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 4101 - 4125 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism
DOID:0080149
  • adult acute monocytic leukemia
Homo sapiens (human)
DOID:0111532
  • osteoglophonic dysplasia
  • Aliases:
    • Fairbank-Keats syndrome
    • OGD
    • osteoglophonic dwarfism
Homo sapiens (human)
DOID:2634
  • cystadenoma
  • Aliases:
    • Cystoma
Homo sapiens (human)
DOID:14291
  • Noonan syndrome with multiple lentigines
  • Aliases:
    • Capute-Rimoin-Konigsmark-Esterly-Richardson syndrome
    • Generalized lentiginosis
    • Gorlin syndrome II
    • LEOPARD syndrome
    • Lentiginosis profusa syndrome
    • Moynahan syndrome
    • Multiple lentigines syndrome
    • Progressive cardiomyopathic lentiginosis
Homo sapiens (human)
DOID:0080191
  • PTEN hamartoma tumor syndrome
Homo sapiens (human)
DOID:0080548
  • Noonan syndrome with multiple lentigines 1
  • Aliases:
    • LEOPARD syndrome 1
Homo sapiens (human)
DOID:3350
  • mesenchymal cell neoplasm
  • Aliases:
    • benign miscellaneous mesenchymal tumor
    • mesenchymal tumor
Homo sapiens (human)
DOID:4313
  • epidermolysis bullosa acquisita
  • Aliases:
    • acquired epidermolysis bullosa
Homo sapiens (human)
DOID:0080158
  • herpes simplex virus keratitis
  • Aliases:
    • dendritic keratitis
Homo sapiens (human)
DOID:3674
  • kidney rhabdoid cancer
  • Aliases:
    • renal Rhabdoid tumor
    • rhabdoid tumor of the kidney
Homo sapiens (human)
DOID:5160
  • arteriosclerosis obliterans
Homo sapiens (human)
DOID:11555
  • Fuchs' endothelial dystrophy
  • Aliases:
    • FCED
    • Fuchs' corneal dystrophy
    • Fuchs' endothelial corneal dystrophy
Homo sapiens (human)
DOID:11554
  • Chandler syndrome
  • Aliases:
    • Chandler's syndrome
    • Dystrophy of corneal endothelium
    • Endothelial corneal dystrophy
    • Posterior membrane corneal dystrophy
Homo sapiens (human)
DOID:0070314
  • obstructive nephropathy
  • Aliases:
    • CON
    • congenital obstructive nephropathy
Homo sapiens (human)
DOID:0111454
  • SHORT syndrome
  • Aliases:
    • Aarskog-Ose-Pande syndrome
    • Lipodystrophy-Rieger anomaly-diabetes syndrome
    • Rieger anomaly-partial lipodystrophy syndrome
    • short stature, hyperextensibility, hernia, ocular depression, Rieger anomaly, and teething delay
Homo sapiens (human)
DOID:0050765
  • neuroacanthocytosis
Homo sapiens (human)
DOID:0080521
  • lung non-squamous non-small cell carcinoma
  • Aliases:
    • non- squamous NSCLC
Homo sapiens (human)
DOID:0060463
  • NUT midline carcinoma
  • Aliases:
    • nuclear protein in testis midline carcinoma
Homo sapiens (human)
DOID:5692
  • cellular myxoid liposarcoma
  • Aliases:
    • Round cell liposarcoma
Homo sapiens (human)
DOID:12960
  • acrocephalosyndactylia
  • Aliases:
    • Apert syndrome
Homo sapiens (human)
DOID:5439
  • papillary hidradenoma
Homo sapiens (human)
DOID:5303
  • cervical clear cell adenocarcinoma
  • Aliases:
    • Clear cell carcinoma of the Cervix Uteri
Homo sapiens (human)
DOID:9181
  • amebiasis
  • Aliases:
    • amoebiasis
    • entamoebiasis
Homo sapiens (human)
DOID:14705
  • Pfeiffer syndrome
  • Aliases:
    • acrocephalosyndactylia type V
Homo sapiens (human)
DOID:14768
  • Saethre-Chotzen syndrome
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