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 40076 - 40100 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▲ UniProt ID
C0006826 Malignant Neoplasms MANEA 79694 mannosidase endo-alpha Q5SRI9
C0003469 Anxiety Disorders MANEA 79694 mannosidase endo-alpha Q5SRI9
C0004936 Mental disorders MANEA 79694 mannosidase endo-alpha Q5SRI9
C1456784 Paranoia MANEA 79694 mannosidase endo-alpha Q5SRI9
C0009171 Cocaine Abuse MANEA 79694 mannosidase endo-alpha Q5SRI9
C0030319 Panic Disorder MANEA 79694 mannosidase endo-alpha Q5SRI9
C0004364 Autoimmune Diseases MANEA 79694 mannosidase endo-alpha Q5SRI9
C1136382 Sclerocystic Ovaries MANEA 79694 mannosidase endo-alpha Q5SRI9
C0006142 Malignant neoplasm of breast MANEA 79694 mannosidase endo-alpha Q5SRI9
C0031572 Phobia, Social MANEA 79694 mannosidase endo-alpha Q5SRI9
C0032460 Polycystic Ovary Syndrome MANEA 79694 mannosidase endo-alpha Q5SRI9
C1541923 Infective endocarditis MANEA 79694 mannosidase endo-alpha Q5SRI9
C0600427 Cocaine Dependence MANEA 79694 mannosidase endo-alpha Q5SRI9
C1306459 Primary malignant neoplasm MANEA 79694 mannosidase endo-alpha Q5SRI9
C0027765 nervous system disorder MANEAL 149175 mannosidase endo-alpha like Q5VSG8
C0524851 Neurodegenerative Disorders MANEAL 149175 mannosidase endo-alpha like Q5VSG8
C2677590 Congenital Disorder Of Glycosylation, Type In MOGS 7841 mannosyl-oligosaccharide glucosidase Q13724
C0018784 Sensorineural Hearing Loss (disorder) MOGS 7841 mannosyl-oligosaccharide glucosidase Q13724
C0036572 Seizures MOGS 7841 mannosyl-oligosaccharide glucosidase Q13724
C0282577 Congenital Disorders of Glycosylation MOGS 7841 mannosyl-oligosaccharide glucosidase Q13724
C0005744 Blepharophimosis MOGS 7841 mannosyl-oligosaccharide glucosidase Q13724
C1367554 Adamantinoma MOGS 7841 mannosyl-oligosaccharide glucosidase Q13724
C1853736 Congenital Disorder Of Glycosylation, Type IIB MOGS 7841 mannosyl-oligosaccharide glucosidase Q13724
C0235946 Cerebral atrophy MOGS 7841 mannosyl-oligosaccharide glucosidase Q13724
C0276289 Zika Virus Infection MOGS 7841 mannosyl-oligosaccharide glucosidase Q13724

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Last updated: August 19, 2024