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 2401 - 2425 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼
DOID:1788
  • peritoneal mesothelioma
  • Aliases:
    • Advanced malignant Mesothelioma of Peritoneum
    • advanced malignant peritoneal mesothelioma
    • malignant mesothelioma of peritoneum
Homo sapiens (human)
DOID:11981
  • morbid obesity
  • Aliases:
    • Severe obesity
Homo sapiens (human)
DOID:4588
  • secretory meningioma
Homo sapiens (human)
DOID:12143
  • neurogenic bladder
  • Aliases:
    • Neuropathic bladder
    • neurogenic dysfunction of the urinary bladder
    • neurogenic urinary bladder disorder
Homo sapiens (human)
DOID:0080563
  • congenital disorder of glycosylation Ik
  • Aliases:
    • congenital disorder of glycosylation 1k
Homo sapiens (human)
DOID:379
  • external ear disease
  • Aliases:
    • Preauricular cyst
    • Preauricular sinus and fistula
    • Preauricular sinus or fistula
Homo sapiens (human)
DOID:2280
  • hidradenitis suppurativa
  • Aliases:
    • Acne inversa, familial
Homo sapiens (human)
DOID:4202
  • brain stem glioma
  • Aliases:
    • Brainstem Neuroglial tumor
Homo sapiens (human)
DOID:4682
  • extrahepatic bile duct carcinoma
  • Aliases:
    • carcinoma of extrahepatic bile duct
    • extrahepatic bile duct cancer
Homo sapiens (human)
DOID:10457
  • Legionnaires' disease
  • Aliases:
    • Infection by Legionella pneumophilia
    • Legionella
    • Legionella pneumonia
    • Legionnaire's disease
Homo sapiens (human)
DOID:12337
  • varicocele
  • Aliases:
    • Scrotal varices
Homo sapiens (human)
DOID:0050534
  • congenital stationary night blindness
  • Aliases:
    • congenital essential nyctalopia
Homo sapiens (human)
DOID:2231
  • factor XII deficiency
  • Aliases:
    • Factor XII deficiency disease
    • Hageman Factor deficiency
    • deficiency, Hageman
Homo sapiens (human)
DOID:0110273
  • autosomal dominant limb-girdle muscular dystrophy
Homo sapiens (human)
DOID:0090142
  • cystathioninuria
  • Aliases:
    • cystathionase deficiency
    • cystathione gamma-lyase deficiency syndrome
    • gamma-cystathionase deficiency
Homo sapiens (human)
DOID:0111256
  • hyperferritinemia-cataract syndrome
  • Aliases:
    • Bonneau-Beaumont syndrome
    • HHCS
    • HRFTC
    • cataract-hyperferritinemia syndrome
    • hereditary hyperferritinemia with congenital cataracts
    • hereditary hyperferritinemia-cataract syndrome
    • hyperferritinemia with or without cataract
Homo sapiens (human)
DOID:13677
  • SAPHO syndrome
  • Aliases:
    • Synovitis, acne, pustulosis palmaris, hyperostosis, osteomyelitis syndrome
Homo sapiens (human)
DOID:0060061
  • primary cutaneous T-cell non-Hodgkin lymphoma
  • Aliases:
    • cutaneous T cell lymphoma
    • cutaneous T-cell lymphoma
Homo sapiens (human)
DOID:3904
  • bronchus carcinoma
  • Aliases:
    • BC - Bronchogenic carcinoma
Homo sapiens (human)
DOID:14753
  • isovaleric acidemia
  • Aliases:
    • Isovaleryl-CoA dehydrogenase deficiency
    • isovaleric acid CoA dehydrogenase deficiency
    • isovaleric aciduria
Homo sapiens (human)
DOID:13789
  • staphyloma posticum
Homo sapiens (human)
DOID:4407
  • phototoxic dermatitis
  • Aliases:
    • Photosensitisation reaction
    • Photosensitive Dermatitis
    • Photosensitiveness
Homo sapiens (human)
DOID:3910
  • lung adenocarcinoma
  • Aliases:
    • bronchogenic lung adenocarcinoma
    • nonsmall cell adenocarcinoma
Homo sapiens (human)
DOID:437
  • myasthenia gravis
Homo sapiens (human)
DOID:0110306
  • autosomal dominant limb-girdle muscular dystrophy type 3
  • Aliases:
    • LGMD1G
    • autosomal dominant limb-girdle muscular dystrophy type 1G
    • muscular dystrophy limb-girdle type 1G
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