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1204129001: Catecholaminergic polymorphic ventricular tachycardia due to RYR2 mutation (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 28-Feb 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4952427019 Catecholaminergic polymorphic ventricular tachycardia due to RYR2 mutation (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
4952428012 Catecholaminergic polymorphic ventricular tachycardia due to RYR2 mutation 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
Catecholaminergic polymorphic ventricular tachycardia due to RYR2 mutation Is a Cardiac complication true Inferred relationship Existential restriction modifier
Catecholaminergic polymorphic ventricular tachycardia due to RYR2 mutation Is a Catecholaminergic polymorphic ventricular tachycardia true Inferred relationship Existential restriction modifier
Catecholaminergic polymorphic ventricular tachycardia due to RYR2 mutation Due to Chromosomal disorder true Inferred relationship Existential restriction modifier 3
Catecholaminergic polymorphic ventricular tachycardia due to RYR2 mutation Finding site Structure of ventricular conducting pathway true Inferred relationship Existential restriction modifier 2
Catecholaminergic polymorphic ventricular tachycardia due to RYR2 mutation Interprets Heart rate true Inferred relationship Existential restriction modifier 1
Catecholaminergic polymorphic ventricular tachycardia due to RYR2 mutation Has interpretation Increased 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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