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 39276 - 39300 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0233794 Memory impairment ARSD 414 arylsulfatase D P51689
C0004245 Atrioventricular Block ARSD 414 arylsulfatase D P51689
C0007222 Cardiovascular Diseases ARSD 414 arylsulfatase D P51689
C0270972 Cornelia De Lange Syndrome ARSD 414 arylsulfatase D P51689
C1541923 Infective endocarditis ARSD 414 arylsulfatase D P51689
C0023186 Learning Disorders ARSD 414 arylsulfatase D P51689
C0878544 Cardiomyopathies ARSD 414 arylsulfatase D P51689
C1510586 Autism Spectrum Disorders ARSD 414 arylsulfatase D P51689
C0678222 Breast Carcinoma ARSD 414 arylsulfatase D P51689
C0344724 Ostium secundum atrial septal defect ARSD 414 arylsulfatase D P51689
C0028043 Nicotine Dependence ARSD 414 arylsulfatase D P51689
C0848558 Hypospadias ARSD 414 arylsulfatase D P51689
C0003076 Aniridia ARSD 414 arylsulfatase D P51689
C0020538 Hypertensive disease ARSD 414 arylsulfatase D P51689
C4721769 Citrullinemia Type 1 ARSD 414 arylsulfatase D P51689
C0007789 Cerebral Palsy ARSD 414 arylsulfatase D P51689
C1853235 Sclerocornea ARSD 414 arylsulfatase D P51689
C0021053 Immune System Diseases ARSD 414 arylsulfatase D P51689
C0018802 Congestive heart failure ARSD 414 arylsulfatase D P51689
C0018818 Ventricular Septal Defects ARSD 414 arylsulfatase D P51689
C0017601 Glaucoma ARSD 414 arylsulfatase D P51689
C0011570 Mental Depression ARSD 414 arylsulfatase D P51689
C0018553 Hamartoma Syndrome, Multiple ARSD 414 arylsulfatase D P51689
C0003469 Anxiety Disorders ARSD 414 arylsulfatase D P51689
C0016522 Foramen Ovale, Patent ARSD 414 arylsulfatase D P51689

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Last updated: August 19, 2024