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

GeneID	Gene_Symbol	DisGeNet_diseaseID	Disease_name	DisGeNet score	DisGeNet_sourceDB
410	ARSA	C0023522	Leukodystrophy, Metachromatic	0.555550013600383	BEFREE;CTD_human;GAD;LHGDN;MGD;UNIPROT
410	ARSA	C0001973	Alcoholic Intoxication, Chronic	0.203231208875927	BEFREE;GAD;PSYGENET
410	ARSA	C0751276	Metachromatic leukodystrophy, juvenile type	0.201098907136852	BEFREE;ORPHANET
410	ARSA	C0751279	Metachromatic Leukodystrophy, Adult-Type (disorder)	0.201098907136852	BEFREE;ORPHANET
410	ARSA	C0007758	Cerebellar Ataxia	0.200274726784213	BEFREE;HPO
410	ARSA	C0014544	Epilepsy	0.200274726784213	BEFREE;HPO
410	ARSA	C0041696	Unipolar Depression	0.200274726784213	BEFREE;PSYGENET
410	ARSA	C1269683	Major Depressive Disorder	0.200274726784213	BEFREE;PSYGENET
410	ARSA	C0008325	Cholecystitis	0.2	HPO
410	ARSA	C0008489	Chorea	0.2	HPO
410	ARSA	C0011253	Delusions	0.2	HPO
410	ARSA	C0013362	Dysarthria	0.2	HPO
410	ARSA	C0013421	Dystonia	0.2	HPO
410	ARSA	C0018524	Hallucinations	0.2	HPO
410	ARSA	C0025362	Mental Retardation	0.2	HPO
410	ARSA	C0026827	Muscle hypotonia	0.2	HPO
410	ARSA	C0029124	Optic Atrophy	0.2	HPO
410	ARSA	C0034372	Quadriplegia	0.2	HPO
410	ARSA	C0034935	Babinski Reflex	0.2	HPO
410	ARSA	C0036572	Seizures	0.2	HPO
410	ARSA	C0042024	Urinary Incontinence	0.2	HPO
410	ARSA	C0085633	Mood swings	0.2	HPO
410	ARSA	C0151889	Hyperreflexia	0.2	HPO
410	ARSA	C0232769	Abnormal gallbladder function	0.2	HPO
410	ARSA	C0234985	Mental deterioration	0.2	HPO
410	ARSA	C0235153	Hallucinations, Sensory	0.2	HPO
410	ARSA	C0423903	Low intelligence	0.2	HPO
410	ARSA	C0426970	Spastic Quadriplegia	0.2	HPO
410	ARSA	C0542223	Loss of speech	0.2	HPO
410	ARSA	C0575081	Gait abnormality	0.2	HPO
410	ARSA	C0700078	Decreased tendon reflex	0.2	HPO
410	ARSA	C0878575	Peripheral demyelination	0.2	HPO
410	ARSA	C0917816	Mental deficiency	0.2	HPO
410	ARSA	C0948163	Leukoaraiosis	0.2	HPO
410	ARSA	C1301959	Bulbar weakness	0.2	HPO
410	ARSA	C1806780	Cerebrospinal fluid protein increased above normal	0.2	HPO
410	ARSA	C1843367	Poor school performance	0.2	HPO
410	ARSA	C1857640	Decreased nerve conduction velocity	0.2	HPO
410	ARSA	C1859178	Progressive peripheral neuropathy	0.2	HPO
410	ARSA	C3714756	Intellectual Disability	0.2	HPO
410	ARSA	C4020851	Cortical white matter abnormalities seen on MRI	0.2	HPO
410	ARSA	C4020858	Choreatic disease	0.2	HPO
410	ARSA	C4020871	Dystonic disease	0.2	HPO
410	ARSA	C4020876	Dull intelligence	0.2	HPO
410	ARSA	C4020899	Autosomal recessive predisposition	0.2	HPO
410	ARSA	C4021727	EMG: neuropathic changes	0.2	HPO
410	ARSA	C4082299	Bulbar palsy	0.2	HPO
410	ARSA	C0085078	Lysosomal Storage Diseases	0.005494535684262	BEFREE
410	ARSA	C0751278	Metachromatic Leukodystrophy, Infant	0.0030219946263441	BEFREE
410	ARSA	C0026709	Mucopolysaccharidosis VI	0.00273291246481375	LHGDN
410	ARSA	C0002395	Alzheimer's Disease	0.002407028523288	GAD
410	ARSA	C0013080	Down Syndrome	0.002407028523288	GAD
410	ARSA	C0235031	Neurologic Symptoms	0.0019230874894917	BEFREE
410	ARSA	C0009324	Ulcerative Colitis	0.0016483607052786	BEFREE
410	ARSA	C0268263	Multiple Sulfatase Deficiency Disease	0.0013736339210655	BEFREE
410	ARSA	C0596263	Carcinogenesis	0.0013736339210655	BEFREE
410	ARSA	C0007102	Malignant tumor of colon	0.0010989071368524	BEFREE
410	ARSA	C0009319	Colitis	0.0010989071368524	BEFREE
410	ARSA	C0009402	Colorectal Carcinoma	0.0010989071368524	BEFREE
410	ARSA	C0699790	Colon Carcinoma	0.0010989071368524	BEFREE
410	ARSA	C1527249	Colorectal Cancer	0.0010989071368524	BEFREE
410	ARSA	C2713319	Arylsulfatase A Deficiency	0.0010989071368524	BEFREE
410	ARSA	C0004096	Asthma	0.0008241803526393	BEFREE
410	ARSA	C0524851	Neurodegenerative Disorders	0.0008241803526393	BEFREE
410	ARSA	C0004135	Ataxia Telangiectasia	0.0005494535684262	BEFREE
410	ARSA	C0021390	Inflammatory Bowel Diseases	0.0005494535684262	BEFREE
410	ARSA	C0152025	Polyneuropathy	0.0005494535684262	BEFREE
410	ARSA	C0178874	Tumor Progression	0.0005494535684262	BEFREE
410	ARSA	C0233514	Abnormal behavior	0.0005494535684262	BEFREE
410	ARSA	C1333990	Hereditary Nonpolyposis Colorectal Cancer	0.0005494535684262	BEFREE
410	ARSA	C0000880	Acanthamoeba Keratitis	0.0002747267842131	BEFREE
410	ARSA	C0004936	Mental disorders	0.0002747267842131	BEFREE
410	ARSA	C0006111	Brain Diseases	0.0002747267842131	BEFREE
410	ARSA	C0006142	Malignant neoplasm of breast	0.0002747267842131	BEFREE
410	ARSA	C0007113	Rectal Carcinoma	0.0002747267842131	BEFREE
410	ARSA	C0010054	Coronary Arteriosclerosis	0.0002747267842131	BEFREE
410	ARSA	C0010068	Coronary heart disease	0.0002747267842131	BEFREE
410	ARSA	C0010278	Craniosynostosis	0.0002747267842131	BEFREE
410	ARSA	C0010346	Crohn Disease	0.0002747267842131	BEFREE
410	ARSA	C0012236	DiGeorge Syndrome	0.0002747267842131	BEFREE
410	ARSA	C0014038	Encephalitis	0.0002747267842131	BEFREE
410	ARSA	C0014550	Epilepsies, Myoclonic	0.0002747267842131	BEFREE
410	ARSA	C0017638	Glioma	0.0002747267842131	BEFREE
410	ARSA	C0020473	Hyperlipidemia	0.0002747267842131	BEFREE
410	ARSA	C0025517	Metabolic Diseases	0.0002747267842131	BEFREE
410	ARSA	C0026769	Multiple Sclerosis	0.0002747267842131	BEFREE
410	ARSA	C0027051	Myocardial Infarction	0.0002747267842131	BEFREE
410	ARSA	C0027430	Nasal Polyps	0.0002747267842131	BEFREE
410	ARSA	C0027765	nervous system disorder	0.0002747267842131	BEFREE
410	ARSA	C0029454	Osteopetrosis	0.0002747267842131	BEFREE
410	ARSA	C0030524	Paratuberculosis	0.0002747267842131	BEFREE
410	ARSA	C0031117	Peripheral Neuropathy	0.0002747267842131	BEFREE
410	ARSA	C0036337	Schizoaffective Disorder	0.0002747267842131	BEFREE
410	ARSA	C0036341	Schizophrenia	0.0002747267842131	BEFREE
410	ARSA	C0038013	Ankylosing spondylitis	0.0002747267842131	BEFREE
410	ARSA	C0038454	Cerebrovascular accident	0.0002747267842131	BEFREE
410	ARSA	C0220704	Shprintzen syndrome	0.0002747267842131	BEFREE
410	ARSA	C0220710	Medium-chain acyl-coenzyme A dehydrogenase deficiency	0.0002747267842131	BEFREE
410	ARSA	C0221505	Lesion of brain	0.0002747267842131	BEFREE
410	ARSA	C0221764	CHRONIC PSYCHOSIS	0.0002747267842131	BEFREE
410	ARSA	C0233794	Memory impairment	0.0002747267842131	BEFREE
410	ARSA	C0263338	Chronic urticaria	0.0002747267842131	BEFREE
410	ARSA	C0268547	Argininosuccinic Aciduria	0.0002747267842131	BEFREE
410	ARSA	C0270922	Peripheral demyelinating neuropathy	0.0002747267842131	BEFREE
410	ARSA	C0338106	Adenocarcinoma of colon	0.0002747267842131	BEFREE
410	ARSA	C0392322	Undifferentiated schizophrenia	0.0002747267842131	BEFREE
410	ARSA	C0400966	Non-alcoholic Fatty Liver Disease	0.0002747267842131	BEFREE
410	ARSA	C0543699	ASA intolerant asthma	0.0002747267842131	BEFREE
410	ARSA	C0678222	Breast Carcinoma	0.0002747267842131	BEFREE
410	ARSA	C0751651	Mitochondrial Diseases	0.0002747267842131	BEFREE
410	ARSA	C0751778	Myoclonic Epilepsies, Progressive	0.0002747267842131	BEFREE
410	ARSA	C0751785	Unverricht-Lundborg Syndrome	0.0002747267842131	BEFREE
410	ARSA	C0751870	Heredodegenerative Disorders, Nervous System	0.0002747267842131	BEFREE
410	ARSA	C1263726	Sulfatiduria	0.0002747267842131	BEFREE
410	ARSA	C1855255	Pseudoarylsulfatase A Deficiency	0.0002747267842131	BEFREE
410	ARSA	C1868263	Platelet Aggregation, Spontaneous	0.0002747267842131	BEFREE
410	ARSA	C1956346	Coronary Artery Disease	0.0002747267842131	BEFREE
410	ARSA	C1961099	Precursor T-Cell Lymphoblastic Leukemia-Lymphoma	0.0002747267842131	BEFREE
410	ARSA	C2919796	Glycogen storage disease type Ia	0.0002747267842131	BEFREE
410	ARSA	C2919828	Chronic ulcerative colitis	0.0002747267842131	BEFREE
410	ARSA	C3160718	PARKINSON DISEASE, LATE-ONSET	0.0002747267842131	BEFREE
410	ARSA	C3273225	Hereditary Neurodegenerative Disorder	0.0002747267842131	BEFREE
410	ARSA	C3539878	Triple Negative Breast Neoplasms	0.0002747267842131	BEFREE
410	ARSA	C3854222	Human immunodeficiency virus (HIV) II infection category B1	0.0002747267842131	BEFREE
410	ARSA	C3899988	Autosomal Recessive Disorder	0.0002747267842131	BEFREE