Phenotypes for disease #03905 (MDDGC14;LGMD2T (dystrophy-dystroglycanopathy, muscular, (limb-girdle), type C14 (LGMD2T)), OMIM:615352)

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AscendingPhenotype ID     

Phenotype details     

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Individual ID     
0000357038 Myopathy, reduced muscle fiber alpha dystroglycan, Intellectual disability mild, elevated serum creatinine kinase Alphadystroglycanopathy Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development) Unknown - - - - - Camille Verebi 00472229
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