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402787000: Primary genetic mixed 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
1770711013 Primary genetic mixed hyperlipidemia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
1773670010 Primary genetic mixed hyperlipidaemia en Synonym Active Entire term case insensitive SNOMED CT core module
1774956015 Primary genetic mixed hyperlipidemia en Synonym Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

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