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 5326 - 5350 of 15957 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism Source
DOID:0050869
  • villous adenoma
Mus musculus (house mouse)
DOID:0070397
  • hypomyelinating leukodystrophy 23
  • Aliases:
    • HLD23
Mus musculus (house mouse)
DOID:0112209
  • developmental and epileptic encephalopathy 73
  • Aliases:
    • DEE73
    • early infantile epileptic encephalopathy 73
Rattus norvegicus (Norway rat)
DOID:0112209
  • developmental and epileptic encephalopathy 73
  • Aliases:
    • DEE73
    • early infantile epileptic encephalopathy 73
Mus musculus (house mouse)
DOID:0081007
  • RNASET2-deficient cystic leukoencephalopathy
  • Aliases:
    • cystic leukoencephalopathy without megalencephaly
    • infantile-onset RNASET2 deficient cystic leukoencephalopathy
Mus musculus (house mouse)
DOID:5410
  • pulmonary neuroendocrine tumor
Mus musculus (house mouse)
DOID:0110862
  • congenital stationary night blindness autosomal dominant 1
  • Aliases:
    • CSNBAD1
    • rhodopsin-related congenital stationary night blindness
Rattus norvegicus (Norway rat)
DOID:8499
  • night blindness
  • Aliases:
    • nyctalopia
Rattus norvegicus (Norway rat)
DOID:0110862
  • congenital stationary night blindness autosomal dominant 1
  • Aliases:
    • CSNBAD1
    • rhodopsin-related congenital stationary night blindness
Mus musculus (house mouse)
DOID:4175
  • Rh isoimmunization
  • Aliases:
    • Rh incompatibility affecting management of mother
Mus musculus (house mouse)
DOID:0111506
  • palmoplantar keratoderma-esophageal carcinoma syndrome
  • Aliases:
    • Bennion-Patterson syndrome
    • Howell-Evans syndrome
    • TOC
    • keratosis palmaris et plantaris with esophageal cancer
    • keratosis palmoplantaris-esophageal carcinoma syndrome
    • palmoplantar hyperkeratosis-esophageal carcinoma syndrome
    • palmoplantar keratoderma with esophageal cancer
    • tylosis with esophageal cancer
    • tylosis-oesophageal carcinoma syndrome
Mus musculus (house mouse)
DOID:0111562
  • overhydrated hereditary stomatocytosis
  • Aliases:
    • OHS
    • potassium sodium disorder of erythrocyte
    • stomatocytosisIOHST
Rattus norvegicus (Norway rat)
DOID:0050641
  • Rh deficiency syndrome
Rattus norvegicus (Norway rat)
DOID:0111562
  • overhydrated hereditary stomatocytosis
  • Aliases:
    • OHS
    • potassium sodium disorder of erythrocyte
    • stomatocytosisIOHST
Mus musculus (house mouse)
DOID:0050641
  • Rh deficiency syndrome
Mus musculus (house mouse)
DOID:0050430
  • multiple endocrine neoplasia type 2A
  • Aliases:
    • MEN2A
    • Sipple syndrome
    • multiple endocrine neoplasia II
Rattus norvegicus (Norway rat)
DOID:0080204
  • renal hypoplasia
Rattus norvegicus (Norway rat)
DOID:10016
  • multiple endocrine neoplasia type 2B
  • Aliases:
    • MEN type IIB
    • MEN2B
    • Multiple endocrine neoplasia, type 3
    • Wagenmann-Froboese syndrome
    • mucosal neuroma syndrome
Rattus norvegicus (Norway rat)
DOID:10016
  • multiple endocrine neoplasia type 2B
  • Aliases:
    • MEN type IIB
    • MEN2B
    • Multiple endocrine neoplasia, type 3
    • Wagenmann-Froboese syndrome
    • mucosal neuroma syndrome
Mus musculus (house mouse)
DOID:0080204
  • renal hypoplasia
Mus musculus (house mouse)
DOID:0050430
  • multiple endocrine neoplasia type 2A
  • Aliases:
    • MEN2A
    • Sipple syndrome
    • multiple endocrine neoplasia II
Mus musculus (house mouse)
DOID:0080280
  • gingival fibromatosis 5
Mus musculus (house mouse)
DOID:0110556
  • autosomal dominant nonsyndromic deafness 27
  • Aliases:
    • DFNA27
    • autosomal dominant deafness 27
Mus musculus (house mouse)
DOID:0080827
  • human cytomegalovirus infection
Mus musculus (house mouse)
DOID:0050811
  • congenital adrenal hyperplasia
  • Aliases:
    • adrenal hyperplasia 1
    • congenital lipoid adrenal hyperplasia
    • lipoid CAH
Rattus norvegicus (Norway rat)
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