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402785008: Primary genetic hyperlipidemia (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
1770709016 Primary genetic hyperlipidemia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
1773669014 Primary genetic hyperlipidaemia en Synonym Active Entire term case insensitive SNOMED CT core module
1774955016 Primary genetic hyperlipidemia en Synonym Active Entire term case insensitive SNOMED CT core module

5 descendants. Search Descendants:

Expanded Value Set

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

This concept is not in any reference sets

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