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| Term | autosomal recessive limb-girdle muscular dystrophy type 2M | ID (Ontology) | DOID:0110296 (Human Disease) |
| Definition | An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding fukutin (FKTN) on chromosome 9q31. | ||
| Also Known As | "LGMD2M" ; "MDDGC4" ; "muscular dystrophy-dystroglycanopathy (limb-girdle) type C 4" | ||
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autosomal recessive disease_____ limb-girdle muscular dystrophy__| autosomal recessive limb-girdle muscular dystrophy |__autosomal recessive limb-girdle muscular dystrophy type 2M |
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| Is a | autosomal recessive limb-girdle muscular dystrophy | ||
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ICD10CM:G71.0 MIM:611588 ORDO:206554 |
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