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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 11451 - 11475 of 15957 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism Source
DOID:0111678
  • hereditary folate malabsorption
  • Aliases:
    • congenital defect of folate absorption
    • congenital folate malabsorption
Rattus norvegicus (Norway rat)
DOID:0111678
  • hereditary folate malabsorption
  • Aliases:
    • congenital defect of folate absorption
    • congenital folate malabsorption
Mus musculus (house mouse)
DOID:12971
  • hereditary spherocytosis
  • Aliases:
    • Congenital spherocytic hemolytic anemia
    • Minkowski Chauffard syndrome
    • spherocytic anemia
Mus musculus (house mouse)
DOID:0110919
  • hereditary spherocytosis type 4
  • Aliases:
    • HS4
    • SPH4
    • hereditary spherocytosis 4
Mus musculus (house mouse)
DOID:2373
  • hereditary elliptocytosis
  • Aliases:
    • Congenital elliptocytosis
    • ovalocytosis
Mus musculus (house mouse)
DOID:2373
  • hereditary elliptocytosis
  • Aliases:
    • Congenital elliptocytosis
    • ovalocytosis
Rattus norvegicus (Norway rat)
DOID:12971
  • hereditary spherocytosis
  • Aliases:
    • Congenital spherocytic hemolytic anemia
    • Minkowski Chauffard syndrome
    • spherocytic anemia
Rattus norvegicus (Norway rat)
DOID:0110919
  • hereditary spherocytosis type 4
  • Aliases:
    • HS4
    • SPH4
    • hereditary spherocytosis 4
Rattus norvegicus (Norway rat)
DOID:0060649
  • congenital hereditary endothelial dystrophy of cornea
  • Aliases:
    • CHED
Mus musculus (house mouse)
DOID:0111620
  • corneal dystrophy-perceptive deafness syndrome
  • Aliases:
    • CDPD
    • CDPD1
    • Harboyan syndrome
    • corneal dystrophy and perceptive deafness
    • corneal dystrophy with progressive deafness
    • corneal endothelial dystrophy and perceptive deafness
Mus musculus (house mouse)
DOID:0110839
  • Usher syndrome type 2C
  • Aliases:
    • USH2C
    • Usher syndrome IIC
    • Usher syndrome type IIC
Rattus norvegicus (Norway rat)
DOID:0050694
  • Brown-Vialetto-Van Laere syndrome
Rattus norvegicus (Norway rat)
DOID:0080786
  • Brown-Vialetto-Van Laere syndrome 2
Rattus norvegicus (Norway rat)
DOID:8454
  • riboflavin deficiency
  • Aliases:
    • ariboflavinosis
    • vitamin B2 deficiency
Rattus norvegicus (Norway rat)
DOID:0050694
  • Brown-Vialetto-Van Laere syndrome
Mus musculus (house mouse)
DOID:8454
  • riboflavin deficiency
  • Aliases:
    • ariboflavinosis
    • vitamin B2 deficiency
Mus musculus (house mouse)
DOID:0080786
  • Brown-Vialetto-Van Laere syndrome 2
Mus musculus (house mouse)
DOID:0080785
  • Brown-Vialetto-Van Laere syndrome 1
Rattus norvegicus (Norway rat)
DOID:0080632
  • Fazio-Londe disease
  • Aliases:
    • riboflavin transporter deficiency neuronopathy
Rattus norvegicus (Norway rat)
DOID:0080785
  • Brown-Vialetto-Van Laere syndrome 1
Mus musculus (house mouse)
DOID:0080632
  • Fazio-Londe disease
  • Aliases:
    • riboflavin transporter deficiency neuronopathy
Mus musculus (house mouse)
DOID:0050718
  • vitamin metabolic disorder
Mus musculus (house mouse)
DOID:9432
  • renal glycosuria
  • Aliases:
    • renal diabetes
Mus musculus (house mouse)
DOID:9432
  • renal glycosuria
  • Aliases:
    • renal diabetes
Rattus norvegicus (Norway rat)
DOID:0050718
  • vitamin metabolic disorder
Rattus norvegicus (Norway rat)
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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