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

GeneID	Gene_Symbol	DisGeNet_diseaseID	Disease_name	DisGeNet score	DisGeNet_sourceDB
1759	DNM1	C0036341	Schizophrenia	0.20328236603324	BEFREE;LHGDN;PSYGENET
1759	DNM1	C0036572	Seizures	0.201098907136852	BEFREE;HPO
1759	DNM1	C0014544	Epilepsy	0.200824180352639	BEFREE;HPO
1759	DNM1	C0543888	Epileptic encephalopathy	0.200549453568426	BEFREE;HPO
1759	DNM1	C0085584	Encephalopathies	0.200274726784213	BEFREE;HPO
1759	DNM1	C1843367	Poor school performance	0.2	HPO
1759	DNM1	C0494475	Tonic - clonic seizures	0.2	HPO
1759	DNM1	C0595948	Atypical absence seizure	0.2	HPO
1759	DNM1	C0746940	nonverbal	0.2	HPO
1759	DNM1	C0856975	Autistic behavior	0.2	HPO
1759	DNM1	C0917816	Mental deficiency	0.2	HPO
1759	DNM1	C1457883	Aggressive reaction	0.2	HPO
1759	DNM1	C1510586	Autism Spectrum Disorders	0.2	HPO
1759	DNM1	C1836508	Hypertonic seizures	0.2	HPO
1759	DNM1	C1836509	Hypotonic seizures	0.2	HPO
1759	DNM1	C1836550	Loss of developmental milestones	0.2	HPO
1759	DNM1	C1836830	Developmental regression	0.2	HPO
1759	DNM1	C3714756	Intellectual Disability	0.2	HPO
1759	DNM1	C1850493	Psychomotor regression, progressive	0.2	HPO
1759	DNM1	C4225357	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 31	0.2	UNIPROT
1759	DNM1	C4023479	EEG with focal sharp slow waves	0.2	HPO
1759	DNM1	C1850601	Brainstem abnormalities	0.2	HPO
1759	DNM1	C1854882	Absent speech	0.2	HPO
1759	DNM1	C1855009	Psychomotor regression in infants	0.2	HPO
1759	DNM1	C1855019	Psychomotor regression	0.2	HPO
1759	DNM1	C1855996	Psychomotor regression beginning in infancy	0.2	HPO
1759	DNM1	C1857121	Neurodevelopmental regression	0.2	HPO
1759	DNM1	C1859678	Mental deterioration in childhood	0.2	HPO
1759	DNM1	C4020876	Dull intelligence	0.2	HPO
1759	DNM1	C0424323	Physical aggression	0.2	HPO
1759	DNM1	C0001807	Aggressive behavior	0.2	HPO
1759	DNM1	C0424295	Hyperactive behavior	0.2	HPO
1759	DNM1	C0423903	Low intelligence	0.2	HPO
1759	DNM1	C0311394	Difficulty walking	0.2	HPO
1759	DNM1	C0270846	Epileptic drop attack	0.2	HPO
1759	DNM1	C0238111	Lennox-Gastaut syndrome	0.2	ORPHANET
1759	DNM1	C0234985	Mental deterioration	0.2	HPO
1759	DNM1	C0025362	Mental Retardation	0.2	HPO
1759	DNM1	C0026827	Muscle hypotonia	0.2	HPO
1759	DNM1	C0031212	Personality Disorders	0.2	HPO
1759	DNM1	C0027066	Myoclonus	0.2	HPO
1759	DNM1	C0270850	Idiopathic generalized epilepsy	0.08	MGD
1759	DNM1	C0010823	Cytomegalovirus Infections	0.00273291246481375	LHGDN
1759	DNM1	C0040336	Tobacco Use Disorder	0.002407028523288	GAD
1759	DNM1	C0002395	Alzheimer's Disease	0.0008241803526393	BEFREE
1759	DNM1	C0028043	Nicotine Dependence	0.0002747267842131	BEFREE
1759	DNM1	C0035369	Retroviridae Infections	0.0002747267842131	BEFREE
1759	DNM1	C0037769	West Syndrome	0.0002747267842131	BEFREE
1759	DNM1	C0017205	Gaucher Disease	0.0002747267842131	BEFREE
1759	DNM1	C1865349	Ethylmalonic encephalopathy	0.0002747267842131	BEFREE
1759	DNM1	C0341106	Eosinophilic esophagitis	0.0002747267842131	BEFREE
1759	DNM1	C3887898	Infantile Spasm	0.0002747267842131	BEFREE
1759	DNM1	C0007959	Charcot-Marie-Tooth Disease	0.0002747267842131	BEFREE
1759	DNM1	C0002726	Amyloidosis	0.0002747267842131	BEFREE
1759	DNM1	C0748607	Recurrent seizures	0.0002747267842131	BEFREE