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 4226 - 4250 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism
DOID:13413
  • hepatic encephalopathy
  • Aliases:
    • Portal-systemic encephalopathy
Saccharomyces cerevisiae S288C
DOID:0110645
  • long QT syndrome 2
  • Aliases:
    • LQT2
Saccharomyces cerevisiae S288C
DOID:7575
  • pancreatic intraductal papillary-mucinous neoplasm
Homo sapiens (human)
DOID:8670
  • eating disorder
Homo sapiens (human)
DOID:2368
  • gangliosidosis
Homo sapiens (human)
DOID:4210
  • clear cell meningioma
Homo sapiens (human)
DOID:0090142
  • cystathioninuria
  • Aliases:
    • cystathionase deficiency
    • cystathione gamma-lyase deficiency syndrome
    • gamma-cystathionase deficiency
Homo sapiens (human)
DOID:576
  • proteinuria
Mus musculus (house mouse)
DOID:612
  • primary immunodeficiency disease
  • Aliases:
    • hypoimmunity
    • immune deficiency disorder
    • immunodeficiency syndrome
Saccharomyces cerevisiae S288C
DOID:0080220
  • obsolete major affective disorder 1
Homo sapiens (human)
DOID:0050731
  • vitamin B12 deficiency
  • Aliases:
    • cobalamin deficiency
    • hypocobalaminemia
Xenopus tropicalis (tropical clawed frog)
DOID:12895
  • keratoconjunctivitis sicca
  • Aliases:
    • KCS
Rattus norvegicus (Norway rat)
DOID:0110284
  • autosomal recessive limb-girdle muscular dystrophy type 2L
  • Aliases:
    • LGMD2L
    • muscular dystrophy, limb-girdle, type 2L
Rattus norvegicus (Norway rat)
DOID:0110847
  • xeroderma pigmentosum variant type
  • Aliases:
    • XPV
    • photosensitivity with defective DNA synthesis
    • xeroderma pigmentosum with normal DNA repair rates
Homo sapiens (human)
DOID:4194
  • glucose metabolism disease
  • Aliases:
    • disorder of glucose metabolism
Saccharomyces cerevisiae S288C
DOID:9869
  • hereditary fructose intolerance syndrome
  • Aliases:
    • Fructosaemia
    • Fructose-1,6-bisphosphate aldolase B deficiency
    • Fructosemia
Drosophila melanogaster (fruit fly)
DOID:13778
  • chancroid
  • Aliases:
    • Ulcus molle, skin
Homo sapiens (human)
DOID:594
  • panic disorder
  • Aliases:
    • panic anxiety syndrome
Homo sapiens (human)
DOID:0050117
  • disease by infectious agent
  • Aliases:
    • infectious disease
Homo sapiens (human)
DOID:5695
  • childhood liposarcoma
  • Aliases:
    • pediatric liposarcoma
Homo sapiens (human)
DOID:12359
  • endocrine exophthalmos
Homo sapiens (human)
DOID:0060692
  • platelet-type bleeding disorder 8
  • Aliases:
    • ADP platelet receptor P2Y12 defect
    • P2Y12 defect
Homo sapiens (human)
DOID:2411
  • granular cell tumor
  • Aliases:
    • neoplasm of granular cell
Homo sapiens (human)
DOID:13359
  • Ehlers-Danlos syndrome
  • Aliases:
    • Cutis hyperelastica
    • elastic skin
Xenopus tropicalis (tropical clawed frog)
DOID:0110741
  • type 1 diabetes mellitus 2
  • Aliases:
    • IDDM2
    • Insulin-Dependent Diabetes Mellitus 2
Xenopus laevis (African clawed frog)

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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