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 6526 - 6550 of 62743 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Gene Name UniProt ID
C0848558 Hypospadias ARSD 414 arylsulfatase D P51689
C0025362 Mental Retardation ARSD 414 arylsulfatase D P51689
C0004936 Mental disorders ARSD 414 arylsulfatase D P51689
C0013473 Eating Disorders ARSD 414 arylsulfatase D P51689
C0004245 Atrioventricular Block ARSD 414 arylsulfatase D P51689
C0175702 Williams Syndrome ARSD 414 arylsulfatase D P51689
C1263846 Attention deficit hyperactivity disorder ARSD 414 arylsulfatase D P51689
C0016522 Foramen Ovale, Patent ARSD 414 arylsulfatase D P51689
C0014175 Endometriosis ARSD 414 arylsulfatase D P51689
C0018553 Hamartoma Syndrome, Multiple ARSD 414 arylsulfatase D P51689
C1409792 Coronary sinus defect ARSD 414 arylsulfatase D P51689
C0023487 Acute Promyelocytic Leukemia ARSD 414 arylsulfatase D P51689
C0018818 Ventricular Septal Defects ARSD 414 arylsulfatase D P51689
C0010068 Coronary heart disease ARSD 414 arylsulfatase D P51689
C0026010 Microphthalmos ARSD 414 arylsulfatase D P51689
C0034089 Pulmonary Valve Stenosis ARSD 414 arylsulfatase D P51689
C0007789 Cerebral Palsy ARSD 414 arylsulfatase D P51689
C0268548 Hyperargininemia ARSD 414 arylsulfatase D P51689
C0035220 Respiratory Distress Syndrome, Newborn ARSD 414 arylsulfatase D P51689
C0018798 Congenital Heart Defects ARSD 414 arylsulfatase D P51689
C1541923 Infective endocarditis ARSD 414 arylsulfatase D P51689
C0000768 Congenital Abnormality ARSD 414 arylsulfatase D P51689
C0038436 Post-Traumatic Stress Disorder ARSD 414 arylsulfatase D P51689
C4721769 Citrullinemia Type 1 ARSD 414 arylsulfatase D P51689
C0028754 Obesity ARSD 414 arylsulfatase D P51689

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Last updated: August 19, 2024