TRDN

triadin
OMIM: 603283, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Amber TRDN in Long QT syndrome

Level 3: Cardiac arrhythmia
Level 2: Cardiovascular disorders
Version 2.22
Latest signed off version: v2.20 (20 Aug 2020)

Component of the following Super Panels:

  • Cardiac arrhythmias
  • Sudden cardiac death
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Expert list
    Phenotypes
    • Long QT syndrome
    Tags
    • for-review

    Green TRDN in Catecholaminergic polymorphic VT

    Level 3: Cardiac arrhythmia
    Level 2: Cardiovascular disorders
    Version 2.18
    Latest signed off version: v2.5 (20 Aug 2020)

    Component of the following Super Panels:

  • Cardiac arrhythmias
  • Sudden cardiac death
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • South West GLH
    • London South GLH
    • North West GLH
    • Expert Review Green
    • UKGTN
    • Expert list
    • Radboud University Medical Center, Nijmegen
    • Illumina TruGenome Clinical Sequencing Services
    Phenotypes
    • Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness, OMIM:615441

    Amber TRDN in Congenital myopathy

    Level 3: Neuromuscular disorders
    Level 2: Neurology and neurodevelopmental disorders
    Version 2.28
    Latest signed off version: v2.2 (2 Mar 2020)

    Component of the following Super Panels:

  • Hypotonic infant
  • Neuromuscular disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • NHS GMS
    • Expert Review Amber
    • Expert list
    Phenotypes
    • Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness, 615441