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 1501 - 1525 of 7942 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism
DOID:540
  • strabismus
Homo sapiens (human)
DOID:9837
  • hypertropia
Homo sapiens (human)
DOID:9306
  • mechanical strabismus
Homo sapiens (human)
DOID:9650
  • pathologic nystagmus
Homo sapiens (human)
DOID:11771
  • spontaneous ocular nystagmus
  • Aliases:
    • Ocular nystagmus
    • Searching eye movements
    • visual deprivation nystagmus
Homo sapiens (human)
DOID:13174
  • dissociated nystagmus
Homo sapiens (human)
DOID:9649
  • congenital nystagmus
Homo sapiens (human)
DOID:5723
  • optic atrophy
  • Aliases:
    • atrophy of optic disc
Homo sapiens (human)
DOID:0050564
  • autosomal dominant nonsyndromic deafness
  • Aliases:
    • autosomal dominant deafness
Homo sapiens (human)
DOID:0050566
  • X-linked nonsyndromic deafness
  • Aliases:
    • X-linked deafness
Homo sapiens (human)
DOID:0110498
  • autosomal recessive nonsyndromic deafness 4
  • Aliases:
    • DFNB4
    • autosomal recessive deafness 4 with enlarged vestibular aqueduct
Homo sapiens (human)
DOID:0050565
  • autosomal recessive nonsyndromic deafness
Homo sapiens (human)
DOID:0110524
  • autosomal recessive nonsyndromic deafness 76
  • Aliases:
    • DFNB76
    • autosomal recessive deafness 76
Homo sapiens (human)
DOID:0110493
  • autosomal recessive nonsyndromic deafness 35
  • Aliases:
    • DFNB35
    • autosomal recessive deafness 35
Homo sapiens (human)
DOID:0110526
  • autosomal recessive nonsyndromic deafness 79
  • Aliases:
    • DFNB79
    • autosomal recessive deafness 79
Homo sapiens (human)
DOID:0110539
  • autosomal recessive nonsyndromic deafness 97
  • Aliases:
    • DFNB97
    • autosomal recessive deafness 97
Homo sapiens (human)
DOID:0110487
  • autosomal recessive nonsyndromic deafness 29
  • Aliases:
    • DFNB29
    • autosomal recessive deafness 29
Homo sapiens (human)
DOID:0110496
  • autosomal recessive nonsyndromic deafness 38
  • Aliases:
    • DFNB38
    • autosomal recessive deafness 38
Homo sapiens (human)
DOID:0110476
  • autosomal recessive nonsyndromic deafness 1B
  • Aliases:
    • DFNB1B
    • autosomal recessive deafness 1B
Homo sapiens (human)
DOID:0110532
  • autosomal recessive nonsyndromic deafness 86
  • Aliases:
    • DFNB86
    • autosomal recessive deafness 86
Homo sapiens (human)
DOID:0110505
  • autosomal recessive nonsyndromic deafness 48
  • Aliases:
    • DFNB48
    • autosomal recessive deafness 48
Homo sapiens (human)
DOID:0110537
  • autosomal recessive nonsyndromic deafness 93
  • Aliases:
    • DFNB93
    • autosomal recessive deafness 93
Homo sapiens (human)
DOID:0110507
  • autosomal recessive nonsyndromic deafness 5
  • Aliases:
    • DFNB5
    • autosomal recessive deafness 5
Homo sapiens (human)
DOID:0110480
  • autosomal recessive nonsyndromic deafness 22
  • Aliases:
    • DFNB22
    • autosomal recessive deafness 22
Homo sapiens (human)
DOID:0110514
  • autosomal recessive nonsyndromic deafness 62
  • Aliases:
    • DFNB62
    • autosomal recessive deafness 62
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