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 851 - 875 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism
DOID:0112315
  • brain small vessel disease 3
  • Aliases:
    • BSVD3
Danio rerio (zebrafish)
DOID:784
  • chronic kidney disease
  • Aliases:
    • CKD
    • CRF
    • chronic kidney failure
    • chronic renal disease
    • chronic renal failure syndrome
    • renal failure - chronic
Danio rerio (zebrafish)
DOID:10787
  • premature menopause
  • Aliases:
    • Menopause - premature
    • Menopause praecox
Danio rerio (zebrafish)
DOID:0080208
  • metabolic dysfunction-associated steatotic liver disease
  • Aliases:
    • MAFLD
    • MASLD
    • NAFLD
    • metabolic dysfunction-associated fatty liver disease
    • metabolic dysfunction-related steatotic liver disease
    • metabolic-associated fatty liver disease
    • non-alcoholic fatty liver disease
    • nonalcoholic fatty liver disease
Danio rerio (zebrafish)
DOID:0060575
  • 3MC syndrome 1
Homo sapiens (human)
DOID:0060576
  • 3MC syndrome 2
Homo sapiens (human)
DOID:0050589
  • inflammatory bowel disease
Danio rerio (zebrafish)
DOID:0080201
  • Peters plus syndrome
  • Aliases:
    • Krause-Kivlin syndrome
    • Peters anomaly-short limb dwarfism syndrome
    • Peters-plus syndrome
Danio rerio (zebrafish)
DOID:0111240
  • congenital muscular dystrophy-dystroglycanopathy type A2
  • Aliases:
    • MDDGA2
    • Walker-Warburg syndrome or muscle-eye-brain disease, POMT2-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A2
Danio rerio (zebrafish)
DOID:0112380
  • muscular dystrophy-dystroglycanopathy type B2
  • Aliases:
    • MDDGB2
    • congenital muscular dystrophy POMT2-related
Danio rerio (zebrafish)
DOID:0110298
  • autosomal recessive limb-girdle muscular dystrophy type 2N
  • Aliases:
    • LGMD2N
    • muscular dystrophy-dystroglycanopathy (limb-girdle) type C 2
    • muscular dystrophy-dystroglycanopathy limb-girdle POMT2-related
Danio rerio (zebrafish)
DOID:0110274
  • autosomal recessive limb-girdle muscular dystrophy
Danio rerio (zebrafish)
DOID:0112374
  • muscular dystrophy-dystroglycanopathy
  • Aliases:
    • MDDG
Danio rerio (zebrafish)
DOID:0050453
  • lissencephaly
Danio rerio (zebrafish)
DOID:3181
  • oligodendroglioma
  • Aliases:
    • oligodendroglial neoplasm
    • oligodendroglial tumor
Mus musculus (house mouse)
DOID:0080322
  • polycystic kidney disease
Danio rerio (zebrafish)
DOID:0111739
  • X-linked deafness 1
  • Aliases:
    • DFN2
    • DFNX1
    • X-linked sensorineural congenital deafness 2
Homo sapiens (human)
DOID:0050647
  • Arts syndrome
  • Aliases:
    • ARTS
    • Lethal ataxia with deafness and optic atrophy
    • MRXS18
    • MRXSARTS
    • fatal X-linked ataxia with deafness and loss of vision
    • syndromic X-linked mental retardation 18
    • syndromic X-linked mental retardation Arts type
Homo sapiens (human)
DOID:0050542
  • Charcot-Marie-Tooth disease type X
Homo sapiens (human)
DOID:0110370
  • retinitis pigmentosa 55
  • Aliases:
    • RP55
Mus musculus (house mouse)
DOID:0060340
  • ciliopathy
Mus musculus (house mouse)
DOID:1935
  • Bardet-Biedl syndrome
Mus musculus (house mouse)
DOID:0110123
  • Bardet-Biedl syndrome 1
  • Aliases:
    • BBS1
Mus musculus (house mouse)
DOID:0110125
  • Bardet-Biedl syndrome 3
  • Aliases:
    • BBS3
Mus musculus (house mouse)
DOID:12171
  • radial neuropathy
Homo sapiens (human)

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

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