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402474007: Primary polygenic type IIb combined 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
4591942015 Primary polygenic type IIb combined hyperlipidemia (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
4591943013 Primary polygenic type IIb combined hyperlipidaemia en Synonym Active Only initial character case insensitive SNOMED CT core module
4591944019 Primary polygenic type IIb combined hyperlipidemia en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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