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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 1526 - 1550 of 5716 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism Source
DOID:0080312
  • neurodevelopmental disorder with midbrain and hindbrain malformations
  • Aliases:
    • NEDMHM
Homo sapiens (human)
DOID:0080313
  • cleft palate-lateral synechia syndrome
  • Aliases:
    • CPLS syndrome
    • syngnathia
Mus musculus (house mouse)
DOID:0080315
  • megalencephalic leukoencephalopathy with subcortical cysts
  • Aliases:
    • megalencephalic leukodystrophy megalencephaly-cystic leukodystorphy syndrome
    • vacuolating megalencephalic leukoencephalopathy with subcortical cysts
Homo sapiens (human)
DOID:0080315
  • megalencephalic leukoencephalopathy with subcortical cysts
  • Aliases:
    • megalencephalic leukodystrophy megalencephaly-cystic leukodystorphy syndrome
    • vacuolating megalencephalic leukoencephalopathy with subcortical cysts
Mus musculus (house mouse)
DOID:0080317
  • megalencephalic leukoencephalopathy with subcortical cysts 2B
  • Aliases:
    • megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without mental retardation
Homo sapiens (human)
DOID:0080318
  • megalencephalic leukoencephalopathy with subcortical cysts 2A
Homo sapiens (human)
DOID:0080319
  • X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia
  • Aliases:
    • XMEN
Homo sapiens (human)
DOID:0080322
  • polycystic kidney disease
Homo sapiens (human)
DOID:0080322
  • polycystic kidney disease
Danio rerio (zebrafish)
DOID:0080322
  • polycystic kidney disease
Rattus norvegicus (Norway rat)
DOID:0080322
  • polycystic kidney disease
Mus musculus (house mouse)
DOID:0080324
  • tuberous sclerosis 1
Homo sapiens (human)
DOID:0080325
  • tuberous sclerosis 2
Homo sapiens (human)
DOID:0080326
  • familial hypertrophic cardiomyopathy
Homo sapiens (human)
DOID:0080328
  • Culler-Jones syndrome
Homo sapiens (human)
DOID:0080329
  • cold-induced sweating syndrome 1
Homo sapiens (human)
DOID:0080330
  • cold-induced sweating syndrome 2
Homo sapiens (human)
DOID:0080331
  • cold-induced sweating syndrome 3
Homo sapiens (human)
DOID:0080333
  • aortic valve disease 1
Homo sapiens (human)
DOID:0080334
  • aortic valve disease 2
Homo sapiens (human)
DOID:0080336
  • mitochondrial DNA depletion syndrome 14
Homo sapiens (human)
DOID:0080337
  • mitochondrial DNA depletion syndrome 15
Homo sapiens (human)
DOID:0080339
  • familial erythrocytosis 4
  • Aliases:
    • ECYT4
Homo sapiens (human)
DOID:0080345
  • blepharocheilodontic syndrome 1
Homo sapiens (human)
DOID:0080346
  • blepharocheilodontic syndrome 2
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: December 8, 2025