DisGeNET

DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.

Source Last Updated
DisGeNET July 29, 2024
Displaying entries 14926 - 14950 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▲ UniProt ID
C0020255 Hydrocephalus ARSB 411 arylsulfatase B P15848
C0577631 Carotid Atherosclerosis ARSB 411 arylsulfatase B P15848
C0035222 Respiratory Distress Syndrome, Adult ARSD 414 arylsulfatase D P51689
C0004352 Autistic Disorder ARSD 414 arylsulfatase D P51689
C1510586 Autism Spectrum Disorders ARSD 414 arylsulfatase D P51689
C0003467 Anxiety ARSD 414 arylsulfatase D P51689
C0036341 Schizophrenia ARSD 414 arylsulfatase D P51689
C0149654 Conduct Disorder ARSD 414 arylsulfatase D P51689
C0751265 Learning Disabilities ARSD 414 arylsulfatase D P51689
C0233794 Memory impairment ARSD 414 arylsulfatase D P51689
C0265326 Bannayan-Riley-Ruvalcaba Syndrome ARSD 414 arylsulfatase D P51689
C0023434 Chronic Lymphocytic Leukemia ARSD 414 arylsulfatase D P51689
C0016667 Fragile X Syndrome ARSD 414 arylsulfatase D P51689
C0175683 Citrullinemia ARSD 414 arylsulfatase D P51689
C0003469 Anxiety Disorders ARSD 414 arylsulfatase D P51689
C3714756 Intellectual Disability ARSD 414 arylsulfatase D P51689
C0013274 Patent ductus arteriosus ARSD 414 arylsulfatase D P51689
C0270549 Generalized Anxiety Disorder ARSD 414 arylsulfatase D P51689
C0014121 Bacterial Endocarditis ARSD 414 arylsulfatase D P51689
C1853235 Sclerocornea ARSD 414 arylsulfatase D P51689
C0014544 Epilepsy ARSD 414 arylsulfatase D P51689
C0013170 Drug habituation ARSD 414 arylsulfatase D P51689
C0344315 Depressed mood ARSD 414 arylsulfatase D P51689
C0018817 Atrial Septal Defects ARSD 414 arylsulfatase D P51689
C0021053 Immune System Diseases ARSD 414 arylsulfatase D P51689

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Last updated: August 19, 2024