short QT syndrome https://www.malacards.org/card/familial_short_qt_syndrome https://www.malacards.org/card/short_qt_syndrome SCTID:698272007 icd11.foundation:553392015 short QT syndrome MESH:C580439 MONDO:0000453 UMLS:C2348199 GARD:0016650 MEDGEN:378835 Orphanet:51083 NCIT:C71060 DOID:0050793 ICD9:426.89 NORD:2019 OMIMPS:609620 ventricular arrhythmia associated with short QT syndrome A genetic disease of the electrical system of the heart that consists of a constellation of signs and symptoms, consisting of a short QT interval on an EKG (< 300 ms) that does not significantly change with heart rate, tall and peaked T waves, and a structurally normal heart. Short QT syndrome appears to be inherited in an autosomal dominant pattern, and a few affected families have been identified heart conduction disease cardiogenetic rhythm disorder