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| Term | long QT syndrome 6 | ID (Ontology) | DOID:0110648 (Human Disease) |
| Definition | A long QT interval syndrome that has_material_basis_in dominant inheritance of mutation in the KCNE2 gene on chromosome 21q22.11. | ||
| Also Known As | "LQT6" | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal genetic disease |__autosomal dominant disease__ intrinsic cardiomyopathy | |__long QT syndrome____________| polygenic disease | |__digenic disease_____________| long QT syndrome 6 |
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| Is a |
autosomal dominant disease digenic disease long QT syndrome |
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External Crossreferences & Linkouts
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GARD:10434 ICD10CM:I45.8 MESH:C566333 MIM:613693 |
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