C126558Level 6
Combined Lipase Deficiency
**Semantic type:** Disease or Syndrome
**Definition:** A rare disorder caused by mutation in the LMF1 gene resulting in combined lipase deficiency with concomitant hypertriglyceridemia and associated disorders.
GET
/api/v1/systems/nci_thesaurus/nodes/C126558Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.