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

GeneID	Gene_Symbol	DisGeNet_diseaseID	Disease_name	DisGeNet score	DisGeNet_sourceDB
3745	KCNB1	C0543888	Epileptic encephalopathy	0.200824180352639	BEFREE;HPO
3745	KCNB1	C0557874	Global developmental delay	0.200274726784213	BEFREE;HPO
3745	KCNB1	C0019284	Diaphragmatic Hernia	0.2	CTD_human
3745	KCNB1	C0026827	Muscle hypotonia	0.2	HPO
3745	KCNB1	C0684276	Hypsarrhythmia	0.2	HPO
3745	KCNB1	C1848924	Infantile onset	0.2	HPO
3745	KCNB1	C1864897	Cognitive delay	0.2	HPO
3745	KCNB1	C4015119	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 26	0.2	UNIPROT
3745	KCNB1	C4020875	Mental and motor retardation	0.2	HPO
3745	KCNB1	C0020538	Hypertensive disease	0.002407028523288	GAD
3745	KCNB1	C0040336	Tobacco Use Disorder	0.002407028523288	GAD
3745	KCNB1	C0149721	Left Ventricular Hypertrophy	0.002407028523288	GAD
3745	KCNB1	C0002395	Alzheimer's Disease	0.0002747267842131	BEFREE
3745	KCNB1	C0011860	Diabetes Mellitus, Non-Insulin-Dependent	0.0002747267842131	BEFREE
3745	KCNB1	C0014544	Epilepsy	0.0002747267842131	BEFREE
3745	KCNB1	C0023976	Long QT Syndrome	0.0002747267842131	BEFREE
3745	KCNB1	C0036341	Schizophrenia	0.0002747267842131	BEFREE
3745	KCNB1	C0234533	Generalized seizures	0.0002747267842131	BEFREE
3745	KCNB1	C0442874	Neuropathy	0.0002747267842131	BEFREE
3745	KCNB1	C1535926	Neurodevelopmental Disorders	0.0002747267842131	BEFREE
3745	KCNB1	C3887505	DYSFUNCTION - SKIN DISORDERS	0.0002747267842131	BEFREE