Disease: Hyperlipidemia, Familial Combined ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020474
Disease: Hyperlipidemia, Familial Combined
Hyperlipidemia, Familial Combined 		0.020 Biomarker disease LHGDN These results clearly demonstrate the genetically complex nature of FCHL and identify the PPARA gene as a modifier of the FCHL phenotype. 12468272 2002
CUI: C0020474
Disease: Hyperlipidemia, Familial Combined
Hyperlipidemia, Familial Combined 		0.020 Biomarker disease BEFREE These results clearly demonstrate the genetically complex nature of FCHL and identify the PPARA gene as a modifier of the FCHL phenotype. 12468272 2002
CUI: C0020474
Disease: Hyperlipidemia, Familial Combined
Hyperlipidemia, Familial Combined 		0.020 GeneticVariation disease BEFREE Molecular scanning of the human PPARa gene: association of the L162v mutation with hyperapobetalipoproteinemia. 10828087 2000