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 2851 - 2875 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism
DOID:0060071
  • pre-malignant neoplasm
Homo sapiens (human)
DOID:13452
  • scleritis
Homo sapiens (human)
DOID:0050851
  • glomerulosclerosis
Homo sapiens (human)
DOID:4449
  • macular retinal edema
  • Aliases:
    • macular edema
    • macular oedema
    • macular retinal oedema
Homo sapiens (human)
DOID:4447
  • cystoid macular edema
Homo sapiens (human)
DOID:10272
  • left bundle branch hemiblock
  • Aliases:
    • Left bundle branch block
Homo sapiens (human)
DOID:0050662
  • bestrophinopathy
  • Aliases:
    • autosomal recessive bestrophinopathy
Homo sapiens (human)
DOID:4331
  • burning mouth syndrome
  • Aliases:
    • Orodynia
    • Stomatopyrosis
Homo sapiens (human)
DOID:9820
  • central gyrate choroidal dystrophy
  • Aliases:
    • Choroidal dystrophy, serpiginous
Homo sapiens (human)
DOID:2983
  • anuria
  • Aliases:
    • Suppression of urinary secretion
Homo sapiens (human)
DOID:0111131
  • focal segmental glomerulosclerosis 6
  • Aliases:
    • FSGS6
Homo sapiens (human)
DOID:0060610
  • megacystis-microcolon-intestinal hypoperistalsis syndrome
  • Aliases:
    • Berdon syndrome
    • Megacystis microcolon intestinal hypoperistalsis syndrome
    • megacystis-microcolon-intestinal hypoperistalsis syndrome, MMIH
    • visceral myopathy
Homo sapiens (human)
DOID:0111128
  • focal segmental glomerulosclerosis 1
  • Aliases:
    • FSGS1
Homo sapiens (human)
DOID:0111129
  • focal segmental glomerulosclerosis 2
  • Aliases:
    • FSGS2
Homo sapiens (human)
DOID:0111130
  • focal segmental glomerulosclerosis 5
  • Aliases:
    • FSGS5
Homo sapiens (human)
DOID:0060550
  • ablepharon macrostomia syndrome
Homo sapiens (human)
DOID:0111425
  • restrictive cardiomyopathy 1
  • Aliases:
    • RCM1
    • familial restrictive cardiomyopathy 1
Homo sapiens (human)
DOID:0111133
  • focal segmental glomerulosclerosis 8
  • Aliases:
    • FSGS8
Homo sapiens (human)
DOID:0111134
  • focal segmental glomerulosclerosis 9
  • Aliases:
    • FSGS9
Homo sapiens (human)
DOID:0050864
  • non-arteritic anterior ischemic optic neuropathy
  • Aliases:
    • non-arteritic anterior ischaemic optic neuropathy
    • nonarteritic anterior ischaemic optic neuropathy
    • nonarteritic anterior ischemic optic neuropathy
Homo sapiens (human)
DOID:13364
  • obsolete chronobiology disease
Homo sapiens (human)
DOID:10322
  • berylliosis
  • Aliases:
    • beryllium poisoning
Homo sapiens (human)
DOID:0111132
  • focal segmental glomerulosclerosis 7
  • Aliases:
    • FSGS7
Homo sapiens (human)
DOID:701
  • dentin dysplasia
  • Aliases:
    • Dentinal dysplasia
Homo sapiens (human)
DOID:0110058
  • amelogenesis imperfecta type 1E
  • Aliases:
    • AIH1
    • X-linked amelogenesis imperfecta 1
    • X-linked amelogenesis imperfecta hypoplastic/hypomaturation 1
    • amelogenesis imperfecta hypomaturationtype with snow-capped teeth
    • amelogenesis imperfecta type IE
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