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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 551 - 575 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:9402
  • epididymitis
Rattus norvegicus (Norway rat)
DOID:0080561
  • congenital disorder of glycosylation Ii
  • Aliases:
    • congenital disorder of glycosylation 1i
Xenopus laevis (African clawed frog)
DOID:0110176
  • Charcot-Marie-Tooth disease axonal type 2X
  • Aliases:
    • Charcot-Marie-Tooth neuropathy type 2X
    • autosomal recessive axonal Charcot-Marie-Tooth disease type 2X
Homo sapiens (human)
DOID:0060835
  • isolated microphthalmia 6
  • Aliases:
    • MCOP6
    • posterior nonsyndromic microphthalmia
Homo sapiens (human)
DOID:0050719
  • cerebral folate receptor alpha deficiency
  • Aliases:
    • Neurodegeneration due to cerebral folate transport deficiency
Mus musculus (house mouse)
DOID:0110806
  • hereditary spastic paraplegia 54
  • Aliases:
    • SPG54
    • autosomal recessive spastic paraplegia 54
    • autosomal recessive spastic paraplegia type 54
Homo sapiens (human)
DOID:13399
  • color blindness
  • Aliases:
    • BLINDNESS COLOR
    • Colour blindness
    • Colour vision deficiency
Mus musculus (house mouse)
DOID:14566
  • disease of cellular proliferation
  • Aliases:
    • cell process disease
    • neoplasm
Homo sapiens (human)
DOID:0060365
  • mandibulofacial dysostosis with alopecia
  • Aliases:
    • MFDA
Mus musculus (house mouse)
DOID:0111189
  • distal myopathy 3
  • Aliases:
    • MPD3
    • distal muscular dystrophy 3
    • distal myopathy type 3
Mus musculus (house mouse)
DOID:0110840
  • Usher syndrome type 2D
  • Aliases:
    • USH2D
    • Usher syndrome type IID
Drosophila melanogaster (fruit fly)
DOID:0110346
  • osteogenesis imperfecta type 10
  • Aliases:
    • OI10
    • osteogenesis imperfecta type X
Homo sapiens (human)
DOID:0112147
  • retinitis pigmentosa 90
  • Aliases:
    • RP90
Saccharomyces cerevisiae S288C
DOID:4306
  • radiculopathy
  • Aliases:
    • pinched nerve
Mus musculus (house mouse)
DOID:0110425
  • dilated cardiomyopathy 1A
  • Aliases:
    • CDCD1
    • dilated cardiomyopathy with conduction defect 1
    • familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Rattus norvegicus (Norway rat)
DOID:0110306
  • autosomal dominant limb-girdle muscular dystrophy type 3
  • Aliases:
    • LGMD1G
    • autosomal dominant limb-girdle muscular dystrophy type 1G
    • muscular dystrophy limb-girdle type 1G
Drosophila melanogaster (fruit fly)
DOID:2237
  • hepatitis
  • Aliases:
    • acute and subacute liver necrosis
    • acute hepatitis
    • acute/subac. necrosis of liver
    • animal hepatitis
    • chronic hepatitis
    • chronic persistent hepatitis
Saccharomyces cerevisiae S288C
DOID:0112314
  • brain small vessel disease 2
  • Aliases:
    • BSVD2
    • porencephaly 2
Mus musculus (house mouse)
DOID:0060685
  • autosomal dominant nocturnal frontal lobe epilepsy 4
  • Aliases:
    • ENFL4
    • nocturnal frontal lobe epilepsy 4
Rattus norvegicus (Norway rat)
DOID:0050580
  • hereditary lymphedema
Danio rerio (zebrafish)
DOID:0080205
  • CAKUT
  • Aliases:
    • Congenital anomalies of the kidney and urinary tract
    • Renal or urinary tract malformation
Drosophila melanogaster (fruit fly)
DOID:5410
  • pulmonary neuroendocrine tumor
Caenorhabditis elegans
DOID:0110698
  • hypotrichosis 1
  • Aliases:
    • Hhs
    • Hts
    • Hypt1
    • hereditary generalized hypotrichosis simplex
Homo sapiens (human)
DOID:0081229
  • autosomal recessive intellectual developmental disorder 68
Mus musculus (house mouse)
DOID:0050545
  • visceral heterotaxy
  • Aliases:
    • heterotaxia
    • situs ambiguus
Xenopus laevis (African clawed frog)
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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