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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 7426 - 7450 of 15957 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism Source
DOID:0111364
  • Alzheimer's disease 9
  • Aliases:
    • AD9
    • Alzheimer's disease 9, late onset
Homo sapiens (human)
DOID:0111364
  • Alzheimer's disease 9
  • Aliases:
    • AD9
    • Alzheimer's disease 9, late onset
Caenorhabditis elegans
DOID:0111365
  • benign familial hematuria
  • Aliases:
    • BFH
    • TMN
    • thin basement membrane nephropathy
    • thin membrane nephropathy
Mus musculus (house mouse)
DOID:0111365
  • benign familial hematuria
  • Aliases:
    • BFH
    • TMN
    • thin basement membrane nephropathy
    • thin membrane nephropathy
Drosophila melanogaster (fruit fly)
DOID:0111365
  • benign familial hematuria
  • Aliases:
    • BFH
    • TMN
    • thin basement membrane nephropathy
    • thin membrane nephropathy
Homo sapiens (human)
DOID:0111366
  • familial hepatic adenoma
  • Aliases:
    • familial liver cell adenomas
Homo sapiens (human)
DOID:0111369
  • hyperalphalipoproteinemia 1
  • Aliases:
    • HALP1
Homo sapiens (human)
DOID:0111370
  • apolipoprotein C-III deficiency
  • Aliases:
    • HALP2
    • hyperalphalipoproteinemia 2
Homo sapiens (human)
DOID:0111370
  • apolipoprotein C-III deficiency
  • Aliases:
    • HALP2
    • hyperalphalipoproteinemia 2
Mus musculus (house mouse)
DOID:0111371
  • isolated hyperchlorhidrosis
  • Aliases:
    • HYCHL
    • carbonic anhydrase XII deficiency
Homo sapiens (human)
DOID:0111371
  • isolated hyperchlorhidrosis
  • Aliases:
    • HYCHL
    • carbonic anhydrase XII deficiency
Mus musculus (house mouse)
DOID:0111373
  • familial progressive hyperpigmentation with or without hypopigmentation
  • Aliases:
    • FPHH
    • MUH
    • melanosis universalis hereditaria
Rattus norvegicus (Norway rat)
DOID:0111373
  • familial progressive hyperpigmentation with or without hypopigmentation
  • Aliases:
    • FPHH
    • MUH
    • melanosis universalis hereditaria
Mus musculus (house mouse)
DOID:0111373
  • familial progressive hyperpigmentation with or without hypopigmentation
  • Aliases:
    • FPHH
    • MUH
    • melanosis universalis hereditaria
Homo sapiens (human)
DOID:0111376
  • fetal akinesia deformation sequence syndrome 3
  • Aliases:
    • FADS3
Homo sapiens (human)
DOID:0111377
  • fetal akinesia deformation sequence syndrome 1
  • Aliases:
    • FADS1
Rattus norvegicus (Norway rat)
DOID:0111377
  • fetal akinesia deformation sequence syndrome 1
  • Aliases:
    • FADS1
Homo sapiens (human)
DOID:0111377
  • fetal akinesia deformation sequence syndrome 1
  • Aliases:
    • FADS1
Mus musculus (house mouse)
DOID:0111377
  • fetal akinesia deformation sequence syndrome 1
  • Aliases:
    • FADS1
Drosophila melanogaster (fruit fly)
DOID:0111380
  • solitary median maxillary central incisor
  • Aliases:
    • SMMCI
    • fused incisors
    • single central maxillary incisor
    • single median maxillary central incisor
    • single upper central incisor
Mus musculus (house mouse)
DOID:0111380
  • solitary median maxillary central incisor
  • Aliases:
    • SMMCI
    • fused incisors
    • single central maxillary incisor
    • single median maxillary central incisor
    • single upper central incisor
Caenorhabditis elegans
DOID:0111380
  • solitary median maxillary central incisor
  • Aliases:
    • SMMCI
    • fused incisors
    • single central maxillary incisor
    • single median maxillary central incisor
    • single upper central incisor
Rattus norvegicus (Norway rat)
DOID:0111380
  • solitary median maxillary central incisor
  • Aliases:
    • SMMCI
    • fused incisors
    • single central maxillary incisor
    • single median maxillary central incisor
    • single upper central incisor
Homo sapiens (human)
DOID:0111381
  • IVIC syndrome
  • Aliases:
    • Instituto Venezolano de Investigaciones Cientificas syndrome
    • OORS
    • Oculootoradial syndrome
    • oculo-oto-radial syndrome
    • radial ray defects, hearing impairment, external ophthalmoplegia, and thrombocytopenia
Mus musculus (house mouse)
DOID:0111381
  • IVIC syndrome
  • Aliases:
    • Instituto Venezolano de Investigaciones Cientificas syndrome
    • OORS
    • Oculootoradial syndrome
    • oculo-oto-radial syndrome
    • radial ray defects, hearing impairment, external ophthalmoplegia, and thrombocytopenia
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: December 9, 2024