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

GeneID	Gene_Symbol	DisGeNet_diseaseID	Disease_name	DisGeNet score	DisGeNet_sourceDB
64419	MTMR14	C1834558	Myopathy, Centronuclear, Autosomal Dominant	0.6	CTD_human;ORPHANET;UNIPROT
64419	MTMR14	C0752282	Congenital Structural Myopathy	0.00273291246481375	LHGDN
64419	MTMR14	C0040336	Tobacco Use Disorder	0.002407028523288	GAD
64419	MTMR14	C0015672	Fatigue	0.0002747267842131	BEFREE
64419	MTMR14	C0026848	Myopathy	0.0002747267842131	BEFREE
64419	MTMR14	C0030552	Paresis	0.0002747267842131	BEFREE
64419	MTMR14	C0151786	Muscle Weakness	0.0002747267842131	BEFREE
64419	MTMR14	C0175709	Centronuclear myopathy	0.0002747267842131	BEFREE