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1204167003: Catecholaminergic polymorphic ventricular tachycardia due to calsequestrin mutation (disorder)


Status: current, Primitive. Date: 31-Mar 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4970045015 Catecholaminergic polymorphic ventricular tachycardia due to calsequestrin mutation (disorder) en Fully specified name Active Case insensitive SNOMED CT core
4970046019 Catecholaminergic polymorphic ventricular tachycardia due to calsequestrin mutation en Synonym Active 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 calsequestrin mutation Is a Catecholaminergic polymorphic ventricular tachycardia true Inferred relationship Some
Catecholaminergic polymorphic ventricular tachycardia due to calsequestrin mutation Finding site Ventricular conducting pathway true Inferred relationship Some 2
Catecholaminergic polymorphic ventricular tachycardia due to calsequestrin mutation Interprets Heart rate true Inferred relationship Some 1
Catecholaminergic polymorphic ventricular tachycardia due to calsequestrin mutation Has interpretation Increased true Inferred relationship Some 1
Catecholaminergic polymorphic ventricular tachycardia due to calsequestrin mutation Is a Cardiac complication true Inferred relationship Some
Catecholaminergic polymorphic ventricular tachycardia due to calsequestrin mutation Due to Chromosomal disorder true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Cardiovascular finding reference set

Problem/Diagnosis reference set

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