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 4676 - 4700 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼
DOID:0110589
  • autosomal dominant nonsyndromic deafness 68
  • Aliases:
    • DFNA68
    • autosomal dominant deafness 68
Homo sapiens (human)
DOID:823
  • periapical periodontitis
  • Aliases:
    • Apical periodontitis
Homo sapiens (human)
DOID:0110567
  • autosomal dominant nonsyndromic deafness 41
  • Aliases:
    • DFNA41
    • autosomal dominant deafness 41
Homo sapiens (human)
DOID:672
  • spleen cancer
  • Aliases:
    • Splenic neoplasm
    • malignant Splenic tumor
    • malignant tumour of spleen
    • spleen neoplasm
Homo sapiens (human)
DOID:0110206
  • Charcot-Marie-Tooth disease dominant intermediate F
  • Aliases:
    • CMTDIF
    • autosomal dominant intermediate Charcot-Marie-Tooth disease type F
Homo sapiens (human)
DOID:0111420
  • familial GPIHBP1 deficiency
  • Aliases:
    • familial glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein 1 deficiency
    • hyperlipoproteinemia type 1D
    • hyperlipoproteinemia type ID
Homo sapiens (human)
DOID:4176
  • blood group incompatibility
Homo sapiens (human)
DOID:7848
  • interdigitating dendritic cell sarcoma
  • Aliases:
    • Interdigitating cell sarcoma
Homo sapiens (human)
DOID:0080071
  • mucolipidosis III alpha/beta
  • Aliases:
    • mucolipidosis III
    • pseudo-Hurler polydystrophy
Homo sapiens (human)
DOID:0050466
  • Loeys-Dietz syndrome
Homo sapiens (human)
DOID:14555
  • Foster-Kennedy syndrome
Homo sapiens (human)
DOID:0050729
  • Chanarin-Dorfman syndrome
  • Aliases:
    • neutral lipid storage disease
Homo sapiens (human)
DOID:0111353
  • arthrogryposis, renal dysfunction, and cholestasis 1
  • Aliases:
    • ARCS1
Homo sapiens (human)
DOID:12273
  • anisometropia
Homo sapiens (human)
DOID:11840
  • coronary artery vasospasm
  • Aliases:
    • Coronary Vasospasm
    • Coronary artery spasm
Homo sapiens (human)
DOID:3737
  • verrucous carcinoma
  • Aliases:
    • Warty carcinoma
    • verrucous squamous carcinoma
    • verrucous squamous cell carcinoma
Homo sapiens (human)
DOID:5505
  • papillary ependymoma
Homo sapiens (human)
DOID:2785
  • Dandy-Walker syndrome
  • Aliases:
    • Atresia of foramina of Magendie and Luschka
Homo sapiens (human)
DOID:0110261
  • cataract 35
  • Aliases:
    • CATCN1
    • CTRCT35
    • autosomal recessive congenital nuclear cataract 1
    • cataract 35, congenital nuclear
Homo sapiens (human)
DOID:12157
  • aseptic meningitis
  • Aliases:
    • acute aseptic meningitis
Homo sapiens (human)
DOID:10286
  • prostate carcinoma
  • Aliases:
    • cancer of prostate
    • carcinoma of prostate
Homo sapiens (human)
DOID:6419
  • tetralogy of Fallot
  • Aliases:
    • Ventricular septal defect with pulmonary stenosis or atresia, dextraposition of aorta, and hypertrophy of right ventricle
Homo sapiens (human)
DOID:0060588
  • Noonan syndrome 10
  • Aliases:
    • NS10
Homo sapiens (human)
DOID:1088
  • meningocele
Homo sapiens (human)
DOID:1682
  • congenital heart disease
  • Aliases:
    • Congenital Heart Defects
    • Congenital anomaly of heart
    • Heart Malformation
    • congenital heart defect
    • heart defect
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