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 40901 - 40925 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0086795 Pfaundler-Hurler Syndrome ARSB 411 arylsulfatase B P15848
C0524620 Metabolic Syndrome X ARSB 411 arylsulfatase B P15848
C0024117 Chronic Obstructive Airway Disease ARSB 411 arylsulfatase B P15848
C0019572 Hirsutism ARSB 411 arylsulfatase B P15848
C1306503 Congenital exomphalos ARSB 411 arylsulfatase B P15848
C0024121 Lung Neoplasms ARSB 411 arylsulfatase B P15848
C0086647 Mucopolysaccharidosis Type IIIA ARSB 411 arylsulfatase B P15848
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

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Last updated: August 19, 2024