has material basis in germline mutation in LMF1 autosomal recessive disease lipase deficiency, combined https://github.com/monarch-initiative/mondo/issues/8644 https://rarediseases.info.nih.gov/diseases/10244/lipase-deficiency-combined https://www.malacards.org/card/lipase_deficiency_combined_2 A rare disorder caused by mutation in the LMF1 gene resulting in combined lipase deficiency with concomitant hypertriglyceridemia and associated disorders. UMLS:C1855498 MESH:C535904 lipase deficiency, combined NCIT:C126558 OMIM:246650 lipoprotein lipase deficiency with hepatic triglyceride lipase deficiency MEDGEN:340886 DOID:0111422 combined lipase deficiency familial lipase maturation factor 1 deficiency GARD:0010244 MONDO:0009527 lipase deficiency combined Orphanet:535453 LPL and HL deficiency LPL and HTGL deficiency familial chylomicronemia syndrome