403827000: Familial lipoprotein lipase deficiency with type I 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\Hypertriglyceridaemia\Primary hypertriglyceridaemia\Familial hypertriglyceridemia\Familial hyperchylomicronemia\Familial lipoprotein lipase deficiency with type I phenotype (disorder)

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

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

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

Descriptions:

Id Description Lang Type Status Case? Module

1771753018 Familial lipoprotein lipase deficiency with type I phenotype (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

1782834011 Familial lipoprotein lipase deficiency with type I phenotype en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

1783801016 Familial type I hyperlipoproteinaemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

1784187010 Familial type I hyperlipoproteinemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

974821000052110 familjär lioproteinlipasbrist, fenotyp 1 sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

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

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets