Symptom Information: Sort according to HPO 

1
(HPO:0001270) Motor delay 322 / 7739
2
(HPO:0003236) Elevated serum creatine phosphokinase 214 / 7739
3
(HPO:0003560) Muscular dystrophy 88 / 7739
4
(HPO:0001252) Muscular hypotonia 990 / 7739
5
(HPO:0001324) Muscle weakness 859 / 7739
6
(HPO:0008947) Infantile muscular hypotonia 482 / 7739
7
(HPO:0010547) Muscle flaccidity 466 / 7739
8
(OMIM) Muscle biopsy shows decreased glycosylation of alpha-dystroglycan 9 / 7739
9
(HPO:0000007) Autosomal recessive inheritance 2538 / 7739
10
(HPO:0003593) Infantile onset 249 / 7739
11
(HPO:0003741) Congenital muscular dystrophy 22 / 7739