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 6676 - 6700 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism
DOID:9072
  • lethal midline granuloma
  • Aliases:
    • Midfacial Necrotising Lesion
    • malignant granuloma of face
Homo sapiens (human)
DOID:11206
  • opioid abuse
Homo sapiens (human)
DOID:1523
  • colon lymphoma
  • Aliases:
    • Colonic Lymphoma
Homo sapiens (human)
DOID:4769
  • pleuropulmonary blastoma
Homo sapiens (human)
DOID:8162
  • thyroid Hurthle cell adenoma
  • Aliases:
    • benign oncocytoma of the thyroid
Homo sapiens (human)
DOID:9254
  • mast-cell leukemia
Homo sapiens (human)
DOID:698
  • dentin sensitivity
  • Aliases:
    • Sensitive dentin
Homo sapiens (human)
DOID:14089
  • root caries
  • Aliases:
    • Cementum caries
    • Dental caries of root surface
Homo sapiens (human)
DOID:0080488
  • mucolipidosis
Homo sapiens (human)
DOID:0070384
  • developmental and epileptic encephalopathy 98
  • Aliases:
    • DEE98
    • early infantile epileptic encephalopathy 98
Homo sapiens (human)
DOID:0060350
  • adenine phosphoribosyltransferase deficiency
  • Aliases:
    • 2,8-dihydroxyadenine urolithiasis
    • APRT deficiency
Drosophila melanogaster (fruit fly)
DOID:0111260
  • phosphoribosylpyrophosphate synthetase superactivity
  • Aliases:
    • PRPP synthetase superactivity
    • PRPS1 superactivity
Homo sapiens (human)
DOID:613
  • obsolete T lymphocyte deficiency
Homo sapiens (human)
DOID:11200
  • T cell deficiency
  • Aliases:
    • T cell immunodeficiency
    • T lymphocyte deficiency
    • T lymphocyte immunodeficiency
Homo sapiens (human)
DOID:2012
  • Nezelof syndrome
  • Aliases:
    • Nezelof's syndrome
    • T-cell immunodeficiency with thymic aplasia
    • TIDTA
    • thymic aplasia
    • thymic dysplasia with normal immunoglobulins
Homo sapiens (human)
DOID:5813
  • purine nucleoside phosphorylase deficiency
  • Aliases:
    • PNP deficiency
    • Purine-Nucleoside Phosphorylase deficiency
    • deficiency of inosine phosphorylase
Homo sapiens (human)
DOID:0060010
  • Omenn syndrome
  • Aliases:
    • combined immunodeficiency with hypereosinophilia
Homo sapiens (human)
DOID:525
  • central nervous system vasculitis
Homo sapiens (human)
DOID:2555
  • granulomatous angiitis
Homo sapiens (human)
DOID:2562
  • suppurative periapical periodontitis
  • Aliases:
    • Apical abscess
    • Dentoalveolar abscess
    • Periapical abscess
    • Suppurative apical periodontitis
Homo sapiens (human)
DOID:0050644
  • arterial calcification of infancy
  • Aliases:
    • generalized arterial calcification of infancy
    • idiopathic infantile arterial calcification
    • infantile arteriosclerosis
Homo sapiens (human)
DOID:0050854
  • Muckle-Wells syndrome
  • Aliases:
    • MWS
    • neutrophilic urticaria
Homo sapiens (human)
DOID:0060322
  • mastoiditis
Homo sapiens (human)
DOID:0050645
  • arterial tortuosity syndrome
Homo sapiens (human)
DOID:4734
  • calciphylaxis
Homo sapiens (human)

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Last updated: August 19, 2024