Pancreatic triacylglycerol lipase deficiency

An autosomal recessive disorder caused by mutation(s) in the PNLIP gene, encoding pancreatic triacylglycerol lipase. The condition is characterized by absent or reduced pancreatic lipase.

Also known as: 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

0 clinical trials for this condition and its sub-types, 0 tagged with Pancreatic triacylglycerol lipase deficiency itself.