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 47826 - 47850 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
C0376358 Malignant neoplasm of prostate ARSB 411 arylsulfatase B P15848
C0026703 Mucopolysaccharidoses ARSB 411 arylsulfatase B P15848
C0086651 Mucopolysaccharidosis, MPS-IV-A ARSB 411 arylsulfatase B P15848
C0041296 Tuberculosis ARSB 411 arylsulfatase B P15848
C0006826 Malignant Neoplasms ARSB 411 arylsulfatase B P15848
C0017921 Glycogen storage disease type II ARSB 411 arylsulfatase B P15848
C0342751 Generalized glycogen storage disease of infants ARSB 411 arylsulfatase B P15848
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

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Last updated: August 19, 2024