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Hypercholesterolemia due to arg3500 mutation of Apo B-100 MeSH Supplementary Concept Data 2025


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 Numbers
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 Preferred
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