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 801 - 825 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism
DOID:0050784
  • primary progressive multiple sclerosis
  • Aliases:
    • PPMS
    • Primary-progressive MS
Homo sapiens (human)
DOID:467
  • venous hemangioma
Homo sapiens (human)
DOID:4400
  • dermatosis papulosa nigra
Homo sapiens (human)
DOID:4151
  • skull base chordoma
  • Aliases:
    • Chordoma of the Skull Base
Homo sapiens (human)
DOID:0050256
  • angiostrongyliasis
Homo sapiens (human)
DOID:0111120
  • nephronophthisis 9
  • Aliases:
    • NPHP9
Homo sapiens (human)
DOID:11563
  • retinal vasculitis
Homo sapiens (human)
DOID:3277
  • thymus cancer
  • Aliases:
    • Thymic tumor
    • neoplasm of thymus
    • thymic neoplasm
Homo sapiens (human)
DOID:1687
  • neovascular glaucoma
  • Aliases:
    • secondary angle-closure glaucoma with rubeosis
Homo sapiens (human)
DOID:1759
  • American histoplasmosis
Homo sapiens (human)
DOID:0112361
  • spondylocostal dysostosis 3
  • Aliases:
    • SCDO3
    • autosomal recessive spondylocostal dysostosis 3
Homo sapiens (human)
DOID:0111334
  • congenital leptin deficiency
  • Aliases:
    • LEPD
    • leptin deficiency or dysfunction
    • obesity due to congenital leptin deficiency
Homo sapiens (human)
DOID:10605
  • short bowel syndrome
  • Aliases:
    • acquired short bowel syndrome
    • short gut syndrome
Homo sapiens (human)
DOID:5139
  • cellular leiomyoma
Homo sapiens (human)
DOID:8503
  • impetigo herpetiformis
Homo sapiens (human)
DOID:3611
  • acute retinal necrosis syndrome
  • Aliases:
    • acute retinal necrosis
Homo sapiens (human)
DOID:0111646
  • congenital lactase deficiency
  • Aliases:
    • CLD
    • congenital alactasia
    • congenital alactasia syndrome
    • congenital lactose intolerance
    • congenital lactose malabsorption
    • disaccharide intolerance II
Homo sapiens (human)
DOID:1134
  • gingival recession
  • Aliases:
    • Gingival recession, localized
    • localized gingival recession
    • minimal gingival recession
    • moderate gingival recession
    • severe gingival recession
Homo sapiens (human)
DOID:12318
  • granular corneal dystrophy
Homo sapiens (human)
DOID:4376
  • milk allergy
  • Aliases:
    • milk allergic reaction
Homo sapiens (human)
DOID:5884
  • benign intermediate mesothelioma
  • Aliases:
    • Well-differentiated Papillary tumor of Mesothelium
Homo sapiens (human)
DOID:8568
  • infectious mononucleosis
  • Aliases:
    • Filatov's disease
    • Gammaherpesviral mononucleosis
    • Monocytic angina
    • Pfeiffer's disease
    • glandular fever
    • mononucleosis
Homo sapiens (human)
DOID:0090142
  • cystathioninuria
  • Aliases:
    • cystathionase deficiency
    • cystathione gamma-lyase deficiency syndrome
    • gamma-cystathionase deficiency
Homo sapiens (human)
DOID:2978
  • carbohydrate metabolic disorder
  • Aliases:
    • disorder of carbohydrate transport and metabolism
    • inborn carbohydrate metabolism disorder
    • inborn errors of carbohydrate metabolism
Homo sapiens (human)
DOID:0111680
  • essential fructosuria
  • Aliases:
    • fructokinase deficiency
    • hepatic fructokinase deficiency
    • ketohexokinase deficiency
Homo sapiens (human)

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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