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| Term | familial restrictive cardiomyopathy 2 | ID (Ontology) | DOID:0111426 (Human Disease) |
| Definition | A restrictive cardiomyopathy that has_material_basis_in variation in a region on chromosome 10q23.3. | ||
| Also Known As | "RCM2" ; "restrictive cardiomyopathy 2" | ||
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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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intrinsic cardiomyopathy |__restrictive cardiomyopathy |__familial restrictive cardiomyopathy 2 |
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| Is a | restrictive cardiomyopathy | ||
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| MIM:609578 | |||