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 6476 - 6500 of 62743 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Gene Name UniProt ID
C0017601 Glaucoma ARSB 411 arylsulfatase B P15848
C0027543 Avascular necrosis of bone ARSB 411 arylsulfatase B P15848
C0009402 Colorectal Carcinoma ARSB 411 arylsulfatase B P15848
C0600139 Prostate carcinoma ARSB 411 arylsulfatase B P15848
C0392476 Epiphyseal dysplasia ARSB 411 arylsulfatase B P15848
C0018802 Congestive heart failure ARSB 411 arylsulfatase B P15848
C0003850 Arteriosclerosis ARSB 411 arylsulfatase B P15848
C0007682 CNS disorder ARSB 411 arylsulfatase B P15848
C0024408 Machado-Joseph Disease ARSB 411 arylsulfatase B P15848
C0004153 Atherosclerosis ARSB 411 arylsulfatase B P15848
C1384666 hearing impairment ARSB 411 arylsulfatase B P15848
C0018801 Heart failure ARSB 411 arylsulfatase B P15848
C0085660 Aseptic necrosis ARSB 411 arylsulfatase B P15848
C0878544 Cardiomyopathies ARSB 411 arylsulfatase B P15848
C0037926 Compression of spinal cord ARSB 411 arylsulfatase B P15848
C0023786 Mucopolysaccharidosis I ARSB 411 arylsulfatase B P15848
C0013336 Dwarfism ARSB 411 arylsulfatase B P15848
C0033975 Psychotic Disorders ARSB 411 arylsulfatase B P15848
C0025202 melanoma ARSB 411 arylsulfatase B P15848
C0019294 Hernia, Inguinal ARSB 411 arylsulfatase B P15848
C0026706 Mucopolysaccharidosis III ARSB 411 arylsulfatase B P15848
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

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Last updated: August 19, 2024