Symptom Information: Sort according to HPO 

1
 (HPO:0003198) Myopathy 151 / 7739
2
 (OMIM) Carnitine deficiency in muscle 1 / 7739
3
 (HPO:0000007) Autosomal recessive inheritance 2538 / 7739
4
 (HPO:0030362) Reduced muscle carnitine level 2 / 7739