Preferred Label : Familial defective apolipoprotein B-100;
ICD-11 definition : This is an autosomal dominant disorder resulting from a missense mutation which reduces
the affinity of apoB-100 for the low-density lipoprotein receptor (LDL Receptor).;
Origin ID : 2106114192;
Automatic exact mappings (from CISMeF team)
This is an autosomal dominant disorder resulting from a missense mutation which reduces
the affinity of apoB-100 for the low-density lipoprotein receptor (LDL Receptor).
