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| Term | arrhythmogenic right ventricular dysplasia 1 | ID (Ontology) | DOID:0110070 (Human Disease) |
| Definition | An arrhythmogenic right ventricular dysplasia that has_material_basis_in heterozygous mutation in the TGFB3 gene on chromosome 14q24. | ||
| Also Known As | "arrhythmogenic right ventricular cardiomyopathy 1" ; "ARVC1" ; "Uhl anomaly" | ||
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| Records annotated with this term OR any of its CHILD TERMS | |||
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 | |__arrhythmogenic right ventricular cardiomyopathy__| arrhythmogenic right ventricular dysplasia 1 3 rec. |
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| Is a |
arrhythmogenic right ventricular cardiomyopathy autosomal dominant disease |
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External Crossreferences & Linkouts
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ICD10CM:I42.8 ICD10CM:Q24.8 MESH:C536932 MIM:107970 |
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