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 15001 - 15025 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▲ UniProt ID
C0086132 Depressive Symptoms ARSD 414 arylsulfatase D P51689
C0339573 Glaucoma, Primary Open Angle ARSD 414 arylsulfatase D P51689
C0028043 Nicotine Dependence ARSD 414 arylsulfatase D P51689
C0003507 Aortic Valve Stenosis ARSD 414 arylsulfatase D P51689
C0013080 Down Syndrome ARSD 414 arylsulfatase D P51689
C0020302 Hydrophthalmos ARSD 414 arylsulfatase D P51689
C0032897 Prader-Willi Syndrome ARSD 414 arylsulfatase D P51689
C0236792 Asperger Syndrome ARSD 414 arylsulfatase D P51689
C0023467 Leukemia, Myelocytic, Acute ARSD 414 arylsulfatase D P51689
C0149630 Bicuspid aortic valve ARSD 414 arylsulfatase D P51689
C0032460 Polycystic Ovary Syndrome ARSD 414 arylsulfatase D P51689
C2981140 Glaucoma of childhood ARSD 414 arylsulfatase D P51689
C0018801 Heart failure ARSD 414 arylsulfatase D P51689
C1856113 Mowat-Wilson syndrome ARSD 414 arylsulfatase D P51689
C0018799 Heart Diseases ARSD 414 arylsulfatase D P51689
C0035372 Rett Syndrome ARSD 414 arylsulfatase D P51689
C0007194 Hypertrophic Cardiomyopathy ARSD 414 arylsulfatase D P51689
C0152227 Excessive tearing ARSD 414 arylsulfatase D P51689
C0014116 Endocardial Cushion Defects ARSD 414 arylsulfatase D P51689
C0270972 Cornelia De Lange Syndrome ARSD 414 arylsulfatase D P51689
C1136249 Mental Retardation, X-Linked ARSD 414 arylsulfatase D P51689
C1956257 Pulmonary Stenosis ARSD 414 arylsulfatase D P51689
C0043202 Wolff-Parkinson-White Syndrome ARSD 414 arylsulfatase D P51689
C0024121 Lung Neoplasms ARSF 416 arylsulfatase F P54793
C0021400 Influenza ARSF 416 arylsulfatase F P54793

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Last updated: August 19, 2024