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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 1476 - 1500 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0112318
  • Schindler disease type 1
  • Aliases:
    • NAGA deficiency type 1
    • alpha-N-acetylgalactosaminidase deficiency type 1
Homo sapiens (human)
DOID:5154
  • borna disease
  • Aliases:
    • Enzootic encephalomyelitis
Mus musculus (house mouse)
DOID:0110923
  • familial hemophagocytic lymphohistiocytosis 3
  • Aliases:
    • FHL3
    • HLH3
    • HPLH3
Homo sapiens (human)
DOID:0080201
  • Peters plus syndrome
  • Aliases:
    • Krause-Kivlin syndrome
    • Peters anomaly-short limb dwarfism syndrome
    • Peters-plus syndrome
Homo sapiens (human)
DOID:0050557
  • congenital muscular dystrophy
Rattus norvegicus (Norway rat)
DOID:0111814
  • methylmalonic acidemia and homocysteinemia cblX type
  • Aliases:
    • combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblX
    • mental retardation, X-linked 3
    • methylmalonic aciduria with homocystinuria, type cblX
Mus musculus (house mouse)
DOID:0110340
  • osteogenesis imperfecta type 4
  • Aliases:
    • OI4
    • osteogenesis imperfecta type IV
    • osteogenesis imperfecta with normal sclera
Homo sapiens (human)
DOID:1307
  • dementia
Saccharomyces cerevisiae S288C
DOID:0080201
  • Peters plus syndrome
  • Aliases:
    • Krause-Kivlin syndrome
    • Peters anomaly-short limb dwarfism syndrome
    • Peters-plus syndrome
Rattus norvegicus (Norway rat)
DOID:0060703
  • Muenke Syndrome
  • Aliases:
    • FGFR3-related craniosynostosis
Homo sapiens (human)
DOID:9352
  • type 2 diabetes mellitus
  • Aliases:
    • NIDDM
    • insulin resistance
    • non-insulin-dependent diabetes mellitus
    • type 2 diabetes
    • type II diabetes mellitus
Danio rerio (zebrafish)
DOID:0080204
  • renal hypoplasia
Xenopus laevis (African clawed frog)
DOID:0080948
  • agenesis of corpus callosum, cardiac, ocular, and genital syndrome
Danio rerio (zebrafish)
DOID:2215
  • factor VII deficiency
  • Aliases:
    • deficiency, stable
Mus musculus (house mouse)
DOID:0110704
  • hypotrichosis 7
  • Aliases:
    • Hypt7
    • Lah2
    • hypotrichosis, localized, autosomal recessive 2
    • total Mari type hypotrichosis,
Danio rerio (zebrafish)
DOID:898
  • autosomal dominant polycystic kidney disease
  • Aliases:
    • ADPKD
    • Congenital biliary ectasias
    • POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1
Rattus norvegicus (Norway rat)
DOID:9065
  • leishmaniasis
Rattus norvegicus (Norway rat)
DOID:3877
  • functional colonic disease
Homo sapiens (human)
DOID:0112007
  • growth hormone secreting pituitary adenoma 2
  • Aliases:
    • GH-secreting pituitary adenoma 2
    • PITA2
    • X-linked acromegaly
    • acromegaly due to pituitary adenoma 2
Mus musculus (house mouse)
DOID:0080573
  • congenital disorder of glycosylation Ix
  • Aliases:
    • congenital disorder of glycosylation 1x
Caenorhabditis elegans
DOID:0050457
  • Sertoli cell-only syndrome
  • Aliases:
    • DEL CASTILLO SYNDROME
    • Germinal Cell Aplasia
Homo sapiens (human)
DOID:3263
  • piebaldism
  • Aliases:
    • PIEBALD TRAIT
    • Partial albinism
Xenopus laevis (African clawed frog)
DOID:643
  • progressive multifocal leukoencephalopathy
Homo sapiens (human)
DOID:0080264
  • exudative vitreoretinopathy 7
  • Aliases:
    • EVR7
Mus musculus (house mouse)
DOID:0060246
  • MASA syndrome
  • Aliases:
    • CRASH syndrome
    • Gareis-Mason syndrome
    • L1 syndrome
    • SPG1
    • X-linked complicated hereditary spastic paraplegia type 1
    • X-linked corpus callosum agenesis
    • X-linked spastic paraplegia 1
    • hereditary spastic paraplegia 1
Caenorhabditis elegans
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Last updated: December 9, 2024