Phenotypes for disease #05946 (MMYAT (myopathy, mitochondrial, and ataxia (MMYAT)), OMIM:617675)

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AscendingPhenotype ID     

Diagnosis/Initial     

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Phenotype details     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Owner     

Individual ID     
0000357006 Metabolic myopathy Myopathy, mitochondrial, and ataxia EMG abnormality * Increased muscle glycogen content * Type 1 muscle fiber predominance * Abnormal circulating creatine kinase concentration * Axial muscle weakness * Pelvic girdle muscle weakness * Shoulder girdle muscle weakness * Exercise-induced muscle stiffness Isolated (sporadic) - - - - Camille Verebi 00472197
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