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 1751 - 1775 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0027819 Neuroblastoma GFRA2 2675 GDNF family receptor alpha 2 O00451
C0346647 Malignant neoplasm of pancreas GFRA2 2675 GDNF family receptor alpha 2 O00451
C2239176 Liver carcinoma GFRA2 2675 GDNF family receptor alpha 2 O00451
C4048196 beta-Mannosidosis MANBA 4126 mannosidase beta O00462
C1384666 hearing impairment MANBA 4126 mannosidase beta O00462
C0002985 Angiokeratoma MANBA 4126 mannosidase beta O00462
C0004096 Asthma MANBA 4126 mannosidase beta O00462
C0085078 Lysosomal Storage Diseases MANBA 4126 mannosidase beta O00462
C0028738 Nystagmus MANBA 4126 mannosidase beta O00462
C0009402 Colorectal Carcinoma MANBA 4126 mannosidase beta O00462
C0026769 Multiple Sclerosis MANBA 4126 mannosidase beta O00462
C0494475 Tonic - clonic seizures MANBA 4126 mannosidase beta O00462
C1527304 Allergic Reaction MANBA 4126 mannosidase beta O00462
C0027765 nervous system disorder MANBA 4126 mannosidase beta O00462
C0008312 Primary biliary cirrhosis MANBA 4126 mannosidase beta O00462
C0036202 Sarcoidosis MANBA 4126 mannosidase beta O00462
C0036572 Seizures MANBA 4126 mannosidase beta O00462
C1561643 Chronic Kidney Diseases MANBA 4126 mannosidase beta O00462
C0002986 Fabry Disease MANBA 4126 mannosidase beta O00462
C0037822 Speech Disorders MANBA 4126 mannosidase beta O00462
C1263846 Attention deficit hyperactivity disorder MANBA 4126 mannosidase beta O00462
C3714756 Intellectual Disability MANBA 4126 mannosidase beta O00462
C0008313 Cholangitis, Sclerosing MANBA 4126 mannosidase beta O00462
C0009806 Constipation MANBA 4126 mannosidase beta O00462
C3808739 MYASTHENIC SYNDROME, CONGENITAL, 8 AGRN 375790 agrin O00468

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Last updated: August 19, 2024