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 6401 - 6425 of 7942 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism
DOID:0080501
  • GM1 gangliosidosis type 2
  • Aliases:
    • juvenile GM1 gangliosidosis
Mus musculus (house mouse)
DOID:0080492
  • leukocyte adhesion deficiency 2
Homo sapiens (human)
DOID:0080491
  • cerebral cavernous malformation 1
Homo sapiens (human)
DOID:0080490
  • mucolipidosis type IV
Homo sapiens (human)
DOID:0080489
  • GM1 gangliosidosis type 3
  • Aliases:
    • adult-onset GM1 gangliosidosis
Homo sapiens (human)
DOID:0080489
  • GM1 gangliosidosis type 3
  • Aliases:
    • adult-onset GM1 gangliosidosis
Mus musculus (house mouse)
DOID:0080488
  • mucolipidosis
Mus musculus (house mouse)
DOID:0080488
  • mucolipidosis
Danio rerio (zebrafish)
DOID:0080488
  • mucolipidosis
Homo sapiens (human)
DOID:0080484
  • peroxisome biogenesis disorder 10A
  • Aliases:
    • peroxisome biogenesis disorder 10A (Zellweger)
Homo sapiens (human)
DOID:0080483
  • peroxisome biogenesis disorder 8A
  • Aliases:
    • peroxisome biogenesis disorder 8A (Zellweger)
Homo sapiens (human)
DOID:0080482
  • peroxisome biogenesis disorder 7A
  • Aliases:
    • peroxisome biogenesis disorder 7A (Zellweger)
Homo sapiens (human)
DOID:0080480
  • peroxisome biogenesis disorder 5A
  • Aliases:
    • peroxisome biogenesis disorder 5A (Zellweger)
Homo sapiens (human)
DOID:0080479
  • peroxisome biogenesis disorder 4A
  • Aliases:
    • peroxisome biogenesis disorder 4A (Zellweger)
Homo sapiens (human)
DOID:0080476
  • peroxisome biogenesis disorder 1A
  • Aliases:
    • peroxisome biogenesis disorder 1A (Zellweger)
Homo sapiens (human)
DOID:0080473
  • developmental delay and seizures with or without movement abnormalities
Homo sapiens (human)
DOID:0080470
  • developmental and epileptic encephalopathy 36
  • Aliases:
    • congenital disorder of glycosylation, type Is
    • early infantile epileptic encephalopathy 36
Homo sapiens (human)
DOID:0080470
  • developmental and epileptic encephalopathy 36
  • Aliases:
    • congenital disorder of glycosylation, type Is
    • early infantile epileptic encephalopathy 36
Mus musculus (house mouse)
DOID:0080470
  • developmental and epileptic encephalopathy 36
  • Aliases:
    • congenital disorder of glycosylation, type Is
    • early infantile epileptic encephalopathy 36
Xenopus tropicalis (tropical clawed frog)
DOID:0080470
  • developmental and epileptic encephalopathy 36
  • Aliases:
    • congenital disorder of glycosylation, type Is
    • early infantile epileptic encephalopathy 36
Rattus norvegicus (Norway rat)
DOID:0080470
  • developmental and epileptic encephalopathy 36
  • Aliases:
    • congenital disorder of glycosylation, type Is
    • early infantile epileptic encephalopathy 36
Danio rerio (zebrafish)
DOID:0080470
  • developmental and epileptic encephalopathy 36
  • Aliases:
    • congenital disorder of glycosylation, type Is
    • early infantile epileptic encephalopathy 36
Xenopus laevis (African clawed frog)
DOID:0080470
  • developmental and epileptic encephalopathy 36
  • Aliases:
    • congenital disorder of glycosylation, type Is
    • early infantile epileptic encephalopathy 36
Caenorhabditis elegans
DOID:0080470
  • developmental and epileptic encephalopathy 36
  • Aliases:
    • congenital disorder of glycosylation, type Is
    • early infantile epileptic encephalopathy 36
Saccharomyces cerevisiae S288C
DOID:0080468
  • developmental and epileptic encephalopathy 1
  • Aliases:
    • DEE1
    • X-linked infantile spasm syndrome 1
    • early infantile epileptic encephalopathy 1
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