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

SNOMED CT Concept\Clinical finding (finding)\...

\Procedure related finding\Evaluation finding\Measurement finding\...

\Finding of substance level (finding)\Lipid level - finding\Lipids outside reference range\Lipid above reference range\Hyperlipidemia (disorder)\Hypertriglyceridaemia\Primary hypertriglyceridaemia\Familial hypertriglyceridemia\Familial hyperchylomicronemia (disorder)\Familial lipoprotein lipase deficiency with type V phenotype (disorder)

\Measurement finding outside reference range\Measurement finding above reference range (finding)\Lipid above reference range\Hyperlipidemia (disorder)\Hypertriglyceridaemia\Primary hypertriglyceridaemia\Familial hypertriglyceridemia\Familial hyperchylomicronemia (disorder)\Familial lipoprotein lipase deficiency with type V phenotype (disorder)
\Measurement finding outside reference range\Lipids outside reference range\Lipid above reference range\Hyperlipidemia (disorder)\Hypertriglyceridaemia\Primary hypertriglyceridaemia\Familial hypertriglyceridemia\Familial hyperchylomicronemia (disorder)\Familial lipoprotein lipase deficiency with type V phenotype (disorder)

\Disease\Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Disorder of lipoprotein storage and metabolism\Hyperlipidemia (disorder)\Hypertriglyceridaemia\Primary hypertriglyceridaemia\Familial hypertriglyceridemia\Familial hyperchylomicronemia (disorder)\Familial lipoprotein lipase deficiency with type V phenotype (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Familial lipoprotein lipase deficiency with type V phenotype (disorder)	Is a	Familial hyperchylomicronemia (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial lipoprotein lipase deficiency with type V phenotype (disorder)	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial lipoprotein lipase deficiency with type V phenotype (disorder)	Has definitional manifestation	Serum lipids above reference range (finding)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial lipoprotein lipase deficiency with type V phenotype (disorder)	Has definitional manifestation	Lipid above reference range	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial lipoprotein lipase deficiency with type V phenotype (disorder)	Has interpretation	Above reference range	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Familial lipoprotein lipase deficiency with type V phenotype (disorder)	Interprets	Lipids measurement (procedure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
1771754012	Familial lipoprotein lipase deficiency with type V phenotype (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1782835012	Familial lipoprotein lipase deficiency with type V phenotype	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1771754012	Familial lipoprotein lipase deficiency with type V phenotype (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1782835012	Familial lipoprotein lipase deficiency with type V phenotype	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
6167231000241114	déficit familial en lipoprotéine lipase avec phénotype de type V	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6167241000241116	déficit familial en LPL (lipoprotéine lipase) avec phénotype de type V	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6167231000241114	déficit familial en lipoprotéine lipase avec phénotype de type V	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6167241000241116	déficit familial en LPL (lipoprotéine lipase) avec phénotype de type V	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module