Hypercholesterolemia, autosomal dominant, 3
Also known as PCSK9 familial hypercholesterolemia, familial hypercholesterolemia caused by mutation in PCSK9, hypercholesterolemia, autosomal dominant, type 3, hypercholesterolemia, familial, 3+4 more
PCSK9 familial hypercholesterolemia, familial hypercholesterolemia caused by mutation in PCSK9, hypercholesterolemia, autosomal dominant, type 3, hypercholesterolemia, familial, 3, low density lipoprotein cholesterol level QTL 1, Fh3, HCHOLA3, low density lipoprotein cholesterol level quantitative trait locus 1.
What's happening now
An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.
Associated genes
Genes associated with this disease in the canonical knowledge graph (Open Targets evidence). Number shows the association score.
Disease biology
Proteins whose encoding gene is associated with this disease, reached through the canonical gene→disease graph. Number shows the gene's association score.
Reference
Authoritative identity, definition & identifiers.
PCSK9 familial hypercholesterolemia, familial hypercholesterolemia caused by mutation in PCSK9, hypercholesterolemia, autosomal dominant, type 3, hypercholesterolemia, familial, 3, low density lipoprotein cholesterol level QTL 1, Fh3, HCHOLA3, low density lipoprotein cholesterol level quantitative trait locus 1
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Related entities are derived from literature co-mention (studied together) — associative, not causal.