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 11176 - 11200 of 15957 in total
Disease ID Disease Name ▲ Gene Symbol Gene ID Organism Source
DOID:0060740
  • methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency
  • Aliases:
    • methylmalonic acidemia due to methylmalonyl-CoA mutase deficiency
    • methylmalonic aciduria mut type
    • vitamin B12-unresponsive methylmalonic aciduria
Homo sapiens (human)
DOID:0060740
  • methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency
  • Aliases:
    • methylmalonic acidemia due to methylmalonyl-CoA mutase deficiency
    • methylmalonic aciduria mut type
    • vitamin B12-unresponsive methylmalonic aciduria
Mus musculus (house mouse)
DOID:0050452
  • mevalonic aciduria
  • Aliases:
    • Mevalonate Kinase Deficiency
Rattus norvegicus (Norway rat)
DOID:0050452
  • mevalonic aciduria
  • Aliases:
    • Mevalonate Kinase Deficiency
Homo sapiens (human)
DOID:0050452
  • mevalonic aciduria
  • Aliases:
    • Mevalonate Kinase Deficiency
Mus musculus (house mouse)
DOID:0060609
  • microcephalic osteodysplastic primordial dwarfism type II
  • Aliases:
    • Majewski osteodysplastic primordial dwarfism type II
    • osteodysplastic primordial dwarfism type II
Homo sapiens (human)
DOID:0080105
  • microcephaly and chorioretinopathy 1
Mus musculus (house mouse)
DOID:0080105
  • microcephaly and chorioretinopathy 1
Homo sapiens (human)
DOID:0080107
  • microcephaly and chorioretinopathy 3
Homo sapiens (human)
DOID:0060349
  • microcephaly with or without chorioretinopathy, lymphedema, or mental retardation
  • Aliases:
    • chorioretinal dysplasia-microcephaly-mental retardation syndrome
    • lymphedema and retinal folds with ficrocephaly and microphthalmos
    • lymphedema, microcephaly and chorioretinopathy syndrome
    • microcephaly lymphedema chorioretinal dysplasia
    • microcephaly, lymphedema, chorioretinal dysplasia syndrome
Homo sapiens (human)
DOID:10907
  • microcephaly
  • Aliases:
    • Microcephalus
    • microencephaly
Homo sapiens (human)
DOID:10907
  • microcephaly
  • Aliases:
    • Microcephalus
    • microencephaly
Drosophila melanogaster (fruit fly)
DOID:10907
  • microcephaly
  • Aliases:
    • Microcephalus
    • microencephaly
Xenopus tropicalis (tropical clawed frog)
DOID:10907
  • microcephaly
  • Aliases:
    • Microcephalus
    • microencephaly
Danio rerio (zebrafish)
DOID:10907
  • microcephaly
  • Aliases:
    • Microcephalus
    • microencephaly
Mus musculus (house mouse)
DOID:10907
  • microcephaly
  • Aliases:
    • Microcephalus
    • microencephaly
Rattus norvegicus (Norway rat)
DOID:0081051
  • microcephaly, growth deficiency, seizures, and brain malformations
Mus musculus (house mouse)
DOID:11252
  • microcytic anemia
Rattus norvegicus (Norway rat)
DOID:11252
  • microcytic anemia
Mus musculus (house mouse)
DOID:11252
  • microcytic anemia
Saccharomyces cerevisiae S288C
DOID:11252
  • microcytic anemia
Homo sapiens (human)
DOID:0112234
  • microlissencephaly
Mus musculus (house mouse)
DOID:0112234
  • microlissencephaly
Homo sapiens (human)
DOID:0060861
  • microphthalmia with limb anomalies
  • Aliases:
    • MLA
    • OAS
    • Waardenburg anophthalmia syndrome
    • anophthalmia-syndactyly syndrome
    • ophthalmoacromelic syndrome
Mus musculus (house mouse)
DOID:0060861
  • microphthalmia with limb anomalies
  • Aliases:
    • MLA
    • OAS
    • Waardenburg anophthalmia syndrome
    • anophthalmia-syndactyly syndrome
    • ophthalmoacromelic syndrome
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