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267435002: Familial hyperchylomicronemia (disorder)

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

398860018 Hyperchylomicronemia en Synonym Active Case insensitive SNOMED CT core
398861019 Primary hyperchylomicronemia en Synonym Active Case insensitive SNOMED CT core
398862014 Primary hyperchylomicronaemia en Synonym Active Case insensitive SNOMED CT core
398863016 Familial hyperchylomicronemia en Synonym Active Case insensitive SNOMED CT core
398864010 Familial lipoprotein lipase deficiency en Synonym Inactive Initial character case insensitive SNOMED CT core
398865011 Burger-Grutz syndrome en Synonym Active Initial character case insensitive SNOMED CT core
398866012 Familial LPL deficiency en Synonym Inactive Initial character case insensitive SNOMED CT core
398867015 Familial hyperchylomicronaemia en Synonym Active Case insensitive SNOMED CT core
398868013 Hyperchylomicronaemia en Synonym Active Case insensitive SNOMED CT core
660051013 Familial hyperchylomicronemia (disorder) en Fully specified name Active Case insensitive SNOMED CT core

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Familial hyperchylomicronaemia	Is a	Familial hypertriglyceridaemia	true	Inferred relationship	Some
Familial hyperchylomicronaemia	Has definitional manifestation	Serum lipids high	false	Inferred relationship	Some
Familial hyperchylomicronaemia	Has definitional manifestation	Lipid above reference range	false	Inferred relationship	Some
Familial hyperchylomicronaemia	Occurrence	Congenital	false	Inferred relationship	Some
Familial hyperchylomicronaemia	Finding site	Body system structure	false	Inferred relationship	Some
Familial hyperchylomicronaemia	Is a	Primary hypertriglyceridaemia	false	Inferred relationship	Some
Familial hyperchylomicronaemia	Interprets	Lipids measurement	true	Inferred relationship	Some	1
Familial hyperchylomicronaemia	Has interpretation	Above reference range	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Familial apolipoprotein C-II deficiency	Is a	False	Familial hyperchylomicronaemia	Inferred relationship	Some
Familial lipoprotein lipase deficiency with type I phenotype	Is a	True	Familial hyperchylomicronaemia	Inferred relationship	Some
Familial lipoprotein lipase deficiency with type V phenotype	Is a	True	Familial hyperchylomicronaemia	Inferred relationship	Some

Reference Sets

Emergency department reference set

Id	Description	Lang	Type	Status	Case?	Module
398860018	Hyperchylomicronemia	en	Synonym	Active	Case insensitive	SNOMED CT core
398861019	Primary hyperchylomicronemia	en	Synonym	Active	Case insensitive	SNOMED CT core
398862014	Primary hyperchylomicronaemia	en	Synonym	Active	Case insensitive	SNOMED CT core
398863016	Familial hyperchylomicronemia	en	Synonym	Active	Case insensitive	SNOMED CT core
398864010	Familial lipoprotein lipase deficiency	en	Synonym	Inactive	Initial character case insensitive	SNOMED CT core
398865011	Burger-Grutz syndrome	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
398866012	Familial LPL deficiency	en	Synonym	Inactive	Initial character case insensitive	SNOMED CT core
398867015	Familial hyperchylomicronaemia	en	Synonym	Active	Case insensitive	SNOMED CT core
398868013	Hyperchylomicronaemia	en	Synonym	Active	Case insensitive	SNOMED CT core
660051013	Familial hyperchylomicronemia (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core