Symptom Information: Sort according to HPO 

1
(HPO:0001638) Cardiomyopathy 192 / 7739
2
(HPO:0002093) Respiratory insufficiency 410 / 7739
3
(HPO:0003236) Elevated serum creatine phosphokinase 214 / 7739
4
(HPO:0003560) Muscular dystrophy 88 / 7739
5
(HPO:0003701) Proximal muscle weakness 105 / 7739
6
(HPO:0007126) Proximal amyotrophy 29 / 7739
7
(HPO:0011675) Arrhythmia 226 / 7739
8
(OMIM) Muscle weakness and atrophy, proximal 5 / 7739
9
(HPO:0000006) Autosomal dominant inheritance 2518 / 7739
10
(HPO:0003812) Phenotypic variability 129 / 7739
11
(HPO:0011463) Childhood onset 65 / 7739