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| Term | arrhythmogenic right ventricular dysplasia 10 | ID (Ontology) | DOID:0110081 (Human Disease) |
| Definition | An arrhythmogenic right ventricular dysplasia that has_material_basis_in heterozygous mutation in the desmoglein-2 gene (DSG2) on chromosome 18q12. | ||
| Also Known As | "arrhythmogenic right ventricular cardiomyopathy 10" ; "ARVC10" ; "ARVD10" (for all, see Synonyms field below) | ||
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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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No relevant statements available
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autosomal genetic disease |__autosomal dominant disease_______________________ intrinsic cardiomyopathy | |__arrhythmogenic right ventricular cardiomyopathy__| arrhythmogenic right ventricular dysplasia 10 |
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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 MIM:610193 |
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