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 11326 - 11350 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼ Source
DOID:0080567
  • congenital disorder of glycosylation Ip
  • Aliases:
    • congenital disorder of glycosylation 1p
Homo sapiens (human)
DOID:0111834
  • X-linked reticulate pigmentary disorder
  • Aliases:
    • Partington disease
    • X-linked reticulate pigmentary disorder with systemic manifestations
Homo sapiens (human)
DOID:0111870
  • nonphotosensitive trichothiodystrophy 7
  • Aliases:
    • TTD7
Homo sapiens (human)
DOID:0060209
  • amyotrophic lateral sclerosis type 18
  • Aliases:
    • ALS18
    • amyotrophic lateral sclerosis 18
Homo sapiens (human)
DOID:0080471
  • developmental and epileptic encephalopathy 92
Homo sapiens (human)
DOID:14184
  • polyneuropathy due to drug
Homo sapiens (human)
DOID:7442
  • monoclonal gammopathy of uncertain significance
  • Aliases:
    • MGUS
    • Monoclonal gammopathy of undetermined significance
Homo sapiens (human)
DOID:0080212
  • polycystic kidney disease 4
Homo sapiens (human)
DOID:0080242
  • syndromic X-linked mental retardation Hough type
Homo sapiens (human)
DOID:14221
  • abdominal obesity-metabolic syndrome 1
  • Aliases:
    • dysmetabolic syndrome X
    • metabolic syndrome X
Homo sapiens (human)
DOID:0110350
  • osteogenesis imperfecta type 6
  • Aliases:
    • OI6
    • osteogenesis imperfecta type VI
Homo sapiens (human)
DOID:0112193
  • tetraamelia syndrome 2
  • Aliases:
    • TETAMS2
    • tetra-amelia with pulmonary hypoplasia
    • tetraamelia with pulmonary hypoplasia
Homo sapiens (human)
DOID:0070182
  • spermatogenic failure 13
  • Aliases:
    • SPGF13
Homo sapiens (human)
DOID:0050657
  • Bannayan-Riley-Ruvalcaba syndrome
  • Aliases:
    • Bannayan-Zonana syndrome
    • Cowden syndrome 1
    • Riley-Smith syndrome
    • Ruvalcaba-Myhre-Smith syndrome
Homo sapiens (human)
DOID:0050338
  • primary bacterial infectious disease
Homo sapiens (human)
DOID:422
  • congenital structural myopathy
Homo sapiens (human)
DOID:0112029
  • non-syndromic X-linked intellectual disability 50
  • Aliases:
    • MRX50
    • X-linked intellectual developmental disorder 50
    • X-linked mental retardation 50
    • XLID50
Homo sapiens (human)
DOID:0080038
  • pycnodysostosis
Homo sapiens (human)
DOID:8805
  • intermediate coronary syndrome
  • Aliases:
    • Angina at rest
    • Anginal chest pain at rest
    • Impending infarction
    • Preinfarction angina
    • Unstable angina
    • Worsening angina
Homo sapiens (human)
DOID:14775
  • brittle cornea syndrome 1
  • Aliases:
    • type VIB Ehlers-Danlos syndrome
Homo sapiens (human)
DOID:0050954
  • spinocerebellar ataxia type 1
Homo sapiens (human)
DOID:0111398
  • congenital dyserythropoietic anemia type Ia
  • Aliases:
    • CDA Ia
    • CDAN1A
Homo sapiens (human)
DOID:0111959
  • immunodeficiency 15B
  • Aliases:
    • IMD15B
Homo sapiens (human)
DOID:10579
  • leukodystrophy
Homo sapiens (human)
DOID:2383
  • neonatal jaundice
  • Aliases:
    • neonatal hyperbilirubinemia
    • neonatal icterus
Homo sapiens (human)
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