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 13501 - 13525 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism Source
DOID:5679
  • retinal disease
Mus musculus (house mouse)
DOID:1210
  • optic neuritis
Mus musculus (house mouse)
DOID:8869
  • neuromyelitis optica
  • Aliases:
    • Devic's disease
    • Devic's syndrome
Mus musculus (house mouse)
DOID:12365
  • malaria
  • Aliases:
    • induced malaria
Mus musculus (house mouse)
DOID:332
  • amyotrophic lateral sclerosis
  • Aliases:
    • ALS
    • Lou Gehrig's disease
    • motor neuron disease, bulbar
Mus musculus (house mouse)
DOID:1432
  • blindness
  • Aliases:
    • vision impairment
    • vision loss
    • visual impairment
Mus musculus (house mouse)
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
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:4724
  • brain edema
  • Aliases:
    • intracranial swelling
    • wet brain
Mus musculus (house mouse)
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
Mus musculus (house mouse)
DOID:11758
  • iron deficiency anemia
Mus musculus (house mouse)
DOID:0110731
  • neuronal ceroid lipofuscinosis 3
  • Aliases:
    • Batten disease
    • CLN3
    • juvenile neuronal ceroid lipofuscinosis
Homo sapiens (human)
DOID:0111815
  • low molecular weight proteinuria with hypercalciuric nephrocalcinosis
Homo sapiens (human)
DOID:0050699
  • Dent disease
  • Aliases:
    • Dent disease 1
    • Dent disease 2
    • Dent's disease
Homo sapiens (human)
DOID:13533
  • osteopetrosis
  • Aliases:
    • Albers-Schonberg disease
    • marble bone
Homo sapiens (human)
DOID:0080943
  • 46,XX sex reversal 5
Mus musculus (house mouse)
DOID:2988
  • antiphospholipid syndrome
  • Aliases:
    • APS
    • antiphospholipid antibody syndrome
Mus musculus (house mouse)
DOID:341
  • peripheral vascular disease
  • Aliases:
    • arterial occlusive disease
Mus musculus (house mouse)

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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


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Last updated: December 9, 2024