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 1801 - 1825 of 7942 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism
DOID:0050632
  • oculocutaneous albinism
Homo sapiens (human)
DOID:0070094
  • oculocutaneous albinism type IA
  • Aliases:
    • OCA1A
    • Oculocutaneous Albinism, Tyrosinase-Negative
Homo sapiens (human)
DOID:1056
  • oculocerebrorenal syndrome
  • Aliases:
    • Lowe syndrome
    • lowe oculocerebrorenal syndrome
    • oculocerebrorenal syndrome of Lowe
Homo sapiens (human)
DOID:1752
  • ocular melanoma
  • Aliases:
    • eye melanoma
    • intraocular melanoma
    • melanoma of eye
Homo sapiens (human)
DOID:790
  • ocular hypotension
  • Aliases:
    • Hypotony of eye
Homo sapiens (human)
DOID:9282
  • ocular hypertension
Rattus norvegicus (Norway rat)
DOID:9282
  • ocular hypertension
Xenopus tropicalis (tropical clawed frog)
DOID:9282
  • ocular hypertension
Saccharomyces cerevisiae S288C
DOID:9282
  • ocular hypertension
Homo sapiens (human)
DOID:9282
  • ocular hypertension
Danio rerio (zebrafish)
DOID:9282
  • ocular hypertension
Mus musculus (house mouse)
DOID:9282
  • ocular hypertension
Drosophila melanogaster (fruit fly)
DOID:2174
  • ocular cancer
  • Aliases:
    • Ocular tumor
    • eye neoplasm
    • malignant eye neoplasm
    • neoplasm of eye
    • neoplasm of eye proper
Homo sapiens (human)
DOID:0090100
  • ocular albinism with sensorineural deafness
  • Aliases:
    • WS2-OA
    • autosomal recessive Waardenburg syndrome type 2 with ocular albinism
    • digenic Waardenburg syndrome/albinism
    • digenic Waardenburg syndrome/ocular albinism
Homo sapiens (human)
DOID:0050633
  • ocular albinism 1
  • Aliases:
    • Albinism ocular 1
    • ocular albinism
Homo sapiens (human)
DOID:14223
  • ochronosis
Homo sapiens (human)
DOID:4404
  • occupational dermatitis
  • Aliases:
    • Occupational allergic contact dermatitis
    • Occupational eczema
Homo sapiens (human)
DOID:0111272
  • occipital horn syndrome
  • Aliases:
    • EDS IX
    • Ehlers-Danlos syndrome type 9
    • Ehlers-Danlos syndrome type IX
    • X-linked cutis laxa
Homo sapiens (human)
DOID:0050848
  • obstructive sleep apnea
  • Aliases:
    • obstructive sleep apnea syndrome
Mus musculus (house mouse)
DOID:0050848
  • obstructive sleep apnea
  • Aliases:
    • obstructive sleep apnea syndrome
Homo sapiens (human)
DOID:0050848
  • obstructive sleep apnea
  • Aliases:
    • obstructive sleep apnea syndrome
Rattus norvegicus (Norway rat)
DOID:0070314
  • obstructive nephropathy
  • Aliases:
    • CON
    • congenital obstructive nephropathy
Homo sapiens (human)
DOID:2320
  • obstructive lung disease
  • Aliases:
    • respiratory airway obstruction
Homo sapiens (human)
DOID:13603
  • obstructive jaundice
  • Aliases:
    • Cholestatic Jaundice
    • Cholestatic jaundice syndrome
    • Obstructive hyperbilirubinemia
Mus musculus (house mouse)
DOID:13603
  • obstructive jaundice
  • Aliases:
    • Cholestatic Jaundice
    • Cholestatic jaundice syndrome
    • Obstructive hyperbilirubinemia
Rattus norvegicus (Norway rat)

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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