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 41351 - 41375 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0042109 Urticaria ARSA 410 arylsulfatase A P15289
C0031117 Peripheral Neuropathy ARSA 410 arylsulfatase A P15289
C0751651 Mitochondrial Diseases ARSA 410 arylsulfatase A P15289
C0563625 Agnosia for Pain ARSA 410 arylsulfatase A P15289
C0233844 Clumsiness ARSA 410 arylsulfatase A P15289
C0007959 Charcot-Marie-Tooth Disease ARSA 410 arylsulfatase A P15289
C0549473 Thyroid carcinoma ARSA 410 arylsulfatase A P15289
C0020757 Ichthyoses ARSA 410 arylsulfatase A P15289
C0401067 Unilateral inguinal hernia NOS ARSA 410 arylsulfatase A P15289
C0038013 Ankylosing spondylitis ARSA 410 arylsulfatase A P15289
C0027809 Neurilemmoma ARSA 410 arylsulfatase A P15289
C0086543 Cataract ARSA 410 arylsulfatase A P15289
C2919828 Chronic ulcerative colitis ARSA 410 arylsulfatase A P15289
C1527390 Neoplasms, Intracranial ARSA 410 arylsulfatase A P15289
C0008489 Chorea ARSA 410 arylsulfatase A P15289
C1279945 Acute interstitial pneumonia ARSA 410 arylsulfatase A P15289
C0233794 Memory impairment ARSA 410 arylsulfatase A P15289
C1621958 Glioblastoma Multiforme ARSA 410 arylsulfatase A P15289
C0012236 DiGeorge Syndrome ARSA 410 arylsulfatase A P15289
C0403447 Chronic Kidney Insufficiency ARSA 410 arylsulfatase A P15289
C0011269 Dementia, Vascular ARSA 410 arylsulfatase A P15289
C4082299 Bulbar palsy ARSA 410 arylsulfatase A P15289
C0243026 Sepsis ARSA 410 arylsulfatase A P15289
C0014550 Myoclonic Epilepsy ARSA 410 arylsulfatase A P15289
C0004936 Mental disorders ARSA 410 arylsulfatase A P15289

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Last updated: August 19, 2024