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 6451 - 6475 of 62743 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Gene Name UniProt ID
C0037939 Spinal Neoplasms ARSA 410 arylsulfatase A P15289
C0020676 Hypothyroidism ARSA 410 arylsulfatase A P15289
C0026709 Mucopolysaccharidosis VI ARSB 411 arylsulfatase B P15848
C1306459 Primary malignant neoplasm ARSB 411 arylsulfatase B P15848
C0010674 Cystic Fibrosis ARSB 411 arylsulfatase B P15848
C0023522 Leukodystrophy, Metachromatic ARSB 411 arylsulfatase B P15848
C0027059 Myocarditis ARSB 411 arylsulfatase B P15848
C0085078 Lysosomal Storage Diseases ARSB 411 arylsulfatase B P15848
C0002986 Fabry Disease ARSB 411 arylsulfatase B P15848
C0026707 Mucopolysaccharidosis IV ARSB 411 arylsulfatase B P15848
C0020538 Hypertensive disease ARSB 411 arylsulfatase B P15848
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

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Last updated: August 19, 2024