Also known as Fredrickson type I hyperlipoproteinemia (disorder), Fredrickson type I lipaemia, familial LPL deficiency, familial hyperchylomicronemia (disorder), familial hyperlipoproteinemia type I,
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familial hyperlipemia characterized by a deficiency of the enzyme lipoprotein lipase and the subsequent build up of chylomicrons and increased plasma concentration of triglycerides
Discovered by embedding cosine similarity (sentence-transformers MiniLM, 384-dim).