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471885006: Hypertrophic cardiomyopathy with genetic marker (disorder)


Status: current, Primitive. Date: 31-Jan 2013. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2950982017 Hypertrophic cardiomyopathy with genetic marker (disorder) en Fully specified name Active Case insensitive SNOMED CT core
2950983010 Hypertrophic cardiomyopathy with genetic marker en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hypertrophic cardiomyopathy with genetic marker Is a Hypertrophic cardiomyopathy true Inferred relationship Some
Hypertrophic cardiomyopathy with genetic marker Associated morphology Hypertrophy true Inferred relationship Some 1
Hypertrophic cardiomyopathy with genetic marker Finding site Myocardium structure 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

Australian dialect reference set

Cardiovascular finding reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

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