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| Term | autosomal dominant limb-girdle muscular dystrophy type 1H | ID (Ontology) | DOID:0110303 (Human Disease) |
| Definition | An autosomal dominant limb-girdle muscular dystrophy that has_material_basis_in variation in the region 3p25.1-p23. | ||
| Also Known As | "muscular dystrophy limb-girdle type 1H" | ||
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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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autosomal dominant disease______ limb-girdle muscular dystrophy__| autosomal dominant limb-girdle muscular dystrophy |__autosomal dominant limb-girdle muscular dystrophy type 1H |
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| Is a | autosomal dominant limb-girdle muscular dystrophy | ||
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ICD10CM:G71.0 MIM:613530 ORDO:238755 |
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