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 13051 - 13075 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Gene Name UniProt ID
C1851413 EXOSTOSES, MULTIPLE, TYPE II EXT2 2132 exostosin glycosyltransferase 2 Q93063
C0015306 Hereditary Multiple Exostoses EXT2 2132 exostosin glycosyltransferase 2 Q93063
C1868598 PARIETAL FORAMINA EXT2 2132 exostosin glycosyltransferase 2 Q93063
C0206641 Osteochondromatosis EXT2 2132 exostosin glycosyltransferase 2 Q93063
C0011860 Diabetes Mellitus, Non-Insulin-Dependent EXT2 2132 exostosin glycosyltransferase 2 Q93063
C0027651 Neoplasms EXT2 2132 exostosin glycosyltransferase 2 Q93063
C1442903 Exostoses EXT2 2132 exostosin glycosyltransferase 2 Q93063
C0008479 Chondrosarcoma EXT2 2132 exostosin glycosyltransferase 2 Q93063
C0338451 Frontotemporal dementia EXT2 2132 exostosin glycosyltransferase 2 Q93063
C0027543 Avascular necrosis of bone EXT2 2132 exostosin glycosyltransferase 2 Q93063
C3714756 Intellectual Disability EXT2 2132 exostosin glycosyltransferase 2 Q93063
C0152441 Madelung Deformity EXT2 2132 exostosin glycosyltransferase 2 Q93063
C0221356 Brachycephaly EXT2 2132 exostosin glycosyltransferase 2 Q93063
C0015302 External exotoses EXT2 2132 exostosin glycosyltransferase 2 Q93063
C0013336 Dwarfism EXT2 2132 exostosin glycosyltransferase 2 Q93063
C4317295 Congenital disorder of glycosylation type 1s EXT2 2132 exostosin glycosyltransferase 2 Q93063
C0011847 Diabetes EXT2 2132 exostosin glycosyltransferase 2 Q93063
C3279947 NAIL DISORDER, NONSYNDROMIC CONGENITAL, 9 EXT2 2132 exostosin glycosyltransferase 2 Q93063
C0004364 Autoimmune Diseases EXT2 2132 exostosin glycosyltransferase 2 Q93063
C0027708 Nephroblastoma EXT2 2132 exostosin glycosyltransferase 2 Q93063
C0029408 Degenerative polyarthritis EXT2 2132 exostosin glycosyltransferase 2 Q93063
C0020676 Hypothyroidism EXT2 2132 exostosin glycosyltransferase 2 Q93063
C0745103 Hyperlipoproteinemia Type IIa EXT2 2132 exostosin glycosyltransferase 2 Q93063
C0009806 Constipation EXT2 2132 exostosin glycosyltransferase 2 Q93063
C0020538 Hypertensive disease EXT2 2132 exostosin glycosyltransferase 2 Q93063

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024