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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 January 28, 2025
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 1501 - 1525 of 5716 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism Source
DOID:0080266
  • primary ciliary dyskinesia 37
Homo sapiens (human)
DOID:0080267
  • autosomal dominant nonsyndromic deafness 71
Homo sapiens (human)
DOID:0080268
  • autosomal dominant nonsyndromic deafness 72
Homo sapiens (human)
DOID:0080272
  • nephrotic syndrome type 16
Homo sapiens (human)
DOID:0080280
  • gingival fibromatosis 5
Homo sapiens (human)
DOID:0080281
  • schizophrenia 19
Homo sapiens (human)
DOID:0080282
  • developmental and epileptic encephalopathy 56
  • Aliases:
    • DEE56
    • early infantile epileptic encephalopathy 56
Homo sapiens (human)
DOID:0080283
  • developmental and epileptic encephalopathy 55
  • Aliases:
    • DEE55
    • GPIBD14
    • early infantile epileptic encephalopathy 55
    • glycosylphosphatidylinositol biosynthesis defect 14
Homo sapiens (human)
DOID:0080284
  • developmental and epileptic encephalopathy 57
  • Aliases:
    • DEE57
    • early infantile epileptic encephalopathy 57
Homo sapiens (human)
DOID:0080285
  • developmental and epileptic encephalopathy 58
  • Aliases:
    • DEE58
    • early infantile epileptic encephalopathy 58
Homo sapiens (human)
DOID:0080286
  • spinocerebellar ataxia 44
Homo sapiens (human)
DOID:0080287
  • spinocerebellar ataxia 45
Homo sapiens (human)
DOID:0080288
  • spinocerebellar ataxia 46
Homo sapiens (human)
DOID:0080289
  • orofaciodigital syndrome XVII
Homo sapiens (human)
DOID:0080290
  • familial erythrocytosis 5
  • Aliases:
    • ECYT5
Homo sapiens (human)
DOID:0080291
  • developmental and epileptic encephalopathy 59
  • Aliases:
    • DEE59
    • early infantile epileptic encephalopathy 59
Homo sapiens (human)
DOID:0080294
  • Charcot-Marie-Tooth disease dominant intermediate G
Homo sapiens (human)
DOID:0080297
  • Coffin-Siris syndrome 6
Homo sapiens (human)
DOID:0080299
  • partial lipodystrophy
Homo sapiens (human)
DOID:0080301
  • atypical hemolytic-uremic syndrome
Homo sapiens (human)
DOID:0080301
  • atypical hemolytic-uremic syndrome
Mus musculus (house mouse)
DOID:0080308
  • myofibrillar myopathy 8
Homo sapiens (human)
DOID:0080309
  • fatal infantile hypertonic myofibrillar myopathy
Homo sapiens (human)
DOID:0080311
  • X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance
Homo sapiens (human)
DOID:0080312
  • neurodevelopmental disorder with midbrain and hindbrain malformations
  • Aliases:
    • NEDMHM
Mus musculus (house mouse)
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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: April 6, 2026