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267435002: Familial hyperchylomicronemia (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
398860018 Hyperchylomicronemia en Synonym Active Entire term case insensitive SNOMED CT core module
398861019 Primary hyperchylomicronemia en Synonym Active Entire term case insensitive SNOMED CT core module
398862014 Primary hyperchylomicronaemia en Synonym Active Entire term case insensitive SNOMED CT core module
398863016 Familial hyperchylomicronemia en Synonym Active Entire term case insensitive SNOMED CT core module
398865011 Burger-Grutz syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module
398867015 Familial hyperchylomicronaemia en Synonym Active Entire term case insensitive SNOMED CT core module
398868013 Hyperchylomicronaemia en Synonym Active Entire term case insensitive SNOMED CT core module
660051013 Familial hyperchylomicronemia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

2 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial hyperchylomicronemia Is a Primary hypertriglyceridemia false Inferred relationship Existential restriction modifier
Familial hyperchylomicronemia Occurrence Congenital false Inferred relationship Existential restriction modifier
Familial hyperchylomicronemia Finding site Body system structure false Inferred relationship Existential restriction modifier
Familial hyperchylomicronemia Is a Familial hypertriglyceridemia true Inferred relationship Existential restriction modifier
Familial hyperchylomicronemia Has definitional manifestation Serum lipids above reference range false Inferred relationship Existential restriction modifier
Familial hyperchylomicronemia Has definitional manifestation Lipid above reference range false Inferred relationship Existential restriction modifier
Familial hyperchylomicronemia Interprets Lipids measurement true Inferred relationship Existential restriction modifier 1
Familial hyperchylomicronemia Has interpretation Above reference range true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Familial apolipoprotein C-II deficiency Is a False Familial hyperchylomicronemia Inferred relationship Existential restriction modifier
Familial lipoprotein lipase deficiency with type I phenotype Is a True Familial hyperchylomicronemia Inferred relationship Existential restriction modifier
Familial lipoprotein lipase deficiency with type V phenotype Is a True Familial hyperchylomicronemia Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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