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Agent Commons
Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
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Hereditary disease
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Familial long QT syndrome
Long QT syndrome 16
rare
Identifiers
MONDO:0032915
OMIM:618782
Part of
Catecholaminergic polymorphic ventricular tachycardia
Familial long QT syndrome
Also known as
LQT16
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