Version 0.65
|
review
|
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
|
Sources
- ClinGen
- Expert Review Red
- Other
Phenotypes
- Long Qt Syndrome 11
- OMIM:611820
- Orphanet:101016
|
Level 3: Cardiac arrhythmia
Level 2: Cardiovascular disorders
Version 1.15
|
review
|
Unknown
|
Sources
- Expert Review Removed
- UKGTN
Phenotypes
Tags
|
Version 3.12
Latest signed off version: v3.11
(1 May 2024)
Component of the following Super Panels:
Cardiac arrhythmias
Sudden unexplained death or survivors of a cardiac event
Unexplained death in infancy and sudden unexplained death in childhood
|
review
|
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
|
Sources
- North West GLH
- Emory Genetics Laboratory
- Long QT syndrome (Version 1.5)
Phenotypes
- Long QT syndrome-11 (611820)
- ?Long QT syndrome-11 611820
|
Level 3: Cardiac arrhythmia
Level 2: Cardiovascular disorders
Version 3.8
Latest signed off version: v3.7
(1 May 2024)
Component of the following Super Panels:
Cardiac arrhythmias
Sudden unexplained death or survivors of a cardiac event
Unexplained death in infancy and sudden unexplained death in childhood
|
review
|
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
|
Sources
- South West GLH
- North West GLH
- Expert Review Red
- UKGTN
- Emory Genetics Laboratory
- Illumina TruGenome Clinical Sequencing Services
- Radboud University Medical Center, Nijmegen
- Expert list
Phenotypes
- Long QT syndrome-11 (611820)
- Long QT syndrome-11
|
Version 0.36
|
review
|
Not set
|
Sources
|