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 4776 - 4800 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼ Source
DOID:1925
  • Coffin-Siris syndrome
  • Aliases:
    • Dwarfism-Onychodysplasia
    • Fifth Digit Syndrome
    • Short Stature-Onychodysplasia.
Homo sapiens (human)
DOID:0070352
  • stress-induced childhood-onset neurodegeneration with variable ataxia and seizures
  • Aliases:
    • CONDSIAS
Homo sapiens (human)
DOID:8867
  • molluscum contagiosum
Homo sapiens (human)
DOID:0070269
  • congenital disorder of glycosylation type IIq
  • Aliases:
    • CDG IIq
    • CDG2Q
    • CDGIIdq
    • COG2-CDG
    • COG2-related congenital disorder of glycosylation
Homo sapiens (human)
DOID:0080110
  • contractures, pterygia, and spondylocarpotarsal fusion syndrome
  • Aliases:
    • multiple pterygium syndrome
Homo sapiens (human)
DOID:0080721
  • calvarial doughnut lesions with bone fragility
Homo sapiens (human)
DOID:1574
  • alcohol use disorder
  • Aliases:
    • Ethanol abuse
    • alcohol abuse
Homo sapiens (human)
DOID:5160
  • arteriosclerosis obliterans
Homo sapiens (human)
DOID:898
  • autosomal dominant polycystic kidney disease
  • Aliases:
    • ADPKD
    • Congenital biliary ectasias
    • POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1
Homo sapiens (human)
DOID:4762
  • vasculogenic impotence
Homo sapiens (human)
DOID:0090061
  • familial cold autoinflammatory syndrome
  • Aliases:
    • FCAS
Homo sapiens (human)
DOID:4137
  • common bile duct disease
Homo sapiens (human)
DOID:2600
  • laryngeal carcinoma
  • Aliases:
    • cancer of larynx
    • carcinoma of larynx
Homo sapiens (human)
DOID:0110053
  • amelogenesis imperfecta type 4
  • Aliases:
    • AI4
    • AIHHT
    • amelogenesis imperfecta hypomaturation-hypoplastic type with taurodontism
Homo sapiens (human)
DOID:0110153
  • Charcot-Marie-Tooth disease type 1E
  • Aliases:
    • CMT1E
    • Charcot-Marie-Tooth disease and deafness
    • Charcot-Marie-Tooth disease demyelinating type 1E
    • Charcot-Marie-Tooth disease-deafness
    • autosomal dominant Charcot-Marie-Tooth neuropathy and deafness
Homo sapiens (human)
DOID:11054
  • urinary bladder cancer
  • Aliases:
    • bladder cancer
    • tumor of the bladder
Homo sapiens (human)
DOID:0050083
  • Keshan disease
Homo sapiens (human)
DOID:3070
  • high grade glioma
  • Aliases:
    • Neuroglial tumor
    • glial cell tumor
    • glioma, malignant
    • malignant Neuroglial tumor
    • malignant glioma
Homo sapiens (human)
DOID:0112219
  • developmental and epileptic encephalopathy 84
  • Aliases:
    • DEE84
    • Jamuar syndrome
    • early infantile epileptic encephalopathy 84
Homo sapiens (human)
DOID:3052
  • Balkan nephropathy
  • Aliases:
    • Balkan endemic nephropathy
    • DEFN
    • Danubian endemic familial nephropathy
Homo sapiens (human)
DOID:4607
  • biliary tract cancer
  • Aliases:
    • malignant tumour of biliary tract
Homo sapiens (human)
DOID:4776
  • rapidly progressive glomerulonephritis
Homo sapiens (human)
DOID:1584
  • acute chest syndrome
  • Aliases:
    • acute chest syndrome in sickle cell disease
Homo sapiens (human)
DOID:0111130
  • focal segmental glomerulosclerosis 5
  • Aliases:
    • FSGS5
Homo sapiens (human)
DOID:2449
  • acromegaly
Homo sapiens (human)

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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