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 1276 - 1300 of 4649 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism Source
DOID:0080463
  • developmental and epileptic encephalopathy 33
  • Aliases:
    • DEE33
    • early infantile epileptic encephalopathy 33
Homo sapiens (human)
DOID:0080464
  • developmental and epileptic encephalopathy 53
  • Aliases:
    • DEE53
    • early infantile epileptic encephalopathy 53
Homo sapiens (human)
DOID:0080465
  • developmental and epileptic encephalopathy 30
  • Aliases:
    • DEE30
    • early infantile epileptic encephalopathy 30
Homo sapiens (human)
DOID:0080467
  • developmental and epileptic encephalopathy 2
  • Aliases:
    • DEE2
    • EIEE2
    • X-linked infantile spasm syndrome 2
    • early infantile epileptic encephalopathy 2
Homo sapiens (human)
DOID:0080468
  • developmental and epileptic encephalopathy 1
  • Aliases:
    • DEE1
    • X-linked infantile spasm syndrome 1
    • early infantile epileptic encephalopathy 1
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:0080471
  • developmental and epileptic encephalopathy 92
Homo sapiens (human)
DOID:0080472
  • developmental and epileptic encephalopathy 91
  • Aliases:
    • infantile or early childhood epileptic encephalopathy 1
Homo sapiens (human)
DOID:0080473
  • developmental delay and seizures with or without movement abnormalities
Homo sapiens (human)
DOID:0080475
  • psoriasis 2
Homo sapiens (human)
DOID:0080484
  • peroxisome biogenesis disorder 10A
  • Aliases:
    • peroxisome biogenesis disorder 10A (Zellweger)
Homo sapiens (human)
DOID:0080486
  • peroxisome biogenesis disorder 12A
  • Aliases:
    • peroxisome biogenesis disorder 12A (Zellweger)
Homo sapiens (human)
DOID:0080487
  • peroxisome biogenesis disorder 13A
  • Aliases:
    • peroxisome biogenesis disorder 13A (Zellweger)
Homo sapiens (human)
DOID:0080488
  • mucolipidosis
Homo sapiens (human)
DOID:0080489
  • GM1 gangliosidosis type 3
  • Aliases:
    • adult-onset GM1 gangliosidosis
Homo sapiens (human)
DOID:0080490
  • mucolipidosis type IV
Homo sapiens (human)
DOID:0080491
  • cerebral cavernous malformation 1
Homo sapiens (human)
DOID:0080493
  • ovarian dysgenesis 1
Homo sapiens (human)
DOID:0080494
  • ovarian dysgenesis 2
Homo sapiens (human)
DOID:0080498
  • ovarian dysgenesis 6
Homo sapiens (human)
DOID:0080499
  • ovarian dysgenesis 7
Homo sapiens (human)
DOID:0080501
  • GM1 gangliosidosis type 2
  • Aliases:
    • juvenile GM1 gangliosidosis
Homo sapiens (human)
DOID:0080502
  • GM1 gangliosidosis type 1
Homo sapiens (human)
DOID:0080505
  • Cornelia de Lange syndrome 1
Homo sapiens (human)
DOID:0080506
  • Cornelia de Lange syndrome 2
Homo sapiens (human)

About Release Notes Help Feedback

International Collaboration

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.1.0

Last updated: December 9, 2024