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Familial combined hyperlipidemia

Disease ID:348
Name:Familial combined hyperlipidemia
Associated with:1 target
Database Links
Disease Ontology: DOID:13809


C5a2 receptor
Mutations:  C5a2 receptor is associated with 1 mutation. Click here for details


No ligand related data available for Familial combined hyperlipidemia


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1. Marcil M, Vu H, Cui W, Dastani Z, Engert JC, Gaudet D, Castro-Cabezas M, Sniderman AD, Genest J, Cianflone K. (2006) Identification of a novel C5L2 variant (S323I) in a French Canadian family with familial combined hyperlipemia. Arterioscler Thromb Vasc Biol, 26 (7): 1619-25. [PMID:16627811]

2. Zheng YY, Xie X, Ma YT, Yang YN, Fu ZY, Li XM, Liu F, Yang SJ, Ma X, Chen BD. (2011) S323I polymorphism of the C5L2 gene was not identified in a Chinese population with familial combined hyperlipidemia or with type 2 diabetes. Genet Mol Res, 10 (4): 3256-66. [PMID:22194190]