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 126 - 150 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼
DOID:0050807
  • Kahrizi syndrome
  • Aliases:
    • KHRZ
    • intellectual disability, Kahrizi type
    • intellectual disability-cataract-coloboma-kyphosis syndrome
Homo sapiens (human)
DOID:0111865
  • MEND syndrome
  • Aliases:
    • male EBP disorder with neurological defects
Homo sapiens (human)
DOID:9810
  • polyarteritis nodosa
Homo sapiens (human)
DOID:11342
  • arcus senilis
  • Aliases:
    • Arcus of cornea
    • corneal arcus
Homo sapiens (human)
DOID:0080187
  • chronic neutrophilic leukemia
Homo sapiens (human)
DOID:2626
  • choroid plexus papilloma
  • Aliases:
    • childhood choroid plexus papilloma
Homo sapiens (human)
DOID:11759
  • hypochromic anemia
  • Aliases:
    • ANEMIA HYPOCHROMIC
Homo sapiens (human)
DOID:6000
  • congestive heart failure
  • Aliases:
    • CHF
    • Cardiac Failure Congestive
    • Congestive heart disease
    • Weak heart
Homo sapiens (human)
DOID:10485
  • esophageal atresia
  • Aliases:
    • Congenital atresia of esophagus
    • Congenital imperforate esophagus
    • Imperforate esophagus
    • Oesophageal atresia
Homo sapiens (human)
DOID:1510
  • personality disorder
  • Aliases:
    • character disorder
Homo sapiens (human)
DOID:4184
  • pseudohypoparathyroidism
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:3362
  • coronary aneurysm
  • Aliases:
    • Aneurysm of coronary vessels
    • Aneurysmal lesion of coronary artery
    • Arteriovenous aneurysm of coronary vessels
Homo sapiens (human)
DOID:12971
  • hereditary spherocytosis
  • Aliases:
    • Congenital spherocytic hemolytic anemia
    • Minkowski Chauffard syndrome
    • spherocytic anemia
Homo sapiens (human)
DOID:4817
  • ganglioneuroma
Homo sapiens (human)
DOID:4890
  • juvenile myoclonic epilepsy
Homo sapiens (human)
DOID:9801
  • tuberculous peritonitis
Homo sapiens (human)
DOID:14693
  • Clouston syndrome
  • Aliases:
    • Clouston's hidrotic ectodermal dysplasia
    • Clouston's syndrome
    • Hidrotic ectodermal dysplasia syndrome
    • ectodermal dysplasia 2, Clouston type
    • hidrotic ectodermal dysplasia
Homo sapiens (human)
DOID:698
  • dentin sensitivity
  • Aliases:
    • Sensitive dentin
Homo sapiens (human)
DOID:990
  • congenital heart block
Homo sapiens (human)
DOID:0060679
  • catecholaminergic polymorphic ventricular tachycardia 5
  • Aliases:
    • CVPT5
Homo sapiens (human)
DOID:1272
  • telangiectasis
  • Aliases:
    • telangiectasia
Homo sapiens (human)
DOID:0080342
  • Simpson-Golabi-Behmel syndrome type 2
Homo sapiens (human)
DOID:2799
  • bronchiolitis obliterans
  • Aliases:
    • Bronchiolitis exudativa
    • Bronchiolitis fibrosa obliterans
    • Obliterative bronchiolitis
Homo sapiens (human)
DOID:0110008
  • achromatopsia 3
  • Aliases:
    • ACHM1
    • ACHM3
    • Pingelapese blindness
    • RMCH1
    • rod monochromacy 1
    • rod monochromatism 1
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