Hypercholesterolemia, familial, 4

An autosomal recessive condition caused by mutation(s) in the LDLRAP1 gene, encoding low density lipoprotein receptor adaptor protein 1. The phenotype is similar to that of familial hypercholesterolemia, but generally considered to be a milder form of hypercholesterolemia.

Also known as: ARH, ARH1, ARH2, autosomal recessive hypercholesterolemia 1, autosomal recessive hypercholesterolemia 2, FHCB1, FHCB1, formerly, FHCB2

0 clinical trials for this condition and its sub-types, 0 tagged with Hypercholesterolemia, familial, 4 itself.