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| Term | autosomal recessive limb-girdle muscular dystrophy type 2G | ID (Ontology) | DOID:0110281 (Human Disease) |
| Definition | An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in mutation in the gene encoding telethonin (TCAP). | ||
| Also Known As | "LGMD2G" ; "limb-girdle muscular dystrophy due to telethonin deficiency" ; "muscular dystrophy, limb-girdle, type 2G" | ||
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autosomal recessive disease_____ limb-girdle muscular dystrophy__| autosomal recessive limb-girdle muscular dystrophy |__autosomal recessive limb-girdle muscular dystrophy type 2G |
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| Is a | autosomal recessive limb-girdle muscular dystrophy | ||
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ICD10CM:G71.0 MIM:601954 ORDO:34514 |
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