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1204129001: catecholaminerge polymorfe ventriculaire tachycardie door RYR2-mutatie (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 Only initial character case insensitive (core metadata concept) SNOMED CT core
4952428012 Catecholaminergic polymorphic ventricular tachycardia due to RYR2 mutation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
13582831000146113 CPVT door RYR2-mutatie nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13582841000146117 catecholaminerge polymorfe ventriculaire tachycardie door RYR2-mutatie (aandoening) nl Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13582851000146119 catecholaminerge polymorfe ventriculaire tachycardie door RYR2-mutatie nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Catecholaminergic polymorphic ventricular tachycardia due to RYR2 mutation (disorder) Is a Cardiac complication true Inferred relationship Some
Catecholaminergic polymorphic ventricular tachycardia due to RYR2 mutation (disorder) Is a Catecholaminergic polymorphic ventricular tachycardia (disorder) true Inferred relationship Some
Catecholaminergic polymorphic ventricular tachycardia due to RYR2 mutation (disorder) Due to Chromosomal disorder (disorder) true Inferred relationship Some 3
Catecholaminergic polymorphic ventricular tachycardia due to RYR2 mutation (disorder) Finding site Structure of ventricular conducting pathway (body structure) true Inferred relationship Some 2
Catecholaminergic polymorphic ventricular tachycardia due to RYR2 mutation (disorder) Interprets Heart rate true Inferred relationship Some 1
Catecholaminergic polymorphic ventricular tachycardia due to RYR2 mutation (disorder) Has interpretation Increased true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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