33513003: Familial apolipoprotein C-II deficiency (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Evaluation finding\Measurement finding\...
• \Finding of substance level\Finding of lipid level\Lipids outside reference range\Lipid above reference range\Hyperlipidemia\...
• \Hyperlipidemia with lipid deposition in skin\Primary chylomicronemia\Chylomicronemia syndrome\Familial chylomicronemia syndrome\Familial apolipoprotein C-II deficiency
• \Endogenous hyperlipidemia\Primary genetic hyperlipidemia\Chylomicronemia syndrome\Familial chylomicronemia syndrome\Familial apolipoprotein C-II deficiency
• \Measurement finding outside reference range\Measurement finding above reference range\Lipid above reference range\Hyperlipidemia\Hyperlipidemia 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\Hyperlipidemia\Endogenous hyperlipidemia\Primary genetic hyperlipidemia\Chylomicronemia syndrome\Familial chylomicronemia syndrome\Familial apolipoprotein C-II deficiency
• \Measurement finding outside reference range\Lipids outside reference range\Lipid above reference range\Hyperlipidemia\Hyperlipidemia with lipid deposition in skin\Primary chylomicronemia\Chylomicronemia syndrome\Familial chylomicronemia syndrome\Familial apolipoprotein C-II deficiency
• \Measurement finding outside reference range\Lipids outside reference range\Lipid above reference range\Hyperlipidemia\Endogenous hyperlipidemia\Primary genetic hyperlipidemia\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\Hyperlipidemia\Hyperlipidemia 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\Hyperlipidemia\Endogenous hyperlipidemia\Primary genetic hyperlipidemia\Chylomicronemia syndrome\Familial chylomicronemia syndrome\Familial apolipoprotein C-II deficiency

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
55921014	Familial apolipoprotein C-II deficiency	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
55923012	Anapolipoproteinemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
485540016	Anapolipoproteinaemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
764927011	Familial apolipoprotein C-II deficiency (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module
4696705016	Familial apoC-II deficiency	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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