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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources October 9, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 12451 - 12475 of 15957 in total
Disease ID Disease Name ▲ Gene Symbol Gene ID Organism Source
DOID:0070344
  • ocular tuberculosis
Rattus norvegicus (Norway rat)
DOID:0070344
  • ocular tuberculosis
Homo sapiens (human)
DOID:0060482
  • oculoauricular syndrome
Homo sapiens (human)
DOID:1056
  • oculocerebrorenal syndrome
  • Aliases:
    • Lowe syndrome
    • lowe oculocerebrorenal syndrome
    • oculocerebrorenal syndrome of Lowe
Homo sapiens (human)
DOID:0070094
  • oculocutaneous albinism type IA
  • Aliases:
    • OCA1A
    • Oculocutaneous Albinism, Tyrosinase-Negative
Caenorhabditis elegans
DOID:0070094
  • oculocutaneous albinism type IA
  • Aliases:
    • OCA1A
    • Oculocutaneous Albinism, Tyrosinase-Negative
Mus musculus (house mouse)
DOID:0070094
  • oculocutaneous albinism type IA
  • Aliases:
    • OCA1A
    • Oculocutaneous Albinism, Tyrosinase-Negative
Homo sapiens (human)
DOID:0070095
  • oculocutaneous albinism type IB
  • Aliases:
    • Albinism, Yellow Mutant Type
    • OCA1B
Mus musculus (house mouse)
DOID:0070095
  • oculocutaneous albinism type IB
  • Aliases:
    • Albinism, Yellow Mutant Type
    • OCA1B
Caenorhabditis elegans
DOID:0070095
  • oculocutaneous albinism type IB
  • Aliases:
    • Albinism, Yellow Mutant Type
    • OCA1B
Homo sapiens (human)
DOID:0070096
  • oculocutaneous albinism type II
  • Aliases:
    • OCA2
    • Oculocutaneous Albinism, Tyrosinase-Positive
Homo sapiens (human)
DOID:0070096
  • oculocutaneous albinism type II
  • Aliases:
    • OCA2
    • Oculocutaneous Albinism, Tyrosinase-Positive
Mus musculus (house mouse)
DOID:0070097
  • oculocutaneous albinism type III
  • Aliases:
    • OCA3
    • Rufous Oculocutaneous Albinism
Mus musculus (house mouse)
DOID:0070097
  • oculocutaneous albinism type III
  • Aliases:
    • OCA3
    • Rufous Oculocutaneous Albinism
Homo sapiens (human)
DOID:0070097
  • oculocutaneous albinism type III
  • Aliases:
    • OCA3
    • Rufous Oculocutaneous Albinism
Caenorhabditis elegans
DOID:0070098
  • oculocutaneous albinism type IV
  • Aliases:
    • OCA4
Homo sapiens (human)
DOID:0070098
  • oculocutaneous albinism type IV
  • Aliases:
    • OCA4
Mus musculus (house mouse)
DOID:0050632
  • oculocutaneous albinism
Caenorhabditis elegans
DOID:0050632
  • oculocutaneous albinism
Mus musculus (house mouse)
DOID:0050632
  • oculocutaneous albinism
Homo sapiens (human)
DOID:0060291
  • oculodentodigital dysplasia
  • Aliases:
    • ODD syndrome
Mus musculus (house mouse)
DOID:0111705
  • oculoectodermal syndrome
  • Aliases:
    • Toriello-Lacassie-Droste syndrome
    • aplasia cutis congenita-epibulbar dermoids syndrome
Mus musculus (house mouse)
DOID:0111705
  • oculoectodermal syndrome
  • Aliases:
    • Toriello-Lacassie-Droste syndrome
    • aplasia cutis congenita-epibulbar dermoids syndrome
Homo sapiens (human)
DOID:11719
  • oculopharyngeal muscular dystrophy
  • Aliases:
    • Muscular dystrophy, oculopharyngeal
Homo sapiens (human)
DOID:0081297
  • oculopharyngodistal myopathy 1
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: December 9, 2024