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 58526 - 58550 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
C0030319 Panic Disorder CDS1 1040 CDP-diacylglycerol synthase 1 Q92903
C0010232 Cowpox CDS1 1040 CDP-diacylglycerol synthase 1 Q92903
C1621958 Glioblastoma Multiforme CDS1 1040 CDP-diacylglycerol synthase 1 Q92903
C0039483 Giant Cell Arteritis CDS1 1040 CDP-diacylglycerol synthase 1 Q92903
C0013146 Drug abuse CDS1 1040 CDP-diacylglycerol synthase 1 Q92903
C0079731 B-Cell Lymphomas CDS1 1040 CDP-diacylglycerol synthase 1 Q92903
C0018801 Heart failure CDS1 1040 CDP-diacylglycerol synthase 1 Q92903
C0025289 Meningitis CDS1 1040 CDP-diacylglycerol synthase 1 Q92903
C0006142 Malignant neoplasm of breast CDS1 1040 CDP-diacylglycerol synthase 1 Q92903
C0008479 Chondrosarcoma CDS1 1040 CDP-diacylglycerol synthase 1 Q92903
C0278878 Adult Glioblastoma CDS1 1040 CDP-diacylglycerol synthase 1 Q92903
C0026896 Myasthenia Gravis CDS1 1040 CDP-diacylglycerol synthase 1 Q92903
C0340569 Internal Carotid Artery Stenosis CDS1 1040 CDP-diacylglycerol synthase 1 Q92903
C0006826 Malignant Neoplasms CDS1 1040 CDP-diacylglycerol synthase 1 Q92903
C0009451 Communicating Hydrocephalus CRPPA 729920 CDP-L-ribitol pyrophosphorylase A A4D126
C0686353 Muscular Dystrophies, Limb-Girdle CRPPA 729920 CDP-L-ribitol pyrophosphorylase A A4D126
C3553330 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7 CRPPA 729920 CDP-L-ribitol pyrophosphorylase A A4D126
C0026848 Myopathy CRPPA 729920 CDP-L-ribitol pyrophosphorylase A A4D126
C4015095 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7 CRPPA 729920 CDP-L-ribitol pyrophosphorylase A A4D126
C0010038 Corneal Opacity CRPPA 729920 CDP-L-ribitol pyrophosphorylase A A4D126
C0266544 Microcornea CRPPA 729920 CDP-L-ribitol pyrophosphorylase A A4D126
C0020256 Congenital Hydrocephalus CRPPA 729920 CDP-L-ribitol pyrophosphorylase A A4D126
C0265221 Walker-Warburg congenital muscular dystrophy CRPPA 729920 CDP-L-ribitol pyrophosphorylase A A4D126
C4284790 Muscular Dystrophy-Dystroglycanopathy (Congenital with Brain and Eye Anomalies) Type A, 1 CRPPA 729920 CDP-L-ribitol pyrophosphorylase A A4D126
C0015393 Eye Abnormalities CRPPA 729920 CDP-L-ribitol pyrophosphorylase A A4D126

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