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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 11426 - 11450 of 15957 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism Source
DOID:0080077
  • hypophosphatemic nephrolithiasis/osteoporosis 1
Mus musculus (house mouse)
DOID:0050336
  • hypophosphatemia
Mus musculus (house mouse)
DOID:0080758
  • Fanconi renotubular syndrome 2
Mus musculus (house mouse)
DOID:0050947
  • hereditary hypophosphatemic rickets with hypercalciuria
Rattus norvegicus (Norway rat)
DOID:0080077
  • hypophosphatemic nephrolithiasis/osteoporosis 1
Rattus norvegicus (Norway rat)
DOID:0080758
  • Fanconi renotubular syndrome 2
Rattus norvegicus (Norway rat)
DOID:0050336
  • hypophosphatemia
Rattus norvegicus (Norway rat)
DOID:12117
  • pulmonary alveolar microlithiasis
Mus musculus (house mouse)
DOID:12117
  • pulmonary alveolar microlithiasis
Rattus norvegicus (Norway rat)
DOID:0070388
  • developmental and epileptic encephalopathy 102
  • Aliases:
    • DEE102
    • early infantile epileptic encephalopathy 102
Rattus norvegicus (Norway rat)
DOID:0070388
  • developmental and epileptic encephalopathy 102
  • Aliases:
    • DEE102
    • early infantile epileptic encephalopathy 102
Mus musculus (house mouse)
DOID:0080537
  • hypermanganesemia with dystonia 2
Mus musculus (house mouse)
DOID:0050605
  • acrodermatitis enteropathica
Rattus norvegicus (Norway rat)
DOID:0050605
  • acrodermatitis enteropathica
Mus musculus (house mouse)
DOID:0060480
  • left ventricular noncompaction
  • Aliases:
    • left ventricular hypertrabeculation
Rattus norvegicus (Norway rat)
DOID:0070266
  • congenital disorder of glycosylation type IIn
  • Aliases:
    • CDG IIn
    • CDG syndrome type IIn
    • CDG2N
    • CDGIIdn
    • Carbohydrate deficient glycoprotein syndrome type IIn
    • Congenital disorder of glycosylation type 2n
    • SLC39A8-CDG
Rattus norvegicus (Norway rat)
DOID:0070266
  • congenital disorder of glycosylation type IIn
  • Aliases:
    • CDG IIn
    • CDG syndrome type IIn
    • CDG2N
    • CDGIIdn
    • Carbohydrate deficient glycoprotein syndrome type IIn
    • Congenital disorder of glycosylation type 2n
    • SLC39A8-CDG
Mus musculus (house mouse)
DOID:9266
  • cystinuria
Mus musculus (house mouse)
DOID:9266
  • cystinuria
Rattus norvegicus (Norway rat)
DOID:0080899
  • lung pleomorphic carcinoma
Mus musculus (house mouse)
DOID:0080899
  • lung pleomorphic carcinoma
Rattus norvegicus (Norway rat)
DOID:0111028
  • hemochromatosis type 4
  • Aliases:
    • HFE4
    • autosomal dominant hereditary hemochromatosis
    • ferroportin disease
    • hemochromatosis due to defect in ferroportin
Mus musculus (house mouse)
DOID:0080268
  • autosomal dominant nonsyndromic deafness 72
Rattus norvegicus (Norway rat)
DOID:0080268
  • autosomal dominant nonsyndromic deafness 72
Mus musculus (house mouse)
DOID:0070098
  • oculocutaneous albinism type IV
  • Aliases:
    • OCA4
Mus musculus (house mouse)
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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