403828005: Familial lipoprotein lipase deficiency with type V phenotype (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Evaluation finding\Measurement finding\...
• \Finding of substance level\Lipid level - finding\Lipids abnormal\Lipid above reference range\Hyperlipidaemia\Hypertriglyceridaemia\Primary hypertriglyceridaemia\Familial hypertriglyceridaemia\Familial hyperchylomicronaemia\Familial lipoprotein lipase deficiency with type V phenotype
• \Measurement finding outside reference range\Measurement finding above reference range\Lipid above reference range\Hyperlipidaemia\Hypertriglyceridaemia\Primary hypertriglyceridaemia\Familial hypertriglyceridaemia\Familial hyperchylomicronaemia\Familial lipoprotein lipase deficiency with type V phenotype
• \Measurement finding outside reference range\Lipids abnormal\Lipid above reference range\Hyperlipidaemia\Hypertriglyceridaemia\Primary hypertriglyceridaemia\Familial hypertriglyceridaemia\Familial hyperchylomicronaemia\Familial lipoprotein lipase deficiency with type V phenotype
• \Disease\Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Disorder of lipoprotein storage and metabolism\Hyperlipidaemia\Hypertriglyceridaemia\Primary hypertriglyceridaemia\Familial hypertriglyceridaemia\Familial hyperchylomicronaemia\Familial lipoprotein lipase deficiency with type V phenotype

Status: current, Primitive. Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
1771754012	Familial lipoprotein lipase deficiency with type V phenotype (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
1782835012	Familial lipoprotein lipase deficiency with type V phenotype	en	Synonym	Active	Initial character case insensitive	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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