MeSH Browser

MeSH Supplementary: Hypercholesterolemia due to arg3500 mutation of Apo B-100
Unique ID: C536083
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536083
Entry Term(s): Hypercholesterolemia, familial, due to ligand-defective apolipoprotein B
Registry Number: 0
Heading Mapped to: *Hyperlipoproteinemia Type II
Frequency: 1
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Hypercholesterolemia due to arg3500 mutation of Apo B-100 MeSH Supplementary Concept Data 2024