402785008: Primary genetic hyperlipidemia (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)\Endogenous hyperlipidaemia\Primary genetic hyperlipidemia (disorder)

\Measurement finding outside reference range\Measurement finding above reference range (finding)\Lipid above reference range\Hyperlipidemia (disorder)\Endogenous hyperlipidaemia\Primary genetic hyperlipidemia (disorder)
\Measurement finding outside reference range\Lipids outside reference range\Lipid above reference range\Hyperlipidemia (disorder)\Endogenous hyperlipidaemia\Primary genetic hyperlipidemia (disorder)

\Disease\Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Disorder of lipoprotein storage and metabolism\Hyperlipidemia (disorder)\Endogenous hyperlipidaemia\Primary genetic hyperlipidemia (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

1770709016 Primary genetic hyperlipidemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

1773669014 Primary genetic hyperlipidaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

1774955016 Primary genetic hyperlipidemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

1770709016 Primary genetic hyperlipidemia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

1770709016 Primary genetic hyperlipidemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

1773669014 Primary genetic hyperlipidaemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

1773669014 Primary genetic hyperlipidaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

1774955016 Primary genetic hyperlipidemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

1774955016 Primary genetic hyperlipidemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

5261581000241119 hyperlipidémie génétique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

5261581000241119 hyperlipidémie génétique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Primary genetic hyperlipidemia (disorder)	Is a	Endogenous hyperlipidaemia	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Primary genetic hyperlipidemia (disorder)	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Primary genetic hyperlipidemia (disorder)	Has definitional manifestation	Serum lipids above reference range (finding)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Primary genetic hyperlipidemia (disorder)	Has definitional manifestation	Lipid above reference range	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Primary genetic hyperlipidemia (disorder)	Interprets	Lipids measurement (procedure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Primary genetic hyperlipidemia (disorder)	Has interpretation	Above reference range	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Chylomicronemia syndrome (disorder)	Is a	True	Primary genetic hyperlipidemia (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Primary genetic mixed hyperlipidaemia	Is a	True	Primary genetic hyperlipidemia (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets