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Short QT (SQT) Syndromes

Autosomal DominantIon Channels / MembraneOMIM 609620
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Overview

From WUSTL Neuromuscular

SQT1 ● KCNH2 ; Chromosome 7q36.1; Dominant Allelic disorder: LQT2 SQT2 ● KCNQ1 ; Chromosome 11p15.5-p15.4; Dominant Allelic disorders SQT3 ● KCNJ2 ; Chromosome 17q24.3; Dominant Allelic disorders SQT7 ● SLC4A3 ; Chromosome 2q35; Dominant

OMIM Entries

OMIM #609620OMIM #152427OMIM #609621OMIM #607542OMIM #609622OMIM #600681OMIM #620231OMIM #106195

Related Conditions

Shared genes
Long QT Syndromes
KCNJ2CACNA1CSCN4B

External Resources

WUSTL Neuromuscular
Washington University Disease Center
OMIM
Online Mendelian Inheritance in Man
PubMed
Biomedical Literature
GeneReviews
NCBI Expert-Authored Reviews
Orphanet
Portal for Rare Diseases
NORD
National Organization for Rare Disorders

Data sourced from the Washington University Neuromuscular Disease Center. For clinical use, always refer to primary sources.