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402786009: Chylomicronemia syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
1770710014 Chylomicronemia syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
1781879012 Chylomicronemia syndrome en Synonym Active Entire term case insensitive SNOMED CT core module


3 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Chylomicronemia syndrome Is a Primary chylomicronemia true Inferred relationship Existential restriction modifier
Chylomicronemia syndrome Is a Primary genetic hyperlipidemia true Inferred relationship Existential restriction modifier
Chylomicronemia syndrome Finding site Body system structure false Inferred relationship Existential restriction modifier
Chylomicronemia syndrome Has definitional manifestation Serum lipids above reference range false Inferred relationship Existential restriction modifier
Chylomicronemia syndrome Has definitional manifestation Lipid above reference range false Inferred relationship Existential restriction modifier
Chylomicronemia syndrome Has interpretation Above reference range true Inferred relationship Existential restriction modifier 1
Chylomicronemia syndrome Interprets Lipids measurement true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Familial chylomicronemia syndrome Is a True Chylomicronemia syndrome Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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