Hypercholesterolemia, Autosomal Dominant, 3 MeSH Supplementary Concept Data 2025

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Concepts

MeSH Supplementary: Hypercholesterolemia, Autosomal Dominant, 3
Unique ID: C566337
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566337
Entry Term(s): FH3; HCHOLA3
Registry Numbers: 0
Heading Mapped to: *Hyperlipoproteinemias
Frequency: 1
Note: mutation in PCSK9
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Hypercholesterolemia, Autosomal Dominant, 3 Preferred

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