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Familial combined hyperlipidemia

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

Targets

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

Ligands

No ligand related data available for Familial combined hyperlipidemia

References

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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]