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 39226 - 39250 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0003467 Anxiety ARSD 414 arylsulfatase D P51689
C0175695 Sotos' syndrome ARSD 414 arylsulfatase D P51689
C0025362 Mental Retardation ARSD 414 arylsulfatase D P51689
C0022672 Acute Kidney Tubular Necrosis ARSD 414 arylsulfatase D P51689
C0086132 Depressive Symptoms ARSD 414 arylsulfatase D P51689
C0035222 Respiratory Distress Syndrome, Adult ARSD 414 arylsulfatase D P51689
C0016667 Fragile X Syndrome ARSD 414 arylsulfatase D P51689
C2981140 Glaucoma of childhood ARSD 414 arylsulfatase D P51689
C0013274 Patent ductus arteriosus ARSD 414 arylsulfatase D P51689
C0149654 Conduct Disorder ARSD 414 arylsulfatase D P51689
C0010068 Coronary heart disease ARSD 414 arylsulfatase D P51689
C0023467 Leukemia, Myelocytic, Acute ARSD 414 arylsulfatase D P51689
C1956257 Pulmonary Stenosis ARSD 414 arylsulfatase D P51689
C1409792 Coronary sinus defect ARSD 414 arylsulfatase D P51689
C0000768 Congenital Abnormality ARSD 414 arylsulfatase D P51689
C0038436 Post-Traumatic Stress Disorder ARSD 414 arylsulfatase D P51689
C0003507 Aortic Valve Stenosis ARSD 414 arylsulfatase D P51689
C0023015 Language Disorders ARSD 414 arylsulfatase D P51689
C0035372 Rett Syndrome ARSD 414 arylsulfatase D P51689
C0339573 Glaucoma, Primary Open Angle ARSD 414 arylsulfatase D P51689
C1856113 Mowat-Wilson syndrome ARSD 414 arylsulfatase D P51689
C0018798 Congenital Heart Defects ARSD 414 arylsulfatase D P51689
C0004936 Mental disorders ARSD 414 arylsulfatase D P51689
C0268547 Argininosuccinic Aciduria ARSD 414 arylsulfatase D P51689
C0751265 Learning Disabilities ARSD 414 arylsulfatase D P51689

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Last updated: August 19, 2024