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 6676 - 6700 of 7942 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism
DOID:10780
  • primary polycythemia
  • Aliases:
    • Familiar Polycythemia
    • familial erythrocytosis
Homo sapiens (human)
DOID:0080033
  • craniometaphyseal dysplasia
Homo sapiens (human)
DOID:4331
  • burning mouth syndrome
  • Aliases:
    • Orodynia
    • Stomatopyrosis
Homo sapiens (human)
DOID:4483
  • rhinitis
Homo sapiens (human)
DOID:10310
  • viral meningitis
Homo sapiens (human)
DOID:1273
  • respiratory syncytial virus infectious disease
  • Aliases:
    • RSV
    • respiratory syncytial virus
Homo sapiens (human)
DOID:0050662
  • bestrophinopathy
  • Aliases:
    • autosomal recessive bestrophinopathy
Homo sapiens (human)
DOID:0110916
  • hereditary spherocytosis type 1
  • Aliases:
    • HS1
    • SPH1
    • hereditary spherocytosis 1
Homo sapiens (human)
DOID:5855
  • anteroseptal myocardial infarction
Homo sapiens (human)
DOID:5845
  • anterolateral myocardial infarction
Homo sapiens (human)
DOID:13025
  • retinopathy of prematurity
  • Aliases:
    • Retrolental fibroplasia
    • premature retinopathy
Homo sapiens (human)
DOID:0111412
  • exudative vitreoretinopathy 1
  • Aliases:
    • EVR1
Homo sapiens (human)
DOID:2388
  • renal artery disease
  • Aliases:
    • renal vascular disease
    • vascular disorder of kidney
Homo sapiens (human)
DOID:12783
  • migraine without aura
  • Aliases:
    • common migraine
Homo sapiens (human)
DOID:3240
  • aspiration pneumonitis
  • Aliases:
    • Chemical pneumonitis
    • Mendelson's Syndrome
Homo sapiens (human)
DOID:0050152
  • aspiration pneumonia
Homo sapiens (human)
DOID:12971
  • hereditary spherocytosis
  • Aliases:
    • Congenital spherocytic hemolytic anemia
    • Minkowski Chauffard syndrome
    • spherocytic anemia
Homo sapiens (human)
DOID:9719
  • neovascular inflammatory vitreoretinopathy
  • Aliases:
    • ADNIV
    • Retinitis proliferans
    • autosomal dominant neovascular inflammatory vitreoretinopathy
    • proliferative vitreoretinopathy
Homo sapiens (human)
DOID:2733
  • skin atrophy
  • Aliases:
    • Atrophoderma
    • Atrophy - skin
    • atrophic condition of skin
Homo sapiens (human)
DOID:0060444
  • granular corneal dystrophy 2
  • Aliases:
    • CGD2
    • avellino corneal dystrophy
    • combined granular-lattice corneal dystrophy
    • corneal dystrophy, Avellino type
    • granular corneal dystrophy type 2
Homo sapiens (human)
DOID:9182
  • pemphigus
Homo sapiens (human)
DOID:13404
  • uveoparotid fever
  • Aliases:
    • Heerfordt's syndrome
Homo sapiens (human)
DOID:1754
  • mitral valve stenosis
  • Aliases:
    • Mitral stenosis
Homo sapiens (human)
DOID:10272
  • left bundle branch hemiblock
  • Aliases:
    • Left bundle branch block
Homo sapiens (human)
DOID:1742
  • drug psychosis
  • Aliases:
    • Drug-induced psychosis
    • Drug-induced psychotic 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