* We recommend a score >= 0.08 for meaningful Gene-Disease associations

GeneID	Gene_Symbol	DisGeNet_diseaseID	Disease_name	DisGeNet score	DisGeNet_sourceDB
5224	PGAM2	C0268149	Glycogen storage disease type X	0.600824180352639	BEFREE;CTD_human;ORPHANET;UNIPROT
5224	PGAM2	C0026848	Myopathy	0.200274726784213	BEFREE;HPO
5224	PGAM2	C0027080	Myoglobinuria	0.2	HPO
5224	PGAM2	C0033578	Prostatic Neoplasms	0.2	CTD_human
5224	PGAM2	C0035078	Kidney Failure	0.2	HPO
5224	PGAM2	C0035410	Rhabdomyolysis	0.2	HPO
5224	PGAM2	C0151576	Elevated creatine kinase	0.2	HPO
5224	PGAM2	C0241005	Creatine phosphokinase serum increased	0.2	HPO
5224	PGAM2	C0424551	Impaired exercise tolerance	0.2	HPO
5224	PGAM2	C1565489	Renal Insufficiency	0.2	HPO
5224	PGAM2	C1839604	Renal failure in adulthood	0.2	HPO
5224	PGAM2	C1850830	Exercise-induced myalgia	0.2	HPO
5224	PGAM2	C1855578	Muscle cramps with exertion	0.2	HPO
5224	PGAM2	C4020899	Autosomal recessive predisposition	0.2	HPO
5224	PGAM2	C0017919	Glycogen Storage Disease	0.0002747267842131	BEFREE
5224	PGAM2	C0270984	Metabolic myopathy	0.0002747267842131	BEFREE