GlyCosmos Diseases

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

Source Last Updated
Alliance of Genome Resources July 29, 2024
DisGeNET July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 401 - 425 of 7942 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism
DOID:13375
  • temporal arteritis
  • Aliases:
    • Horton's disease
    • giant cell arteritis
Mus musculus (house mouse)
DOID:6951
  • telangiectatic osteogenic sarcoma
  • Aliases:
    • Telangiectatic osteosarcoma
Homo sapiens (human)
DOID:1272
  • telangiectasis
  • Aliases:
    • telangiectasia
Homo sapiens (human)
DOID:680
  • tauopathy
Homo sapiens (human)
DOID:0050789
  • tarsal-carpal coalition syndrome
Homo sapiens (human)
DOID:5504
  • tanycytic ependymoma
Homo sapiens (human)
DOID:9651
  • systolic heart failure
Homo sapiens (human)
DOID:418
  • systemic scleroderma
  • Aliases:
    • Scleroderma
    • Scleroderma syndrome
    • progressive systemic sclerosis
    • systemic sclerosis
Caenorhabditis elegans
DOID:418
  • systemic scleroderma
  • Aliases:
    • Scleroderma
    • Scleroderma syndrome
    • progressive systemic sclerosis
    • systemic sclerosis
Homo sapiens (human)
DOID:418
  • systemic scleroderma
  • Aliases:
    • Scleroderma
    • Scleroderma syndrome
    • progressive systemic sclerosis
    • systemic sclerosis
Mus musculus (house mouse)
DOID:418
  • systemic scleroderma
  • Aliases:
    • Scleroderma
    • Scleroderma syndrome
    • progressive systemic sclerosis
    • systemic sclerosis
Drosophila melanogaster (fruit fly)
DOID:418
  • systemic scleroderma
  • Aliases:
    • Scleroderma
    • Scleroderma syndrome
    • progressive systemic sclerosis
    • systemic sclerosis
Saccharomyces cerevisiae S288C
DOID:418
  • systemic scleroderma
  • Aliases:
    • Scleroderma
    • Scleroderma syndrome
    • progressive systemic sclerosis
    • systemic sclerosis
Rattus norvegicus (Norway rat)
DOID:14365
  • systemic primary carnitine deficiency disease
  • Aliases:
    • carnitine transporter deficiency
    • carnitine uptake defect
    • deficiency of plasma-membrane carnitine transporter
    • primary carnitine deficiency
    • renal carnitine transport defect
Homo sapiens (human)
DOID:349
  • systemic mastocytosis
  • Aliases:
    • SMCD - systemic mast cell disease
    • systemic tissue mast cell disease
Homo sapiens (human)
DOID:9074
  • systemic lupus erythematosus
  • Aliases:
    • Lupus Erythematosus, systemic
    • SLE - Lupus Erythematosus, systemic
    • disseminated lupus erythematosus
Rattus norvegicus (Norway rat)
DOID:9074
  • systemic lupus erythematosus
  • Aliases:
    • Lupus Erythematosus, systemic
    • SLE - Lupus Erythematosus, systemic
    • disseminated lupus erythematosus
Mus musculus (house mouse)
DOID:9074
  • systemic lupus erythematosus
  • Aliases:
    • Lupus Erythematosus, systemic
    • SLE - Lupus Erythematosus, systemic
    • disseminated lupus erythematosus
Drosophila melanogaster (fruit fly)
DOID:9074
  • systemic lupus erythematosus
  • Aliases:
    • Lupus Erythematosus, systemic
    • SLE - Lupus Erythematosus, systemic
    • disseminated lupus erythematosus
Homo sapiens (human)
DOID:0070324
  • systemic Epstein-Barr virus positive T-cell lymphoma of childhood
  • Aliases:
    • EBV-positive T-cell lymphoproliferative disorder of childhood
    • systemic EBV-positive T-cell lymphoma of childhood
Homo sapiens (human)
DOID:327
  • syringomyelia
Homo sapiens (human)
DOID:2065
  • syringoma
Homo sapiens (human)
DOID:2703
  • synovitis
Homo sapiens (human)
DOID:5485
  • synovial sarcoma
Homo sapiens (human)
DOID:0050888
  • syndromic intellectual disability
Homo sapiens (human)

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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


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Last updated: August 19, 2024