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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 October 9, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 12276 - 12300 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▼
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:0080315
  • megalencephalic leukoencephalopathy with subcortical cysts
  • Aliases:
    • megalencephalic leukodystrophy megalencephaly-cystic leukodystorphy syndrome
    • vacuolating megalencephalic leukoencephalopathy with subcortical cysts
Rattus norvegicus (Norway rat)
DOID:0080313
  • cleft palate-lateral synechia syndrome
  • Aliases:
    • CPLS syndrome
    • syngnathia
Caenorhabditis elegans
DOID:0080313
  • cleft palate-lateral synechia syndrome
  • Aliases:
    • CPLS syndrome
    • syngnathia
Homo sapiens (human)
DOID:0080313
  • cleft palate-lateral synechia syndrome
  • Aliases:
    • CPLS syndrome
    • syngnathia
Drosophila melanogaster (fruit fly)
DOID:0080313
  • cleft palate-lateral synechia syndrome
  • Aliases:
    • CPLS syndrome
    • syngnathia
Mus musculus (house mouse)
DOID:0080312
  • neurodevelopmental disorder with midbrain and hindbrain malformations
  • Aliases:
    • NEDMHM
Mus musculus (house mouse)
DOID:0080312
  • neurodevelopmental disorder with midbrain and hindbrain malformations
  • Aliases:
    • NEDMHM
Homo sapiens (human)
DOID:0080311
  • X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance
Mus musculus (house mouse)
DOID:0080311
  • X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance
Homo sapiens (human)
DOID:0080309
  • fatal infantile hypertonic myofibrillar myopathy
Mus musculus (house mouse)
DOID:0080309
  • fatal infantile hypertonic myofibrillar myopathy
Homo sapiens (human)
DOID:0080309
  • fatal infantile hypertonic myofibrillar myopathy
Rattus norvegicus (Norway rat)
DOID:0080301
  • atypical hemolytic-uremic syndrome
Rattus norvegicus (Norway rat)
DOID:0080301
  • atypical hemolytic-uremic syndrome
Caenorhabditis elegans
DOID:0080301
  • atypical hemolytic-uremic syndrome
Homo sapiens (human)
DOID:0080301
  • atypical hemolytic-uremic syndrome
Mus musculus (house mouse)
DOID:0080299
  • partial lipodystrophy
Mus musculus (house mouse)
DOID:0080299
  • partial lipodystrophy
Homo sapiens (human)
DOID:0080297
  • Coffin-Siris syndrome 6
Drosophila melanogaster (fruit fly)
DOID:0080297
  • Coffin-Siris syndrome 6
Homo sapiens (human)
DOID:0080297
  • Coffin-Siris syndrome 6
Mus musculus (house mouse)
DOID:0080294
  • Charcot-Marie-Tooth disease dominant intermediate G
Rattus norvegicus (Norway rat)
DOID:0080294
  • Charcot-Marie-Tooth disease dominant intermediate G
Homo sapiens (human)
DOID:0080294
  • Charcot-Marie-Tooth disease dominant intermediate G
Mus musculus (house mouse)
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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