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 6001 - 6025 of 7942 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism
DOID:0060695
  • hyperekplexia
  • Aliases:
    • Kok disease
    • congenital stiff man syndrome
    • familial startle disease
    • hereditary hyperekplexia
    • startle disease
Homo sapiens (human)
DOID:5434
  • scrapie
Homo sapiens (human)
DOID:648
  • kuru
  • Aliases:
    • kuru encephalopathy
Homo sapiens (human)
DOID:0060696
  • hyperekplexia 1
  • Aliases:
    • HKPX1
Homo sapiens (human)
DOID:12171
  • radial neuropathy
Homo sapiens (human)
DOID:0060697
  • hyperekplexia 2
  • Aliases:
    • HKPX2
Homo sapiens (human)
DOID:12170
  • radial nerve lesion
  • Aliases:
    • Lesion of radial nerve
    • Radial nerve lesions
Homo sapiens (human)
DOID:0050980
  • spinocerebellar ataxia type 31
Homo sapiens (human)
DOID:14070
  • vestibular nystagmus
  • Aliases:
    • Nystagmus associated with disorder of the vestibular system
Homo sapiens (human)
DOID:3530
  • chronic wasting disease
Homo sapiens (human)
DOID:0060698
  • hyperekplexia 3
  • Aliases:
    • HKPX3
Homo sapiens (human)
DOID:4267
  • akinetic mutism
  • Aliases:
    • Coma vigilans
Homo sapiens (human)
DOID:1442
  • obsolete Alpers syndrome
Homo sapiens (human)
DOID:0080122
  • Alpers-Huttenlocher syndrome
  • Aliases:
    • Alper's syndrome
    • Alpers disease
    • Alpers progressive infantile poliodystrophy
    • Alpers syndrome
    • Alpers' disease or gray-matter degeneration
    • Diffuse Cerebral Sclerosis of Schilder
    • mitochondrial DNA depletion syndrome 4a
    • progressive sclerosing poliodystrophy
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:0111739
  • X-linked deafness 1
  • Aliases:
    • DFN2
    • DFNX1
    • X-linked sensorineural congenital deafness 2
Homo sapiens (human)
DOID:0080161
  • cutaneous candidiasis
Homo sapiens (human)
DOID:10242
  • ehrlichiosis
  • Aliases:
    • human ehrlichiosis
Homo sapiens (human)
DOID:0111507
  • Lenz-Majewski hyperostotic dwarfism
  • Aliases:
    • Lenz-Majewski syndrome
Homo sapiens (human)
DOID:12273
  • anisometropia
Homo sapiens (human)
DOID:5151
  • plexiform neurofibroma
Homo sapiens (human)
DOID:12732
  • intermediate uveitis
  • Aliases:
    • chronic cyclitis
    • peripheral uveoretinitis
Homo sapiens (human)
DOID:7614
  • meninges sarcoma
  • Aliases:
    • Meningeal sarcoma
    • sarcoma of meninges
Homo sapiens (human)
DOID:3001
  • female reproductive endometrioid cancer
  • Aliases:
    • endometrioid neoplasm
    • endometrioid tumor
Homo sapiens (human)

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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