GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources July 29, 2024
DisGeNET July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 301 - 325 of 7942 in total
Disease ID Disease Name ▲ Gene Symbol Gene ID Organism
DOID:11725
  • Cornelia de Lange syndrome
  • Aliases:
    • Brachmann de Lange syndrome
    • De Lange syndrome
Homo sapiens (human)
DOID:11725
  • Cornelia de Lange syndrome
  • Aliases:
    • Brachmann de Lange syndrome
    • De Lange syndrome
Saccharomyces cerevisiae S288C
DOID:11725
  • Cornelia de Lange syndrome
  • Aliases:
    • Brachmann de Lange syndrome
    • De Lange syndrome
Drosophila melanogaster (fruit fly)
DOID:0080599
  • Coronavirus infectious disease
Homo sapiens (human)
DOID:0050469
  • Costello syndrome
  • Aliases:
    • FCS SYNDROME
    • Faciocutaneoskeletal Syndrome
Homo sapiens (human)
DOID:0081001
  • Cowden syndrome 5
Homo sapiens (human)
DOID:0081001
  • Cowden syndrome 5
Mus musculus (house mouse)
DOID:0081001
  • Cowden syndrome 5
Rattus norvegicus (Norway rat)
DOID:0081002
  • Cowden syndrome 6
Mus musculus (house mouse)
DOID:0081002
  • Cowden syndrome 6
Homo sapiens (human)
DOID:0081002
  • Cowden syndrome 6
Rattus norvegicus (Norway rat)
DOID:0081002
  • Cowden syndrome 6
Xenopus laevis (African clawed frog)
DOID:6457
  • Cowden syndrome
  • Aliases:
    • Cowden disease
    • Lhermitte-Duclos disease
    • dysplastic Gangliocytoma of Cerebellum
Homo sapiens (human)
DOID:11949
  • Creutzfeldt-Jakob disease
  • Aliases:
    • CJD
    • Creutzfeldt Jacob syndrome
    • Creutzfeldt Jakob disease
    • Creutzfeldt-Jacob disease
    • Jakob-Creutzfeldt disease
    • Subacute spongiform encephalopathy
    • Transmissible virus dementia
Homo sapiens (human)
DOID:11949
  • Creutzfeldt-Jakob disease
  • Aliases:
    • CJD
    • Creutzfeldt Jacob syndrome
    • Creutzfeldt Jakob disease
    • Creutzfeldt-Jacob disease
    • Jakob-Creutzfeldt disease
    • Subacute spongiform encephalopathy
    • Transmissible virus dementia
Caenorhabditis elegans
DOID:11949
  • Creutzfeldt-Jakob disease
  • Aliases:
    • CJD
    • Creutzfeldt Jacob syndrome
    • Creutzfeldt Jakob disease
    • Creutzfeldt-Jacob disease
    • Jakob-Creutzfeldt disease
    • Subacute spongiform encephalopathy
    • Transmissible virus dementia
Xenopus tropicalis (tropical clawed frog)
DOID:11949
  • Creutzfeldt-Jakob disease
  • Aliases:
    • CJD
    • Creutzfeldt Jacob syndrome
    • Creutzfeldt Jakob disease
    • Creutzfeldt-Jacob disease
    • Jakob-Creutzfeldt disease
    • Subacute spongiform encephalopathy
    • Transmissible virus dementia
Danio rerio (zebrafish)
DOID:11949
  • Creutzfeldt-Jakob disease
  • Aliases:
    • CJD
    • Creutzfeldt Jacob syndrome
    • Creutzfeldt Jakob disease
    • Creutzfeldt-Jacob disease
    • Jakob-Creutzfeldt disease
    • Subacute spongiform encephalopathy
    • Transmissible virus dementia
Mus musculus (house mouse)
DOID:11949
  • Creutzfeldt-Jakob disease
  • Aliases:
    • CJD
    • Creutzfeldt Jacob syndrome
    • Creutzfeldt Jakob disease
    • Creutzfeldt-Jacob disease
    • Jakob-Creutzfeldt disease
    • Subacute spongiform encephalopathy
    • Transmissible virus dementia
Xenopus laevis (African clawed frog)
DOID:12580
  • Cri-Du-Chat syndrome
  • Aliases:
    • 5p deletion syndrome
    • 5p partial monosomy syndrome
    • chromosome 5 short arm deletion syndrome
    • chromosome 5p deletion syndrome
Homo sapiens (human)
DOID:3803
  • Crigler-Najjar syndrome
  • Aliases:
    • Bilirubin UDP glucuronyl transferase deficiency
    • Crigler Najjar syndrome
    • Crigler-Najjar syndrome, type I
Danio rerio (zebrafish)
DOID:3803
  • Crigler-Najjar syndrome
  • Aliases:
    • Bilirubin UDP glucuronyl transferase deficiency
    • Crigler Najjar syndrome
    • Crigler-Najjar syndrome, type I
Xenopus tropicalis (tropical clawed frog)
DOID:3803
  • Crigler-Najjar syndrome
  • Aliases:
    • Bilirubin UDP glucuronyl transferase deficiency
    • Crigler Najjar syndrome
    • Crigler-Najjar syndrome, type I
Homo sapiens (human)
DOID:3803
  • Crigler-Najjar syndrome
  • Aliases:
    • Bilirubin UDP glucuronyl transferase deficiency
    • Crigler Najjar syndrome
    • Crigler-Najjar syndrome, type I
Rattus norvegicus (Norway rat)
DOID:3803
  • Crigler-Najjar syndrome
  • Aliases:
    • Bilirubin UDP glucuronyl transferase deficiency
    • Crigler Najjar syndrome
    • Crigler-Najjar syndrome, type I
Drosophila melanogaster (fruit fly)

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