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 13701 - 13725 of 15957 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism Source
DOID:12387
  • nephrogenic diabetes insipidus
Rattus norvegicus (Norway rat)
DOID:0081061
  • nephrogenic diabetes insipidus type 2
  • Aliases:
    • autosomal nephrogenic diabetes insipidus-2
Mus musculus (house mouse)
DOID:1837
  • diabetic ketoacidosis
  • Aliases:
    • DIABETES MELLITUS, KETOSIS-PRONE
    • ketosis-prone diabetes mellitus
Mus musculus (house mouse)
DOID:9409
  • diabetes insipidus
Mus musculus (house mouse)
DOID:12387
  • nephrogenic diabetes insipidus
Mus musculus (house mouse)
DOID:9428
  • intracranial hypertension
  • Aliases:
    • Raised intracranial pressure
Rattus norvegicus (Norway rat)
DOID:636
  • central pontine myelinolysis
  • Aliases:
    • osmotic demyelination syndrome
Rattus norvegicus (Norway rat)
DOID:1727
  • retinal vein occlusion
  • Aliases:
    • Occlusion, of retinal vein
Rattus norvegicus (Norway rat)
DOID:9428
  • intracranial hypertension
  • Aliases:
    • Raised intracranial pressure
Mus musculus (house mouse)
DOID:636
  • central pontine myelinolysis
  • Aliases:
    • osmotic demyelination syndrome
Mus musculus (house mouse)
DOID:1727
  • retinal vein occlusion
  • Aliases:
    • Occlusion, of retinal vein
Mus musculus (house mouse)
DOID:1919
  • Lesch-Nyhan syndrome
  • Aliases:
    • Complete hypoxanthine-guanine phosphoribosyltransferase deficiency
    • HG-PRT deficiency
    • Hypoxanthine-guanine phosphoribosyltransferase deficiency
    • Hypoxanthine-guanine-phosphoribosyltransferase deficiency
    • Lesch - Nyhan syndrome
    • X-linked hyperuricemia
    • deficiency of IMP pyrophosphorylase
    • hypoxanthine guanine phosphoribosyltransferase deficiency
Drosophila melanogaster (fruit fly)
DOID:0060350
  • adenine phosphoribosyltransferase deficiency
  • Aliases:
    • 2,8-dihydroxyadenine urolithiasis
    • APRT deficiency
Drosophila melanogaster (fruit fly)
DOID:0060350
  • adenine phosphoribosyltransferase deficiency
  • Aliases:
    • 2,8-dihydroxyadenine urolithiasis
    • APRT deficiency
Rattus norvegicus (Norway rat)
DOID:1919
  • Lesch-Nyhan syndrome
  • Aliases:
    • Complete hypoxanthine-guanine phosphoribosyltransferase deficiency
    • HG-PRT deficiency
    • Hypoxanthine-guanine phosphoribosyltransferase deficiency
    • Hypoxanthine-guanine-phosphoribosyltransferase deficiency
    • Lesch - Nyhan syndrome
    • X-linked hyperuricemia
    • deficiency of IMP pyrophosphorylase
    • hypoxanthine guanine phosphoribosyltransferase deficiency
Rattus norvegicus (Norway rat)
DOID:0060350
  • adenine phosphoribosyltransferase deficiency
  • Aliases:
    • 2,8-dihydroxyadenine urolithiasis
    • APRT deficiency
Mus musculus (house mouse)
DOID:1919
  • Lesch-Nyhan syndrome
  • Aliases:
    • Complete hypoxanthine-guanine phosphoribosyltransferase deficiency
    • HG-PRT deficiency
    • Hypoxanthine-guanine phosphoribosyltransferase deficiency
    • Hypoxanthine-guanine-phosphoribosyltransferase deficiency
    • Lesch - Nyhan syndrome
    • X-linked hyperuricemia
    • deficiency of IMP pyrophosphorylase
    • hypoxanthine guanine phosphoribosyltransferase deficiency
Mus musculus (house mouse)
DOID:0070028
  • APP-related cerebral amyloid angiopathy
  • Aliases:
    • Amyloidosis, Cerebroarterial, App-Related
    • Amyloidosis, Hereditary, With Cerebral Hemorrhage, Dutch Variant
    • Cerebral Amyloid Angiopathy, App-Related, Arctic Variant
    • Cerebral Amyloid Angiopathy, App-Related, Dutch Variant
    • Cerebral Amyloid Angiopathy, App-Related, Flemish Variant
    • Cerebral Amyloid Angiopathy, App-Related, Iowa Variant
    • Cerebral Amyloid Angiopathy, App-Related, Italian Variant
    • HCHWAD
Drosophila melanogaster (fruit fly)
DOID:0050850
  • diabetic encephalopathy
Drosophila melanogaster (fruit fly)
DOID:0080348
  • Alzheimer's disease 1
  • Aliases:
    • Alzheimer's disease 1, early onset
Drosophila melanogaster (fruit fly)
DOID:1561
  • cognitive disorder
  • Aliases:
    • cognitive disease
Drosophila melanogaster (fruit fly)
DOID:824
  • periodontitis
  • Aliases:
    • chronic pericementitis
Drosophila melanogaster (fruit fly)
DOID:11758
  • iron deficiency anemia
Drosophila melanogaster (fruit fly)
DOID:11832
  • visual epilepsy
  • Aliases:
    • epilepsy, visual
Drosophila melanogaster (fruit fly)
DOID:0081292
  • traumatic brain injury
Drosophila melanogaster (fruit fly)

About Release Notes Help Feedback

Click here to visit the beta site.


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