Symptom Information: Sort according to HPO 

1
(HPO:0009054) Scapuloperoneal myopathy 2 / 7739
2
(OMIM) Facial myopathy 1 / 7739
3
(OMIM) Myopathic electromyography and muscle biopsy 1 / 7739
4
(HPO:0000006) Autosomal dominant inheritance 2518 / 7739
5
(HPO:0003458) EMG: myopathic abnormalities 38 / 7739
6
(HPO:0003677) Slow progression 134 / 7739
7
(HPO:0030319) Weakness of facial musculature 4 / 7739