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 1426 - 1450 of 7942 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism
DOID:0060306
  • Meier-Gorlin syndrome
  • Aliases:
    • ear-patella-short stature syndrome
Homo sapiens (human)
DOID:0050526
  • Gamstorp-Wohlfart syndrome
  • Aliases:
    • autosomal recessive neuromyotonia and axonal neuropathy
    • myokymia, myotonia and muscle wasting
Homo sapiens (human)
DOID:0050989
  • episodic ataxia type 1
Homo sapiens (human)
DOID:2479
  • central nervous system origin vertigo
  • Aliases:
    • Vertigo of central origin
    • central vestibular vertigo
Homo sapiens (human)
DOID:10112
  • sleeping sickness
  • Aliases:
    • African sleeping sickness
    • African trypanosomiasis
Homo sapiens (human)
DOID:1148
  • polydactyly
  • Aliases:
    • postaxial polydactyly
Homo sapiens (human)
DOID:654
  • overnutrition
Homo sapiens (human)
DOID:439
  • neuromuscular junction disease
Homo sapiens (human)
DOID:0080110
  • contractures, pterygia, and spondylocarpotarsal fusion syndrome
  • Aliases:
    • multiple pterygium syndrome
Homo sapiens (human)
DOID:2218
  • blood platelet disease
  • Aliases:
    • Thrombocytopathy
    • platelet disorder
Homo sapiens (human)
DOID:0111225
  • centronuclear myopathy X-linked
  • Aliases:
    • CNMX
    • MTM1
    • X-linked myotubular myopathy
    • XLCNM
    • XLMTM
    • myotubular myopathy 1
Homo sapiens (human)
DOID:4697
  • perineurioma
  • Aliases:
    • soft tissue Perineurioma
Homo sapiens (human)
DOID:3193
  • peripheral nerve sheath neoplasm
  • Aliases:
    • neoplasm of the nerve Sheath
    • nerve sheath tumour
Homo sapiens (human)
DOID:974
  • upper respiratory tract disease
Homo sapiens (human)
DOID:0110667
  • congenital myasthenic syndrome 5
  • Aliases:
    • CMS Ic
    • CMS5
    • EAD
    • Engel congenital myasthenic syndrome
    • congenital myasthenic syndrome Engel type
    • congenital myasthenic syndrome type Ic
    • end plate acetylcholinesterase deficiency
Homo sapiens (human)
DOID:0050161
  • lower respiratory tract disease
Homo sapiens (human)
DOID:4847
  • cauda equina neoplasm
  • Aliases:
    • tumor of the Cauda Equina
Homo sapiens (human)
DOID:0060814
  • Wilson-Turner syndrome
  • Aliases:
    • MRXS6
    • WTS
    • X-linked intellectual disability-gynecomastia-obesity syndrome
    • mental retardation, X-linked, syndromic 6
    • mental retardation, X-linked, with gynecomastia and obesity
Homo sapiens (human)
DOID:2163
  • nasal cavity disease
Homo sapiens (human)
DOID:3876
  • colonic pseudo-obstruction
  • Aliases:
    • primary chronic pseudo-obstruction of colon
Homo sapiens (human)
DOID:1352
  • paranasal sinus disease
  • Aliases:
    • disorder of nasal sinus
Homo sapiens (human)
DOID:6088
  • acute stress disorder
  • Aliases:
    • traumatic stress disorder
Homo sapiens (human)
DOID:4491
  • persian gulf syndrome
  • Aliases:
    • Gulf war syndrome
Homo sapiens (human)
DOID:3429
  • inclusion body myositis
Homo sapiens (human)
DOID:3910
  • lung adenocarcinoma
  • Aliases:
    • bronchogenic lung adenocarcinoma
    • nonsmall cell adenocarcinoma
Homo sapiens (human)

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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: August 19, 2024