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| Term | catecholaminergic polymorphic ventricular tachycardia 5 | ID (Ontology) | DOID:0060679 (Human Disease) |
| Definition | A catecholaminergic polymorphic ventricular tachycardia that is characterized by autosomal recessive inheritance and has_material_basis_in homozygous or compound heterozygous mutation in the TRDN gene on chromosome 6q22. | ||
| Also Known As | "CVPT5" | ||
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monogenic disease_________ heart conduction disease__| catecholaminergic polymorphic ventricular tachycardia |__catecholaminergic polymorphic ventricular tachycardia 5 |
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| Is a | catecholaminergic polymorphic ventricular tachycardia | ||
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ICD10CM:I47.2 MIM:615441 |
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