GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources October 9, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 1501 - 1525 of 4649 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▲
DOID:0081144
  • common variable immunodeficiency 1
Homo sapiens (human)
DOID:0081145
  • common variable immunodeficiency 2
Homo sapiens (human)
DOID:0081146
  • common variable immunodeficiency 3
Homo sapiens (human)
DOID:0081147
  • common variable immunodeficiency 4
Homo sapiens (human)
DOID:0081148
  • common variable immunodeficiency 5
Homo sapiens (human)
DOID:0081150
  • common variable immunodeficiency 7
Homo sapiens (human)
DOID:0081151
  • common variable immunodeficiency 8
  • Aliases:
    • common variable immunodeficiency-8 (CVID8) with autoimmunity
Homo sapiens (human)
DOID:0081152
  • common variable immunodeficiency 10
Homo sapiens (human)
DOID:0081153
  • common variable immunodeficiency 11
Homo sapiens (human)
DOID:0081154
  • common variable immunodeficiency 12
Homo sapiens (human)
DOID:0081155
  • common variable immunodeficiency 13
Homo sapiens (human)
DOID:0081156
  • common variable immunodeficiency 14
Homo sapiens (human)
DOID:0081157
  • dilated cardiomyopathy 1LL
Homo sapiens (human)
DOID:0081158
  • dilated cardiomyopathy 1MM
Homo sapiens (human)
DOID:0081163
  • dilated cardiomyopathy 2G
Homo sapiens (human)
DOID:0081164
  • dilated cardiomyopathy 3B
Homo sapiens (human)
DOID:0081168
  • HMG-CoA synthase 2 deficiency
  • Aliases:
    • 3-hydroxy-3-methylglutaryl-CoA synthase-2 deficiency
Homo sapiens (human)
DOID:0081175
  • short stature, hearing loss, retinitis pigmentosa, and distinctive facies
Homo sapiens (human)
DOID:0081177
  • autosomal recessive intellectual developmental disorder 1
Homo sapiens (human)
DOID:0081179
  • autosomal recessive intellectual developmental disorder 3
Homo sapiens (human)
DOID:0081181
  • autosomal recessive intellectual developmental disorder 5
Homo sapiens (human)
DOID:0081182
  • autosomal recessive intellectual developmental disorder 6
Homo sapiens (human)
DOID:0081188
  • autosomal recessive intellectual developmental disorder 14
Homo sapiens (human)
DOID:0081190
  • autosomal recessive intellectual developmental disorder 18
Homo sapiens (human)
DOID:0081202
  • autosomal recessive intellectual developmental disorder 37
Homo sapiens (human)

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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: December 9, 2024