FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.2  |  FHIR Version n/a  User: [n/a]

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


Status: current, Primitive. Date: 28-Feb 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4952427019 Catecholaminergic polymorphic ventricular tachycardia due to RYR2 mutation (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
4952428012 Catecholaminergic polymorphic ventricular tachycardia due to RYR2 mutation en Synonym Active Initial character case insensitive SNOMED CT core


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 Some
Catecholaminergic polymorphic ventricular tachycardia due to RYR2 mutation Is a Catecholaminergic polymorphic ventricular tachycardia true Inferred relationship Some
Catecholaminergic polymorphic ventricular tachycardia due to RYR2 mutation Due to Chromosomal disorder true Inferred relationship Some 3
Catecholaminergic polymorphic ventricular tachycardia due to RYR2 mutation Finding site Ventricular conducting pathway true Inferred relationship Some 2
Catecholaminergic polymorphic ventricular tachycardia due to RYR2 mutation Interprets Heart rate true Inferred relationship Some 1
Catecholaminergic polymorphic ventricular tachycardia due to RYR2 mutation Has interpretation Increased true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Cardiovascular finding reference set

Problem/Diagnosis reference set

Back to Start