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 2401 - 2425 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼
DOID:0060291
  • oculodentodigital dysplasia
  • Aliases:
    • ODD syndrome
Homo sapiens (human)
DOID:1415
  • gyrate atrophy
  • Aliases:
    • Gyrate atrophy of the choroid and/or retina
    • Ornithinemia with gyrate atrophy
    • gyrate atrophy of the retina
Homo sapiens (human)
DOID:0050242
  • primary amebic meningoencephalitis
  • Aliases:
    • Naegleria fowleri infection
Homo sapiens (human)
DOID:0110136
  • Bardet-Biedl syndrome 14
  • Aliases:
    • BBS14
Homo sapiens (human)
DOID:11934
  • head and neck cancer
  • Aliases:
    • head and neck neoplasm
    • head and neck tumours
    • head/neck neoplasm
    • tumor of head and neck
Homo sapiens (human)
DOID:5692
  • cellular myxoid liposarcoma
  • Aliases:
    • Round cell liposarcoma
Homo sapiens (human)
DOID:1166
  • palindromic rheumatism
  • Aliases:
    • Hench's syndrome
    • Hench-Rosenberg syndrome
Homo sapiens (human)
DOID:1564
  • fungal infectious disease
  • Aliases:
    • mycosis
Homo sapiens (human)
DOID:3878
  • obsolete intestinal pseudo-obstruction
Homo sapiens (human)
DOID:12528
  • lesion of sciatic nerve
Homo sapiens (human)
DOID:5672
  • large intestine cancer
Homo sapiens (human)
DOID:3389
  • Papillon-Lefevre disease
  • Aliases:
    • Papillon Lefevre syndrome
    • Papillon-Lefvre syndrome
Homo sapiens (human)
DOID:6929
  • retinal edema
Homo sapiens (human)
DOID:0080491
  • cerebral cavernous malformation 1
Homo sapiens (human)
DOID:0111527
  • spinal muscular atrophy with progressive myoclonic epilepsy
  • Aliases:
    • Jankovic-Rivera syndrome
    • SMA-PME
    • SMAPME
    • hereditary myoclonus-progressive distal muscular atrophy syndrome
Homo sapiens (human)
DOID:5662
  • pleomorphic carcinoma
Homo sapiens (human)
DOID:0060346
  • Native American myopathy
  • Aliases:
    • Bailey-Bloch congenital myopathy
    • congenital myopathy 13
Homo sapiens (human)
DOID:0110158
  • Charcot-Marie-Tooth disease type 2I
  • Aliases:
    • CMT2I
    • Charcot-Marie-Tooth neuropathy type 2I
Homo sapiens (human)
DOID:0050535
  • exudative vitreoretinopathy
  • Aliases:
    • FEVR
    • familial exudative vitreoretinopathy
Homo sapiens (human)
DOID:1443
  • cerebral degeneration
  • Aliases:
    • Brain degeneration
Homo sapiens (human)
DOID:0110492
  • autosomal recessive nonsyndromic deafness 33
  • Aliases:
    • DFNB33
    • autosomal recessive deafness 33
Homo sapiens (human)
DOID:0110881
  • holoprosencephaly 1
  • Aliases:
    • HPE1
Homo sapiens (human)
DOID:3590
  • gestational trophoblastic neoplasm
  • Aliases:
    • gestational trophoblastic neoplasia
    • hydatidiform mole
    • molar pregnancy
Homo sapiens (human)
DOID:0110843
  • xeroderma pigmentosum group A
  • Aliases:
    • XP group A
    • XP1
    • XPA
    • xeroderma pigmentosum 1
    • xeroderma pigmentosum complementation group A
Homo sapiens (human)
DOID:854
  • collagen disease
  • Aliases:
    • collagen disorder
Homo sapiens (human)

About Release Notes Help Feedback

Click here to visit the beta site.


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