33513003: Familial apolipoprotein C-II deficiency (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Evaluation finding\Measurement finding\...
• \Finding of substance level\Lipid level - finding\Lipids abnormal\Lipid above reference range\Hyperlipidaemia\...
• \Hyperlipidaemia with lipid deposition in skin\Primary chylomicronemia\Chylomicronemia syndrome\Familial chylomicronemia syndrome\Familial apolipoprotein C-II deficiency
• \Endogenous hyperlipidaemia\Primary genetic hyperlipidaemia\Chylomicronemia syndrome\Familial chylomicronemia syndrome\Familial apolipoprotein C-II deficiency
• \Measurement finding outside reference range\Measurement finding above reference range\Lipid above reference range\Hyperlipidaemia\Hyperlipidaemia with lipid deposition in skin\Primary chylomicronemia\Chylomicronemia syndrome\Familial chylomicronemia syndrome\Familial apolipoprotein C-II deficiency
• \Measurement finding outside reference range\Measurement finding above reference range\Lipid above reference range\Hyperlipidaemia\Endogenous hyperlipidaemia\Primary genetic hyperlipidaemia\Chylomicronemia syndrome\Familial chylomicronemia syndrome\Familial apolipoprotein C-II deficiency
• \Measurement finding outside reference range\Lipids abnormal\Lipid above reference range\Hyperlipidaemia\Hyperlipidaemia with lipid deposition in skin\Primary chylomicronemia\Chylomicronemia syndrome\Familial chylomicronemia syndrome\Familial apolipoprotein C-II deficiency
• \Measurement finding outside reference range\Lipids abnormal\Lipid above reference range\Hyperlipidaemia\Endogenous hyperlipidaemia\Primary genetic hyperlipidaemia\Chylomicronemia syndrome\Familial chylomicronemia syndrome\Familial apolipoprotein C-II deficiency
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Familial chylomicronemia syndrome\Familial apolipoprotein C-II deficiency
• \Disease\Familial disease\Familial chylomicronemia syndrome\Familial apolipoprotein C-II deficiency
• \Disease\Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Disorder of lipoprotein storage and metabolism\Hyperlipidaemia\Hyperlipidaemia with lipid deposition in skin\Primary chylomicronemia\Chylomicronemia syndrome\Familial chylomicronemia syndrome\Familial apolipoprotein C-II deficiency
• \Disease\Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Disorder of lipoprotein storage and metabolism\Hyperlipidaemia\Endogenous hyperlipidaemia\Primary genetic hyperlipidaemia\Chylomicronemia syndrome\Familial chylomicronemia syndrome\Familial apolipoprotein C-II deficiency

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4696705016	Familial apoC-II deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
485540016	Anapolipoproteinaemia	en	Synonym	Active	Case insensitive	SNOMED CT core
55921014	Familial apolipoprotein C-II deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
55922019	Apo-c-II deficiency	en	Synonym	Inactive	Case sensitive	SNOMED CT core
55923012	Anapolipoproteinemia	en	Synonym	Active	Case insensitive	SNOMED CT core
764927011	Familial apolipoprotein C-II deficiency (disorder)	en	Fully specified name	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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