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| Term | arrhythmogenic right ventricular dysplasia 4 | ID (Ontology) | DOID:0110073 (Human Disease) |
| Definition | An arrhythmogenic right ventricular dysplasia associated with variation in the region 2q32.1-q32.3. | ||
| Also Known As | "arrhythmogenic right ventricular cardiomyopathy 4" ; "ARVC4" ; "ARVD4" (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 4 |
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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:602087 |
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