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 10 ID (Ontology) DOID:0110651 (Human Disease)
Definition A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SCN4B gene on chromosome 11q23.3.
Also Known As "LQT10"
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autosomal genetic disease
 |__autosomal dominant disease__
intrinsic cardiomyopathy        |
 |__long QT syndrome____________|
                                long QT syndrome 10
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Is a autosomal dominant disease
long QT syndrome
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Synonyms
  • "LQT10" EXACT OMO:0003012
Secondary IDs
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GARD:10436
ICD10CM:I45.8
MESH:C567514
MIM:611819