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 51 - 75 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0410174 Fukuyama Type Congenital Muscular Dystrophy CRPPA 729920 CDP-L-ribitol pyrophosphorylase A A4D126
C0699743 Congenital muscular dystrophy (disorder) CRPPA 729920 CDP-L-ribitol pyrophosphorylase A A4D126
C0279702 Conventional (Clear Cell) Renal Cell Carcinoma CRPPA 729920 CDP-L-ribitol pyrophosphorylase A A4D126
C0002871 Anemia CRPPA 729920 CDP-L-ribitol pyrophosphorylase A A4D126
C0010964 Dandy-Walker Syndrome CRPPA 729920 CDP-L-ribitol pyrophosphorylase A A4D126
C0575158 Kyphoscoliosis deformity of spine CRPPA 729920 CDP-L-ribitol pyrophosphorylase A A4D126
C0266568 Persistent Hyperplastic Primary Vitreous CRPPA 729920 CDP-L-ribitol pyrophosphorylase A A4D126
C0549423 Obstructive Hydrocephalus CRPPA 729920 CDP-L-ribitol pyrophosphorylase A A4D126
C0036572 Seizures CRPPA 729920 CDP-L-ribitol pyrophosphorylase A A4D126
C2936786 Aqueductal Stenosis CRPPA 729920 CDP-L-ribitol pyrophosphorylase A A4D126
C0086543 Cataract CRPPA 729920 CDP-L-ribitol pyrophosphorylase A A4D126
C0026850 Muscular Dystrophy CRPPA 729920 CDP-L-ribitol pyrophosphorylase A A4D126
C0029124 Optic Atrophy CRPPA 729920 CDP-L-ribitol pyrophosphorylase A A4D126
C1531647 Cerebral ventriculomegaly CRPPA 729920 CDP-L-ribitol pyrophosphorylase A A4D126
C0017601 Glaucoma CRPPA 729920 CDP-L-ribitol pyrophosphorylase A A4D126
C0854723 Retinal Dystrophies CRPPA 729920 CDP-L-ribitol pyrophosphorylase A A4D126
C0035305 Retinal Detachment CRPPA 729920 CDP-L-ribitol pyrophosphorylase A A4D126
C0338502 Hypoplasia of the optic nerve CRPPA 729920 CDP-L-ribitol pyrophosphorylase A A4D126
C0231528 Myalgia CRPPA 729920 CDP-L-ribitol pyrophosphorylase A A4D126
C0520947 Clumsiness - motor delay CRPPA 729920 CDP-L-ribitol pyrophosphorylase A A4D126
C2750786 Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency CRPPA 729920 CDP-L-ribitol pyrophosphorylase A A4D126
C0020255 Hydrocephalus CRPPA 729920 CDP-L-ribitol pyrophosphorylase A A4D126
C0266483 Pachygyria CRPPA 729920 CDP-L-ribitol pyrophosphorylase A A4D126
C0032285 Pneumonia CRPPA 729920 CDP-L-ribitol pyrophosphorylase A A4D126
C1879312 Agyria 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