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 926 - 950 of 4621 in total
Disease ID Disease Name ▲ Gene Symbol Gene ID Organism
DOID:57
  • aortic valve insufficiency
  • Aliases:
    • Rheumatic aortic insufficiency
    • Rheumatic aortic regurgitation
    • Rheumatic aortic valve regurgitation
    • aortic incompetence
    • aortic insufficiency
    • aortic regurgitation
    • rheumatic aortic valve insufficiency
Homo sapiens (human)
DOID:1712
  • aortic valve stenosis
  • Aliases:
    • Aortic stenosis
    • Rheumatic aortic stenosis
    • rheumatic aortic valve stenosis
Homo sapiens (human)
DOID:519
  • aortitis
Homo sapiens (human)
DOID:0060046
  • aphasia
Homo sapiens (human)
DOID:9663
  • aphthous stomatitis
  • Aliases:
    • Aphtha
    • Aphthous ulceration
    • Canker sore
    • Oral aphthae
    • oral ulcer
Homo sapiens (human)
DOID:12449
  • aplastic anemia
Homo sapiens (human)
DOID:3895
  • apocrine adenoma
  • Aliases:
    • tubular Apocrine adenoma
Homo sapiens (human)
DOID:4367
  • apparent mineralocorticoid excess syndrome
  • Aliases:
    • 11-beta-hydroxysteroid dehydrogenase deficiency type 2
    • Ulick syndrome
    • cortisol 11-beta-ketoreductase deficiency
    • syndrome of apparent mineralocorticoid excess
Homo sapiens (human)
DOID:8337
  • appendicitis
  • Aliases:
    • acute appendicitis
    • acute appendicitis with generalized peritonitis
    • acute appendicitis with peritoneal abscess
Homo sapiens (human)
DOID:0060135
  • apraxia
Homo sapiens (human)
DOID:12156
  • arachnoiditis
Homo sapiens (human)
DOID:11342
  • arcus senilis
  • Aliases:
    • Arcus of cornea
    • corneal arcus
Homo sapiens (human)
DOID:14755
  • argininosuccinic aciduria
  • Aliases:
    • Argininosuccinate lyase deficiency
    • argininosuccinic acidemia
    • arginosuccinase deficiency
    • deficiency of argininosuccinate lyase
Homo sapiens (human)
DOID:0090122
  • aromatase excess syndrome
  • Aliases:
    • AEXS
    • familial hyperestrogenism
    • hereditary prepubertal gynecomastia
    • increased aromatase activity
Homo sapiens (human)
DOID:0050431
  • arrhythmogenic right ventricular cardiomyopathy
  • Aliases:
    • ARVC
    • ARVC cardiomyopathy
    • ARVD
    • arrhythmogenic right ventricular dysplasia
    • arrhythmogenic right ventricular dysplasia/cardiomyopathy
    • right ventricular ACM
Homo sapiens (human)
DOID:0050644
  • arterial calcification of infancy
  • Aliases:
    • generalized arterial calcification of infancy
    • idiopathic infantile arterial calcification
    • infantile arteriosclerosis
Homo sapiens (human)
DOID:0050645
  • arterial tortuosity syndrome
Homo sapiens (human)
DOID:5162
  • arteriolosclerosis
Homo sapiens (human)
DOID:5160
  • arteriosclerosis obliterans
Homo sapiens (human)
DOID:2349
  • arteriosclerosis
  • Aliases:
    • Arteriosclerotic vascular disease
Homo sapiens (human)
DOID:2348
  • arteriosclerotic cardiovascular disease
  • Aliases:
    • Cardiovascular arteriosclerosis
Homo sapiens (human)
DOID:11294
  • arteriovenous malformation
  • Aliases:
    • Arteriovenous hemangioma
    • Cirsoid aneurysm
    • Racemose Angioma
    • Racemose aneurysm
    • Racemose hemangioma
Homo sapiens (human)
DOID:0060688
  • arteriovenous malformations of the brain
  • Aliases:
    • cerebral arteriovenous malformation
    • intracranial arteriovenous malformation
Homo sapiens (human)
DOID:848
  • arthritis
  • Aliases:
    • Inflammatory disorder of joint
Homo sapiens (human)
DOID:0111353
  • arthrogryposis, renal dysfunction, and cholestasis 1
  • Aliases:
    • ARCS1
Homo sapiens (human)

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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


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Last updated: August 19, 2024