Familial lipoprotein lipase deficiency
Also known as Fredrickson type I hyperlipoproteinemia, Fredrickson type I lipaemia, LPL deficiency, familial LPL deficiency+25 more
Fredrickson type I hyperlipoproteinemia, Fredrickson type I lipaemia, LPL deficiency, familial LPL deficiency, familial hyperlipoproteinemia type I, familial lipoprotein lipase deficiency (disorder) [ambiguous], familial lipoprotein lipase deficiency with type I phenotype, high density lipoprotein cholesterol level QTL 11, hypercholesterinaemic xanthomatosis, hyperchylomicronemia, mixed hyperglyceridemia, Burger-Grutz syndrome, chylomicronemia, familial, endogenous hypertriglyceridaemia, familial fat-induced hypertriglyceridemia, familial hyperchylomicronemia, hyperchylomicronemia, familial, hyperlipemia, essential familial, hyperlipemia, idiopathic, Burger-Grutz type, hyperlipoproteinemia, type 1A, lipase D deficiency, lipd deficiency, lipoprotein lipase deficiency, lipoprotein lipase deficiency, familial, familial chylomicronemia syndrome, hyperlipoproteinemia type I, hyperlipoproteinemia, type 1, hyperlipoproteinemia, type I, type I hyperlipoproteinemia.
What's happening now
An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.
Clinical trials
The current development programme across all trial phases.
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.
Fredrickson type I hyperlipoproteinemia, Fredrickson type I lipaemia, LPL deficiency, familial LPL deficiency, familial hyperlipoproteinemia type I, familial lipoprotein lipase deficiency (disorder) [ambiguous], familial lipoprotein lipase deficiency with type I phenotype, high density lipoprotein cholesterol level QTL 11, hypercholesterinaemic xanthomatosis, hyperchylomicronemia, mixed hyperglyceridemia, Burger-Grutz syndrome, chylomicronemia, familial, endogenous hypertriglyceridaemia, familial fat-induced hypertriglyceridemia, familial hyperchylomicronemia, hyperchylomicronemia, familial, hyperlipemia, essential familial, hyperlipemia, idiopathic, Burger-Grutz type, hyperlipoproteinemia, type 1A, lipase D deficiency, lipd deficiency, lipoprotein lipase deficiency, lipoprotein lipase deficiency, familial, familial chylomicronemia syndrome, hyperlipoproteinemia type I, hyperlipoproteinemia, type 1, hyperlipoproteinemia, type I, type I hyperlipoproteinemia
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Clinical trials — ClinicalTrials.gov (U.S. National Library of Medicine)
- Related entities are derived from literature co-mention (studied together) — associative, not causal.