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| Term | Miyoshi muscular dystrophy | ID (Ontology) | DOID:0070198 (Human Disease) |
| Definition | A distal myopathy that is characterized by autosomal recessive inheritance of distal muscle weakness in the upper and lower limbs that spares the intrinsic muscles of the hands and has onset in young adulthood. | ||
| Also Known As | "Miyoshi myopathy" | ||
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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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muscular dystrophy |__distal myopathy |__Miyoshi muscular dystrophy 3 rec. |__Miyoshi muscular dystrophy 1 1 rec. |__Miyoshi muscular dystrophy 2 |__Miyoshi muscular dystrophy 3 2 rec. |
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| Is a | distal myopathy | ||
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External Crossreferences & Linkouts
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GARD:9676 MESH:C537480 MIM:PS254130 ORDO:45448 |
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