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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 7626 - 7650 of 15957 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism Source
DOID:4677
  • keratitis
Homo sapiens (human)
DOID:9402
  • epididymitis
Homo sapiens (human)
DOID:12835
  • quadriplegia
  • Aliases:
    • tetraplegia
Homo sapiens (human)
DOID:13593
  • eclampsia
  • Aliases:
    • Eclampsia in puerperium
    • Eclampsia, postpartum
    • Postpartum eclampsia
Homo sapiens (human)
DOID:319
  • spinal cord disease
Homo sapiens (human)
DOID:0080545
  • hyper IgE syndrome
  • Aliases:
    • hyper immunoglobulin E syndrome
Homo sapiens (human)
DOID:11613
  • hyperandrogenism
  • Aliases:
    • hyperandrogenization syndrome
Homo sapiens (human)
DOID:0080596
  • hyper IgE recurrent infection syndrome 4
Homo sapiens (human)
DOID:13777
  • epidermodysplasia verruciformis
Homo sapiens (human)
DOID:0110500
  • autosomal recessive nonsyndromic deafness 42
  • Aliases:
    • DFNB42
    • autosomal recessive deafness 42
Homo sapiens (human)
DOID:9266
  • cystinuria
Saccharomyces cerevisiae S288C
DOID:0112202
  • developmental and epileptic encephalopathy
Saccharomyces cerevisiae S288C
DOID:0081421
  • familial focal epilepsy with variable foci 1
Saccharomyces cerevisiae S288C
DOID:0081423
  • familial focal epilepsy with variable foci 3
Saccharomyces cerevisiae S288C
DOID:2234
  • focal epilepsy
  • Aliases:
    • localisation-related epilepsy
    • partial epilepsy
Saccharomyces cerevisiae S288C
DOID:0081221
  • autosomal recessive intellectual developmental disorder 59
Homo sapiens (human)
DOID:0050661
  • vitelliform macular dystrophy
  • Aliases:
    • Best disease
    • Best macular dystrophy
    • juvenile-onset vitelliform macular dystrophy
Homo sapiens (human)
DOID:0110371
  • retinitis pigmentosa 56
  • Aliases:
    • RP56
Homo sapiens (human)
DOID:0112155
  • inflammatory bowel disease 29
  • Aliases:
    • IBD29
Homo sapiens (human)
DOID:0110205
  • Charcot-Marie-Tooth disease dominant intermediate E
  • Aliases:
    • CMTDIE
    • Charcot-Marie-Tooth disease-nephropathy syndrome
    • Charcot-Marie-Tooth neuropathy with focal segmental glomerulonephritis
    • autosomal dominant intermediate Charcot-Marie-Tooth disease type E
Homo sapiens (human)
DOID:0111130
  • focal segmental glomerulosclerosis 5
  • Aliases:
    • FSGS5
Homo sapiens (human)
DOID:2997
  • Sertoli-Leydig cell tumor
Homo sapiens (human)
DOID:0060894
  • early-onset Parkinson's disease
  • Aliases:
    • early-onset Parkinson disease
Saccharomyces cerevisiae S288C
DOID:14250
  • Down syndrome
  • Aliases:
    • Complete trisomy 21 syndrome
    • Down's syndrome
    • Down's syndrome - trisomy 21
    • Downs syndrome
    • G Trisomy
    • trisomy 21 syndrome
Saccharomyces cerevisiae S288C
DOID:0080464
  • developmental and epileptic encephalopathy 53
  • Aliases:
    • DEE53
    • early infantile epileptic encephalopathy 53
Saccharomyces cerevisiae S288C
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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