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 48001 - 48025 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
C0345905 Intrahepatic Cholangiocarcinoma ARSA 410 arylsulfatase A P15289
C0040136 Thyroid Neoplasm ARSA 410 arylsulfatase A P15289
C0024115 Lung diseases ARSA 410 arylsulfatase A P15289
C0037930 Spinal Cord Neoplasms ARSA 410 arylsulfatase A P15289
C0678222 Breast Carcinoma ARSA 410 arylsulfatase A P15289
C0751785 Unverricht-Lundborg Syndrome ARSA 410 arylsulfatase A P15289
C0007115 Malignant neoplasm of thyroid ARSA 410 arylsulfatase A P15289
C0014070 Encephalomyelitis ARSA 410 arylsulfatase A P15289
C0027765 nervous system disorder ARSA 410 arylsulfatase A P15289
C0221069 Anterior Spinal Artery Syndrome ARSA 410 arylsulfatase A P15289
C0036337 Schizoaffective Disorder ARSA 410 arylsulfatase A P15289
C0004096 Asthma ARSA 410 arylsulfatase A P15289
C0281361 Adenocarcinoma of pancreas ARSA 410 arylsulfatase A P15289
C0006111 Brain Diseases ARSA 410 arylsulfatase A P15289
C0019270 Hernia ARSA 410 arylsulfatase A P15289
C0019202 Hepatolenticular Degeneration ARSA 410 arylsulfatase A P15289
C0220704 Shprintzen syndrome ARSA 410 arylsulfatase A P15289
C0812413 Malignant Pleural Mesothelioma ARSA 410 arylsulfatase A P15289
C0021051 Immunologic Deficiency Syndromes ARSA 410 arylsulfatase A P15289
C0936282 Blastoma ARSA 410 arylsulfatase A P15289
C0030567 Parkinson Disease ARSA 410 arylsulfatase A P15289
C2919796 Glycogen storage disease type Ia ARSA 410 arylsulfatase A P15289
C0029124 Optic Atrophy ARSA 410 arylsulfatase A P15289
C1855255 Pseudoarylsulfatase A Deficiency ARSA 410 arylsulfatase A P15289
C0037899 Sphingolipidoses ARSA 410 arylsulfatase A P15289

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Last updated: August 19, 2024