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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 12526 - 12550 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▼
DOID:0080159
  • Cryptococcal meningitis
Homo sapiens (human)
DOID:0080158
  • herpes simplex virus keratitis
  • Aliases:
    • dendritic keratitis
Rattus norvegicus (Norway rat)
DOID:0080158
  • herpes simplex virus keratitis
  • Aliases:
    • dendritic keratitis
Drosophila melanogaster (fruit fly)
DOID:0080158
  • herpes simplex virus keratitis
  • Aliases:
    • dendritic keratitis
Mus musculus (house mouse)
DOID:0080158
  • herpes simplex virus keratitis
  • Aliases:
    • dendritic keratitis
Homo sapiens (human)
DOID:0080156
  • X-linked adrenal hypoplasia congenita
  • Aliases:
    • congenital adrenal hypoplasia
Homo sapiens (human)
DOID:0080155
  • very long chain acyl-CoA dehydrogenase deficiency
  • Aliases:
    • VLCAD deficiency
Homo sapiens (human)
DOID:0080155
  • very long chain acyl-CoA dehydrogenase deficiency
  • Aliases:
    • VLCAD deficiency
Mus musculus (house mouse)
DOID:0080155
  • very long chain acyl-CoA dehydrogenase deficiency
  • Aliases:
    • VLCAD deficiency
Rattus norvegicus (Norway rat)
DOID:0080154
  • short chain acyl-CoA dehydrogenase deficiency
Rattus norvegicus (Norway rat)
DOID:0080154
  • short chain acyl-CoA dehydrogenase deficiency
Homo sapiens (human)
DOID:0080154
  • short chain acyl-CoA dehydrogenase deficiency
Mus musculus (house mouse)
DOID:0080153
  • medium chain acyl-CoA dehydrogenase deficiency
Homo sapiens (human)
DOID:0080153
  • medium chain acyl-CoA dehydrogenase deficiency
Rattus norvegicus (Norway rat)
DOID:0080153
  • medium chain acyl-CoA dehydrogenase deficiency
Mus musculus (house mouse)
DOID:0080144
  • childhood acute lymphocytic leukemia
  • Aliases:
    • Childhood Acute Lymphoblastic Leukemia
Homo sapiens (human)
DOID:0080143
  • congenital fibrosis of the extraocular muscles
Homo sapiens (human)
DOID:0080143
  • congenital fibrosis of the extraocular muscles
Mus musculus (house mouse)
DOID:0080142
  • mosaic variegated aneuploidy syndrome 2
Homo sapiens (human)
DOID:0080141
  • mosaic variegated aneuploidy syndrome 1
Homo sapiens (human)
DOID:0080140
  • multiple congenital anomalies-hypotonia-seizures syndrome 3
  • Aliases:
    • M syndrome
    • light fixation seizure syndrome
Caenorhabditis elegans
DOID:0080140
  • multiple congenital anomalies-hypotonia-seizures syndrome 3
  • Aliases:
    • M syndrome
    • light fixation seizure syndrome
Saccharomyces cerevisiae S288C
DOID:0080140
  • multiple congenital anomalies-hypotonia-seizures syndrome 3
  • Aliases:
    • M syndrome
    • light fixation seizure syndrome
Mus musculus (house mouse)
DOID:0080140
  • multiple congenital anomalies-hypotonia-seizures syndrome 3
  • Aliases:
    • M syndrome
    • light fixation seizure syndrome
Homo sapiens (human)
DOID:0080139
  • multiple congenital anomalies-hypotonia-seizures syndrome 2
  • Aliases:
    • developmental and epileptic encephalopathy 20
    • early infantile epileptic encephalopathy 20
    • glycosylphosphatidylinositol biosynthesis defect 4
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