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 3 ID (Ontology) DOID:0110646 (Human Disease)
Definition A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SCN5A gene on chromosome 3p22.2.
Also Known As "LQT3"
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 Genes
 long QT syndrome 3       2
 for disease ribbon | long QT syndrome 3       2
 model of | long QT syndrome 3       2
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease__
intrinsic cardiomyopathy        |
 |__long QT syndrome____________|
polygenic disease               |
 |__digenic disease_____________|
                                long QT syndrome 3  2 rec.
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Is a autosomal dominant disease
digenic disease
long QT syndrome
Part of
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Synonyms
  • "LQT3" EXACT OMO:0003012
Secondary IDs
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GARD:3286
ICD10CM:I45.8
MESH:C565840
MIM:603830