Phenotypes for disease #03445 (MDDGC9;LGMDR16;LGMD2P (dystrophy-dystroglycanopathy, muscular, (limb-girdle), type C9 (LGMDR16, LGMD2P)), OMIM:613818)

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AscendingPhenotype ID     

Phenotype details     

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Individual ID     
0000365056 myalgia, increased CK levels - - Familial, autosomal dominant - - - - - Camille Verebi 00480773
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