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 176 - 200 of 4649 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▲
DOID:0050722
  • PHGDH deficiency
  • Aliases:
    • PHOSPHOGLYCERATE DEHYDROGENASE DEFICIENCY
Homo sapiens (human)
DOID:0050723
  • PSAT deficiency
  • Aliases:
    • Phosphoserine aminotransferase deficiency
Homo sapiens (human)
DOID:0050729
  • Chanarin-Dorfman syndrome
  • Aliases:
    • neutral lipid storage disease
Homo sapiens (human)
DOID:0050730
  • coenzyme Q10 deficiency disease
  • Aliases:
    • COENZYME Q10 DEFICIENCY, PRIMARY
Homo sapiens (human)
DOID:0050731
  • vitamin B12 deficiency
  • Aliases:
    • cobalamin deficiency
    • hypocobalaminemia
Homo sapiens (human)
DOID:0050733
  • methylmalonic aciduria and homocystinuria type cblG
Homo sapiens (human)
DOID:0050734
  • congenital intrinsic factor deficiency
  • Aliases:
    • hereditary intrinsic factor deficiency
Homo sapiens (human)
DOID:0050736
  • autosomal dominant disease
Homo sapiens (human)
DOID:0050737
  • autosomal recessive disease
Homo sapiens (human)
DOID:0050741
  • alcohol dependence
  • Aliases:
    • alcoholism
Homo sapiens (human)
DOID:0050742
  • nicotine dependence
  • Aliases:
    • tobacco use disorder
Homo sapiens (human)
DOID:0050744
  • anaplastic large cell lymphoma
Homo sapiens (human)
DOID:0050745
  • diffuse large B-cell lymphoma
  • Aliases:
    • DLBCL
Homo sapiens (human)
DOID:0050746
  • mantle cell lymphoma
Homo sapiens (human)
DOID:0050748
  • marginal zone lymphoma
  • Aliases:
    • marginal zone B-cell lymphoma
Homo sapiens (human)
DOID:0050749
  • peripheral T-cell lymphoma
Homo sapiens (human)
DOID:0050750
  • splenic marginal zone lymphoma
Homo sapiens (human)
DOID:0050752
  • amyotrophic lateral sclerosis type 8
  • Aliases:
    • ALS8
    • amyotrophic lateral sclerosis 8
Homo sapiens (human)
DOID:0050753
  • cerebellar ataxia
Homo sapiens (human)
DOID:0050754
  • ataxia with oculomotor apraxia type 1
Homo sapiens (human)
DOID:0050755
  • spinocerebellar ataxia with axonal neuropathy 2
  • Aliases:
    • AOA2
    • SCAN2
    • SCAR1
    • ataxia with oculomotor apraxia type 2
    • autosomal recessive spinocerebellar ataxia 1
    • autosomal recessive spinocerebellar ataxia with axonal neuropathy 2
    • spinocerebellar ataxia with axonal neuropathy type 2
Homo sapiens (human)
DOID:0050758
  • metabolic acidosis
Homo sapiens (human)
DOID:0050759
  • myotonic dystrophy type 2
Homo sapiens (human)
DOID:0050763
  • ARC syndrome
  • Aliases:
    • ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS
    • Arthrogryposis, renal dysfunction and cholestasis (ARC) syndrome
    • Arthrogryposis-renal dysfunction-cholestasis
Homo sapiens (human)
DOID:0050766
  • choreaacanthocytosis
  • Aliases:
    • Levine-Critchley syndrome
    • choreo-acanthocytosis
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