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 1601 - 1625 of 4649 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism Source
DOID:0081210
  • autosomal recessive intellectual developmental disorder 46
Homo sapiens (human)
DOID:0081212
  • autosomal recessive intellectual developmental disorder 48
Homo sapiens (human)
DOID:0081213
  • autosomal recessive intellectual developmental disorder 50
Homo sapiens (human)
DOID:0081215
  • autosomal recessive intellectual developmental disorder 52
Homo sapiens (human)
DOID:0081216
  • autosomal recessive intellectual developmental disorder 54
Homo sapiens (human)
DOID:0081217
  • autosomal recessive intellectual developmental disorder 56
Homo sapiens (human)
DOID:0081218
  • autosomal recessive intellectual developmental disorder 74
Homo sapiens (human)
DOID:0081219
  • autosomal recessive intellectual developmental disorder 57
Homo sapiens (human)
DOID:0081220
  • autosomal recessive intellectual developmental disorder 58
Homo sapiens (human)
DOID:0081221
  • autosomal recessive intellectual developmental disorder 59
Homo sapiens (human)
DOID:0081223
  • glycosylphosphatidylinositol biosynthesis defect 16
  • Aliases:
    • Intellectual developmental disorder, autosomal recessive 62
Homo sapiens (human)
DOID:0081224
  • autosomal recessive intellectual developmental disorder 63
Homo sapiens (human)
DOID:0081225
  • autosomal recessive intellectual developmental disorder 64
Homo sapiens (human)
DOID:0081226
  • autosomal recessive intellectual developmental disorder 65
Homo sapiens (human)
DOID:0081228
  • autosomal recessive intellectual developmental disorder 67
Homo sapiens (human)
DOID:0081230
  • autosomal recessive intellectual developmental disorder 69
Homo sapiens (human)
DOID:0081231
  • autosomal recessive intellectual developmental disorder 70
Homo sapiens (human)
DOID:0081234
  • autosomal recessive intellectual developmental disorder 75
Homo sapiens (human)
DOID:0081235
  • autosomal recessive intellectual developmental disorder 76
Homo sapiens (human)
DOID:0081236
  • autosomal recessive intellectual developmental disorder 77
Homo sapiens (human)
DOID:0081237
  • acromesomelic dysplasia-3
  • Aliases:
    • Demirhan-type acromesomelic dysplasia
Homo sapiens (human)
DOID:0081242
  • autoimmune interstitial lung, joint, and kidney disease
  • Aliases:
    • Autoimmune interstitial lung disease-arthritis syndrome
    • COPA syndrome
Homo sapiens (human)
DOID:0081243
  • rhizomelic chondrodysplasia punctate type 4
Homo sapiens (human)
DOID:0081262
  • intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies
Homo sapiens (human)
DOID:0081263
  • neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities
  • Aliases:
    • NEDMCR syndrome
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: December 9, 2024