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 7951 - 7975 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:1532
  • pleural disease
  • Aliases:
    • disorder of pleura
    • non-neoplastic pleural disease
Homo sapiens (human)
DOID:0060108
  • brain glioma
  • Aliases:
    • lower grade glioma
Mus musculus (house mouse)
DOID:11720
  • distal myopathy
  • Aliases:
    • distal muscular dystrophy
Homo sapiens (human)
DOID:0110212
  • Charcot-Marie-Tooth disease X-linked recessive 4
  • Aliases:
    • CMT4X
    • CMTX4
    • Charcot-Marie-Tooth disease with deafness and mental retardation
    • Cowchock syndrome
    • NADMR
    • NAMSD
    • X-linked Charcot-Marie-Tooth disease type 4
    • axonal motor sensory neuropathy with deafness and mental retardation
Homo sapiens (human)
DOID:13208
  • background diabetic retinopathy
  • Aliases:
    • Non proliferative diabetic retinopathy
    • Non-Proliferative Diabetic Retinopathy
Homo sapiens (human)
DOID:423
  • myopathy
Homo sapiens (human)
DOID:13254
  • diverticulitis of colon
  • Aliases:
    • colonic diverticular disease
Mus musculus (house mouse)
DOID:1380
  • endometrial cancer
  • Aliases:
    • endometrial Ca
    • endometrial neoplasm
    • malignant endometrial neoplasm
    • malignant neoplasm of endometrium
    • neoplasm of endometrium
    • primary malignant neoplasm of endometrium
    • tumor of Endometrium
Caenorhabditis elegans
DOID:0111840
  • Van Esch-O'Driscoll syndrome
  • Aliases:
    • MRXSVEOD
    • VEODS
    • X-linked intellectual disability, Van Esch type
    • X-linked syndromic mental retardation Van Esch-O'Driscoll type
Saccharomyces cerevisiae S288C
DOID:0050704
  • childhood electroclinical syndrome
Danio rerio (zebrafish)
DOID:0110279
  • autosomal recessive limb-girdle muscular dystrophy type 2E
  • Aliases:
    • Beta-sarcoglycanopathy
    • LGMD2E
    • Limb-girdle muscular dystrophy due to beta-sarcoglycan deficiency
    • muscular dystrophy, limb-girdle, type 2E
Mus musculus (house mouse)
DOID:10457
  • Legionnaires' disease
  • Aliases:
    • Infection by Legionella pneumophilia
    • Legionella
    • Legionella pneumonia
    • Legionnaire's disease
Drosophila melanogaster (fruit fly)
DOID:0110289
  • autosomal recessive limb-girdle muscular dystrophy type 2Y
  • Aliases:
    • LGMD2Y
    • autosomal recessive muscular dystrophy due to LAP1B deficiency
    • autosomal recessive muscular dystrophy due to Torsin-1A-interacting protein 1 deficiency
    • muscular dystrophy with progressive weakness, distal contractures and rigid spine
    • muscular dystrophy, limb-girdle, type 2Y
Mus musculus (house mouse)
DOID:0060685
  • autosomal dominant nocturnal frontal lobe epilepsy 4
  • Aliases:
    • ENFL4
    • nocturnal frontal lobe epilepsy 4
Drosophila melanogaster (fruit fly)
DOID:13139
  • crescentic glomerulonephritis
Rattus norvegicus (Norway rat)
DOID:9822
  • partial central choroid dystrophy
  • Aliases:
    • Choroidal dystrophy, central areolar
Mus musculus (house mouse)
DOID:14330
  • Parkinson's disease
  • Aliases:
    • Parkinson disease
    • paralysis agitans
Saccharomyces cerevisiae S288C
DOID:0110372
  • retinitis pigmentosa 4
  • Aliases:
    • RP4
Xenopus laevis (African clawed frog)
DOID:12466
  • secondary hyperparathyroidism
Homo sapiens (human)
DOID:0110957
  • Gaucher's disease type I
  • Aliases:
    • Acid Beta-Glucosidase Deficiency
    • GD I
    • GD1
    • Gaucher Disease, Noncerebral Juvenile
    • Gba Deficiency
    • Glucocerebrosidase Deficiency
Homo sapiens (human)
DOID:0111432
  • essential tremor 5
  • Aliases:
    • ETM5
    • hereditary essential tremor 5
Caenorhabditis elegans
DOID:0110661
  • congenital myasthenic syndrome 20
  • Aliases:
    • CMS20
    • congenital myasthenic syndrome 20 presynaptic
Homo sapiens (human)
DOID:0111700
  • ankyrin-B-related cardiac arrhythmia
  • Aliases:
    • ankyrin-B syndrome
Homo sapiens (human)
DOID:0060257
  • dyschromatosis symmetrica hereditaria
  • Aliases:
    • reticulate acropigmentation of Dohi
Mus musculus (house mouse)
DOID:0060703
  • Muenke Syndrome
  • Aliases:
    • FGFR3-related craniosynostosis
Xenopus laevis (African clawed frog)
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