperlipidemia, Multiple James Malone Familial hyperlipoproteinemia type IIb hyperbetalipoproteinemia with prebetalipoproteinemia SNOMEDCT:267434003 FCHL - Familial combined hyperlipidemia FCHL - Familial combined hyperlipidaemia SNOMEDCT:299465007 Fredrickson type IIb hyperlipoproteinaemia Familial multiple lipoprotein-type hyperlipidemia Familial multiple lipoprotein-type hyperlipidaemia A type of familial lipid metabolism disorder characterized by a variable pattern of elevated plasma CHOLESTEROL and/or TRIGLYCERIDES. Multiple genes on different chromosomes may be involved, such as the major late transcription factor (UPSTREAM STIMULATORY FACTORS) on CHROMOSOME 1. GeneRIF:12401883 mixed hyperlipidemia (disorder) GeneRIF:12370850 Hyperapobetalipoproteinaemia GeneRIF:14991056 familial combined hyperlipidemia (disorder)