267435002: Familial hyperchylomicronemia (disorder)

SNOMED CT Concept\constatation clinique\...

\Evaluation finding\Measurement finding\...

\Finding of substance level (finding)\Lipid level - finding\Lipids abnormal\Increased lipid\hyperlipidémie\hypertriglycéridémie\Primary hypertriglyceridaemia\Familial hypertriglyceridaemia\Familial hyperchylomicronemia

\Measurement finding outside reference range\Measurement finding above reference range\Increased lipid\hyperlipidémie\hypertriglycéridémie\Primary hypertriglyceridaemia\Familial hypertriglyceridaemia\Familial hyperchylomicronemia
\Measurement finding outside reference range\Lipids abnormal\Increased lipid\hyperlipidémie\hypertriglycéridémie\Primary hypertriglyceridaemia\Familial hypertriglyceridaemia\Familial hyperchylomicronemia

\Disease\trouble métabolique\troubles du métabolisme des lipoprotéines et/ou des lipides\troubles du stockage et du métabolisme des lipoprotéines\hyperlipidémie\hypertriglycéridémie\Primary hypertriglyceridaemia\Familial hypertriglyceridaemia\Familial hyperchylomicronemia

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

398860018 Hyperchylomicronemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

398861019 Primary hyperchylomicronemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

398862014 Primary hyperchylomicronaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

398863016 Familial hyperchylomicronemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

398865011 Burger-Grutz syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

398867015 Familial hyperchylomicronaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

398868013 Hyperchylomicronaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

660051013 Familial hyperchylomicronemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Familial hyperchylomicronemia	est un(e) (attribut)	Familial hypertriglyceridaemia	true	Inferred relationship	Some
Familial hyperchylomicronemia	est défini par la manifestation de (attribut)	Serum lipids high	false	Inferred relationship	Some
Familial hyperchylomicronemia	est défini par la manifestation de (attribut)	Increased lipid	false	Inferred relationship	Some
Familial hyperchylomicronemia	survenue (attribut)	congénital	false	Inferred relationship	Some
Familial hyperchylomicronemia	localisation d'une constatation (attribut)	structure d'un système corporel	false	Inferred relationship	Some
Familial hyperchylomicronemia	est un(e) (attribut)	Primary hypertriglyceridaemia	false	Inferred relationship	Some
Familial hyperchylomicronemia	interprète (attribut)	Lipids measurement	true	Inferred relationship	Some	1
Familial hyperchylomicronemia	a pour interprétation (attribut)	au-dessus de l'étendue de référence	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
déficit familial en apolipoprotéine C-II (trouble)	est un(e) (attribut)	False	Familial hyperchylomicronemia	Inferred relationship	Some
Familial lipoprotein lipase deficiency with type I phenotype (disorder)	est un(e) (attribut)	True	Familial hyperchylomicronemia	Inferred relationship	Some
Familial lipoprotein lipase deficiency with type V phenotype (disorder)	est un(e) (attribut)	True	Familial hyperchylomicronemia	Inferred relationship	Some

This concept is not in any reference sets