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


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Mar 2022. Module: SNOMED CT core module

Descriptions:

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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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