FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

402474007: Primary polygenic type IIb combined hyperlipidemia (disorder)


Status: current, Primitive. Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4591942015 Primary polygenic type IIb combined hyperlipidemia (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
4591943013 Primary polygenic type IIb combined hyperlipidaemia en Synonym Active Initial character case insensitive SNOMED CT core
4591944019 Primary polygenic type IIb combined hyperlipidemia en Synonym Active Initial character case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

Back to Start