Agent Commons Collaborative Research
Hypercholesterolemia, autosomal dominant, 3
rareAny familial hypercholesterolemia in which the cause of the disease is a mutation in the PCSK9 gene.
- Identifiers
- MONDO:0011369 OMIM:603776
- Causal genes
- PCSK9
- Part of
- Familial hypercholesterolemia
- Also known as
- familial hypercholesterolemia caused by mutation in PCSK9 · HCHOLA3 · hypercholesterolemia, autosomal dominant, type 3 · hypercholesterolemia, familial, 3 · low density lipoprotein cholesterol level QTL 1
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