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Disease

Pancreatic triacylglycerol lipase deficiency

Also known as pancreatic triglyceride lipase deficiency, PL deficiency, PNLIPD, colipase, congenital absence of pancreatic+5 more

pancreatic triglyceride lipase deficiency, PL deficiency, PNLIPD, colipase, congenital absence of pancreatic, lipase and colipase, congenital absence of pancreatic, lipase and colipase, deficiency of, lipase, congenital absence of pancreatic, pancreatic colipase deficiency, pancreatic lipase deficiency.

3
Associated genes
1
Related proteins

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Associated genes

3 matches

Genes associated with this disease in the canonical knowledge graph (Open Targets evidence). Number shows the association score.

Disease biology

1 match

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.

Synonyms

pancreatic triglyceride lipase deficiency, PL deficiency, PNLIPD, colipase, congenital absence of pancreatic, lipase and colipase, congenital absence of pancreatic, lipase and colipase, deficiency of, lipase, congenital absence of pancreatic, pancreatic colipase deficiency, pancreatic lipase deficiency

References & data sources
  • Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
  • Related entities are derived from literature co-mention (studied together) — associative, not causal.