Lipase deficiency, combined

A rare disorder caused by mutation in the LMF1 gene resulting in combined lipase deficiency with concomitant hypertriglyceridemia and associated disorders.

Also known as: combined lipase deficiency, familial lipase maturation factor 1 deficiency, lipase deficiency, combined, LPL and HL deficiency, LPL and HTGL deficiency, lipase deficiency combined, lipoprotein lipase deficiency with hepatic triglyceride lipase deficiency

0 clinical trials for this condition and its sub-types, 0 tagged with Lipase deficiency, combined itself.