GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources July 29, 2024
DisGeNET July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 1351 - 1375 of 7942 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism
DOID:0080139
  • multiple congenital anomalies-hypotonia-seizures syndrome 2
  • Aliases:
    • developmental and epileptic encephalopathy 20
    • early infantile epileptic encephalopathy 20
    • glycosylphosphatidylinositol biosynthesis defect 4
Saccharomyces cerevisiae S288C
DOID:0080140
  • multiple congenital anomalies-hypotonia-seizures syndrome 3
  • Aliases:
    • M syndrome
    • light fixation seizure syndrome
Homo sapiens (human)
DOID:0080141
  • mosaic variegated aneuploidy syndrome 1
Homo sapiens (human)
DOID:0080144
  • childhood acute lymphocytic leukemia
  • Aliases:
    • Childhood Acute Lymphoblastic Leukemia
Homo sapiens (human)
DOID:0080145
  • childhood T-cell acute lymphoblastic leukemia
  • Aliases:
    • T-cell childhood acute lymphocytic leukemia
    • childhood precursor T-lymphoblastic lymphoma/leukemia
Homo sapiens (human)
DOID:0080146
  • childhood B-cell acute lymphoblastic leukemia
Homo sapiens (human)
DOID:0080147
  • lymphoblastic lymphoma
Homo sapiens (human)
DOID:0080148
  • T-cell childhood lymphoblastic lymphoma
  • Aliases:
    • Childhood T lymphoblastic lymphoma
Homo sapiens (human)
DOID:0080149
  • adult acute monocytic leukemia
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:0080153
  • medium chain acyl-CoA dehydrogenase deficiency
Homo sapiens (human)
DOID:0080154
  • short chain acyl-CoA dehydrogenase deficiency
Homo sapiens (human)
DOID:0080155
  • very long chain acyl-CoA dehydrogenase deficiency
  • Aliases:
    • VLCAD deficiency
Homo sapiens (human)
DOID:0080156
  • X-linked adrenal hypoplasia congenita
  • Aliases:
    • congenital adrenal hypoplasia
Homo sapiens (human)
DOID:0080158
  • herpes simplex virus keratitis
  • Aliases:
    • dendritic keratitis
Homo sapiens (human)
DOID:0080158
  • herpes simplex virus keratitis
  • Aliases:
    • dendritic keratitis
Mus musculus (house mouse)
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:0080159
  • Cryptococcal meningitis
Homo sapiens (human)
DOID:0080160
  • Cytomegalovirus retinitis
  • Aliases:
    • CMV retinitis
Homo sapiens (human)
DOID:0080161
  • cutaneous candidiasis
Homo sapiens (human)
DOID:0080162
  • lupus nephritis
Rattus norvegicus (Norway rat)
DOID:0080162
  • lupus nephritis
Mus musculus (house mouse)
DOID:0080162
  • lupus nephritis
Homo sapiens (human)

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024