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 6501 - 6525 of 7942 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism
DOID:0050161
  • lower respiratory tract disease
Homo sapiens (human)
DOID:4491
  • persian gulf syndrome
  • Aliases:
    • Gulf war syndrome
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: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:0111225
  • centronuclear myopathy X-linked
  • Aliases:
    • CNMX
    • MTM1
    • X-linked myotubular myopathy
    • XLCNM
    • XLMTM
    • myotubular myopathy 1
Homo sapiens (human)
DOID:2218
  • blood platelet disease
  • Aliases:
    • Thrombocytopathy
    • platelet disorder
Homo sapiens (human)
DOID:0080110
  • contractures, pterygia, and spondylocarpotarsal fusion syndrome
  • Aliases:
    • multiple pterygium syndrome
Homo sapiens (human)
DOID:439
  • neuromuscular junction disease
Homo sapiens (human)
DOID:654
  • overnutrition
Homo sapiens (human)
DOID:1148
  • polydactyly
  • Aliases:
    • postaxial polydactyly
Homo sapiens (human)
DOID:10112
  • sleeping sickness
  • Aliases:
    • African sleeping sickness
    • African trypanosomiasis
Homo sapiens (human)
DOID:2479
  • central nervous system origin vertigo
  • Aliases:
    • Vertigo of central origin
    • central vestibular vertigo
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:0060306
  • Meier-Gorlin syndrome
  • Aliases:
    • ear-patella-short stature syndrome
Homo sapiens (human)
DOID:0080512
  • Meier-Gorlin syndrome 1
Homo sapiens (human)
DOID:3534
  • Lafora disease
  • Aliases:
    • Lafora Progressive Myoclonic Epilepsy
    • Lafora's disease
    • MYOCLONIC EPILEPSY OF LAFORA
Homo sapiens (human)
DOID:0050214
  • Lambert-Eaton myasthenic syndrome
  • Aliases:
    • Eaton-Lambert syndrome
    • LEMS
    • Lambert-Eaton syndrome
Homo sapiens (human)
DOID:13481
  • thanatophoric dysplasia
Homo sapiens (human)
DOID:1192
  • peripheral nervous system neoplasm
  • Aliases:
    • neoplasm of peripheral nerve
    • nerve sheath neoplasm
    • tumor of PNS
Homo sapiens (human)
DOID:962
  • neurofibroma
Homo sapiens (human)
DOID:0080188
  • chronic myelomonocytic leukemia
Homo sapiens (human)
DOID:9470
  • bacterial meningitis
Homo sapiens (human)

About Release Notes Help Feedback

International Collaboration

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024