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


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 Entire term case insensitive (core metadata concept) SNOMED CT core
4970046019 Catecholaminergic polymorphic ventricular tachycardia due to calsequestrin mutation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
7740371000241118 TV (tachycardie ventriculaire) polymorphe catécholaminergique due à une mutation de la calséquestrine fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
7740381000241116 tachycardie ventriculaire polymorphe catécholaminergique due à une mutation de la calséquestrine fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Catecholaminergic polymorphic ventricular tachycardia due to calsequestrin mutation (disorder) Is a Catecholaminergic polymorphic ventricular tachycardia (disorder) true Inferred relationship Some
Catecholaminergic polymorphic ventricular tachycardia due to calsequestrin mutation (disorder) Finding site Ventricular conducting pathway true Inferred relationship Some 2
Catecholaminergic polymorphic ventricular tachycardia due to calsequestrin mutation (disorder) Interprets Heart rate true Inferred relationship Some 1
Catecholaminergic polymorphic ventricular tachycardia due to calsequestrin mutation (disorder) Has interpretation Increased true Inferred relationship Some 1
Catecholaminergic polymorphic ventricular tachycardia due to calsequestrin mutation (disorder) Is a Cardiac complication true Inferred relationship Some
Catecholaminergic polymorphic ventricular tachycardia due to calsequestrin mutation (disorder) Due to Chromosomal disorder (disorder) true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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