Phenotypes for disease #05266 (LGMDR25;LGMD2X (dystrophy, muscular, limb-girdle, autosomal recessive, type 25 (LGMD2X)), OMIM:616812)

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0000081986 cardiac arrhythmia, limb-girdle muscular dystrophy - - Familial, autosomal recessive - - - - Johan den Dunnen 00104044
0000081987 see paper; ..., both sibs met early motor milestones; 5y both developed proximal weakness, with calf hypertrophy, macroglossia; weakness progressed to severe quadriparesis; 12y-both siblings required manual wheelchair and motorized wheelchair at 19y - - Familial, autosomal recessive - - - - Johan den Dunnen 00104045
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