33513003: Familial apolipoprotein C-II deficiency (disorder)

• SNOMED CT Concept\constatation clinique\...
• \Evaluation finding\Measurement finding\...
• \Finding of substance level (finding)\Lipid level - finding\Lipids abnormal\Increased lipid\hyperlipidémie\...
• \Hyperlipidemia with lipid deposition in skin (disorder)\Primary chylomicronemia (disorder)\Chylomicronemia syndrome (disorder)\Familial chylomicronemia syndrome (disorder)\déficit familial en apolipoprotéine C-II (trouble)
• \Endogenous hyperlipidaemia\Primary genetic hyperlipidemia (disorder)\Chylomicronemia syndrome (disorder)\Familial chylomicronemia syndrome (disorder)\déficit familial en apolipoprotéine C-II (trouble)
• \Measurement finding outside reference range\Measurement finding above reference range\Increased lipid\hyperlipidémie\Hyperlipidemia with lipid deposition in skin (disorder)\Primary chylomicronemia (disorder)\Chylomicronemia syndrome (disorder)\Familial chylomicronemia syndrome (disorder)\déficit familial en apolipoprotéine C-II (trouble)
• \Measurement finding outside reference range\Measurement finding above reference range\Increased lipid\hyperlipidémie\Endogenous hyperlipidaemia\Primary genetic hyperlipidemia (disorder)\Chylomicronemia syndrome (disorder)\Familial chylomicronemia syndrome (disorder)\déficit familial en apolipoprotéine C-II (trouble)
• \Measurement finding outside reference range\Lipids abnormal\Increased lipid\hyperlipidémie\Hyperlipidemia with lipid deposition in skin (disorder)\Primary chylomicronemia (disorder)\Chylomicronemia syndrome (disorder)\Familial chylomicronemia syndrome (disorder)\déficit familial en apolipoprotéine C-II (trouble)
• \Measurement finding outside reference range\Lipids abnormal\Increased lipid\hyperlipidémie\Endogenous hyperlipidaemia\Primary genetic hyperlipidemia (disorder)\Chylomicronemia syndrome (disorder)\Familial chylomicronemia syndrome (disorder)\déficit familial en apolipoprotéine C-II (trouble)
• \Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Familial chylomicronemia syndrome (disorder)\déficit familial en apolipoprotéine C-II (trouble)
• \Disease\Familial disease\Familial chylomicronemia syndrome (disorder)\déficit familial en apolipoprotéine C-II (trouble)
• \Disease\trouble métabolique\troubles du métabolisme des lipoprotéines et/ou des lipides\troubles du stockage et du métabolisme des lipoprotéines\hyperlipidémie\Hyperlipidemia with lipid deposition in skin (disorder)\Primary chylomicronemia (disorder)\Chylomicronemia syndrome (disorder)\Familial chylomicronemia syndrome (disorder)\déficit familial en apolipoprotéine C-II (trouble)
• \Disease\trouble métabolique\troubles du métabolisme des lipoprotéines et/ou des lipides\troubles du stockage et du métabolisme des lipoprotéines\hyperlipidémie\Endogenous hyperlipidaemia\Primary genetic hyperlipidemia (disorder)\Chylomicronemia syndrome (disorder)\Familial chylomicronemia syndrome (disorder)\déficit familial en apolipoprotéine C-II (trouble)

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
418661000241117	déficit familial en apolipoprotéine C-II (trouble)	fr	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
4696705016	Familial apoC-II deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
485540016	Anapolipoproteinaemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
55921014	Familial apolipoprotein C-II deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
55923012	Anapolipoproteinemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
764927011	Familial apolipoprotein C-II deficiency (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
973331000172112	déficit familial en apolipoprotéine C-II	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
995831000172113	déficit familial en apoC-II	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)

Expanded Value Set

This concept is not in any reference sets

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