Homozygous Familial Hypercholesterolemia D000090542

Description

A rare inherited genetic disorder, one form of HYPERLIPOPROTEINEMIA TYPE II, characterized by high level of LOW-DENSITY LIPOPROTEIN (LDL) which if not treated could elevate the chance of heart attack at an early age.   MeSH

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Phase 4 Indicated Drugs (2)

Phase 1 Indicated Drugs (1)

Other Experimental Indicated Drugs (1)

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