FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term long QT syndrome 16 ID (Ontology) DOID:0070533 (Human Disease)
Definition A long QT syndrome characterized by perinatal onset of markedly prolonged corrected QT (QTc) interval, 2:1 atrioventricular (AV) block, and bradycardia or ventricular tachycardia (torsades de pointes) that has_material_basis_in heterozygous mutation in the CALM3 gene on chromosome 19q13.32. Syncope, cardiac arrest, and sudden death are common.
Also Known As "LQT16"
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 long QT syndrome 16       8
 for disease ribbon | long QT syndrome 16       8
 model of | long QT syndrome 16       8
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autosomal genetic disease
 |__autosomal dominant disease__
intrinsic cardiomyopathy        |
 |__long QT syndrome____________|
                                long QT syndrome 16  8 rec.
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Is a autosomal dominant disease
long QT syndrome
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Synonyms
  • "LQT16" EXACT OMO:0003012
Secondary IDs
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MIM:618782