720940008: Hepatic lipase deficiency (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Hepatic lipase deficiency
• \Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Dyslipidaemia\Hepatic lipase deficiency

Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3322576010	Hepatic lipase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
3322577018	Hyperlipidaemia due to hepatic triglyceride lipase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
3322579015	Hepatic lipase deficiency (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3322580017	Hyperlipidemia due to hepatic triglyceride lipase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
3322578011	A disorder that affects the ability to break down lipids leading to increased amounts of triglycerides and cholesterol in the blood. Caused by mutations in the lipase C hepatic type (LIPC) gene. This gene provides instructions for making hepatic lipase. LIPC gene mutations prevent the release of hepatic lipase from the liver or decrease the enzyme's activity in the bloodstream. As a result very low-density lipoproteins and intermediate-density lipoproteins are not efficiently converted into LDLs, and HDLs carrying cholesterol and triglyceride remain in the bloodstream. It is unclear what effect this change in lipid levels has on people with hepatic lipase deficiency.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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