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(HPO:0000006) | Autosomal dominant inheritance | 2518 / 7739 | ||||
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(HPO:0003198) | Myopathy | 151 / 7739 | ||||
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(HPO:0003701) | Proximal muscle weakness | 105 / 7739 | ||||
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(HPO:0003805) | Rimmed vacuoles | 22 / 7739 | ||||
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(HPO:0006785) | Limb-girdle muscular dystrophy | 14 / 7739 | ||||
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(HPO:0008180) | Mildly elevated creatine phosphokinase | 28 / 7739 | ||||
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(HPO:0010991) | Abnormality of the abdominal musculature | 1 / 7739 | ||||
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(HPO:0100299) | Muscle fiber inclusion bodies | 3 / 7739 |