Table Filtering
Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
Resources Genes Glycoproteins Lectins Glycolipids Glycans Pathways Diseases Organisms
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Other Information
Release Statistics Download
Tools
SugarDrawer GlycanBuilder Glycan Converters GlycoMaple GlycomeAtlas LM-GlycomeAtlas GALAXY MCAW GlycoSim GRable
Search Tools
Cross Search Glycan Search Publication Search Programmatic Access
Standards Ontologies Notations
GlyCosmos Diseases

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

Source Last Updated
Alliance of Genome Resources October 9, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 9226 - 9250 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism Source
DOID:0112158
  • De Sanctis-Cacchione syndrome
  • Aliases:
    • xeroderma pigmentosum with neurologic manifestation
Homo sapiens (human)
DOID:14184
  • polyneuropathy due to drug
Homo sapiens (human)
DOID:0060240
  • UV-sensitive syndrome
Homo sapiens (human)
DOID:0110028
  • age related macular degeneration 5
  • Aliases:
    • ARMD5
Homo sapiens (human)
DOID:0110916
  • hereditary spherocytosis type 1
  • Aliases:
    • HS1
    • SPH1
    • hereditary spherocytosis 1
Mus musculus (house mouse)
DOID:0110918
  • hereditary spherocytosis type 3
  • Aliases:
    • HS3
    • SPH3
    • hereditary spherocytosis 3
Mus musculus (house mouse)
DOID:0060781
  • congenital secretory sodium diarrhea 3
  • Aliases:
    • congenital secretory sodium diarrhea 3 syndromic
    • congenital secretory sodium diarrhea 3 with or without other congenital anomalies
    • congenital secretory sodium diarrhoea 3
    • congenital secretory sodium diarrhoea 3 syndromic
    • congenital secretory sodium diarrhoea 3 with or without other congenital anomalies
Mus musculus (house mouse)
DOID:0110849
  • xeroderma pigmentosum group G
  • Aliases:
    • XP group G
    • XP7
    • XPG
    • xeroderma pigmentosum VII
Homo sapiens (human)
DOID:0080913
  • cerebrooculofacioskeletal syndrome 3
Homo sapiens (human)
DOID:0050117
  • disease by infectious agent
  • Aliases:
    • infectious disease
Homo sapiens (human)
DOID:2962
  • Cockayne syndrome
  • Aliases:
    • Neill-Dingwall syndrome
Homo sapiens (human)
DOID:2596
  • larynx cancer
Homo sapiens (human)
DOID:0050831
  • familial encephalopathy with neuroserpin inclusion bodies
  • Aliases:
    • FENIB
Mus musculus (house mouse)
DOID:0060186
  • chemical colitis
Mus musculus (house mouse)
DOID:13372
  • alpha 1-antitrypsin deficiency
  • Aliases:
    • AAT deficiency
Mus musculus (house mouse)
DOID:0110440
  • dilated cardiomyopathy 1J
  • Aliases:
    • CMD1J
    • autosomal dominant dilated cardiomyopathy with sensorineural hearing loss
    • neurosensory deafness with dilated cardiomyopathy
    • neurosensory hearing loss with dilated cardiomyopathy
    • sensorineural deafness with dilated cardiomyopathy
    • sensorineural hearing loss with dilated cardiomyopathy
Homo sapiens (human)
DOID:0110542
  • autosomal dominant nonsyndromic deafness 10
  • Aliases:
    • DFNA10
    • autosomal dominant deafness 10
Homo sapiens (human)
DOID:0081002
  • Cowden syndrome 6
Homo sapiens (human)
DOID:13482
  • Proteus syndrome
  • Aliases:
    • Wiedemann's syndrome
Homo sapiens (human)
DOID:607
  • paraplegia
  • Aliases:
    • Paraplegia, lower
Homo sapiens (human)
DOID:1245
  • vulva cancer
  • Aliases:
    • Ca vulva
    • Vulvar tumor
    • malignant Vulvar tumor
    • malignant neoplasm of vulva
    • malignant tumor of vulva
    • neoplasm of vulva
    • vulval cancer
    • vulval neoplasm
    • vulvar neoplasm
Homo sapiens (human)
DOID:7575
  • pancreatic intraductal papillary-mucinous neoplasm
Homo sapiens (human)
DOID:0110338
  • osteogenesis imperfecta type 17
  • Aliases:
    • OI17
    • osteogenesis imperfecta type XVII
Mus musculus (house mouse)
DOID:869
  • cholesteatoma
Homo sapiens (human)
DOID:0111801
  • syndromic microphthalmia 3
  • Aliases:
    • AEG syndrome
    • MCOPS3
    • SOX2 anophthalmia syndrome
    • anophthalmia clinical with associated anomalies
    • anophthalmia esophageal genital syndrome
    • anophthalmia microphthalmia esophageal atresia
    • anophthalmia/microphthalmia-esophageal atresia syndrome
    • microphthalmia and esophageal atresia syndrome
    • syndromic microphthalmia type 3
Mus musculus (house mouse)
Download data in CSV format Download data in TSV format Download data in JSON format
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 v4.1.0

Last updated: December 9, 2024