GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources July 29, 2024
DisGeNET July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 4851 - 4875 of 7942 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism
DOID:0111626
  • D-glyceric aciduria
  • Aliases:
    • D-glycerate kinase deficiency
    • D-glyceric acidemia
    • D-glycericacidemia
    • deficiency of glycerate kinase
    • non ketotic hyperglycinemia syndrome
Rattus norvegicus (Norway rat)
DOID:0111626
  • D-glyceric aciduria
  • Aliases:
    • D-glycerate kinase deficiency
    • D-glyceric acidemia
    • D-glycericacidemia
    • deficiency of glycerate kinase
    • non ketotic hyperglycinemia syndrome
Mus musculus (house mouse)
DOID:0111619
  • combined D-2- and L-2-hydroxyglutaric aciduria
  • Aliases:
    • D,L-2-HGA
    • D,L-2-hydroxyglutaric acidemia
    • D,L-2-hydroxyglutaric aciduria
    • combined D,L-2-hydroxyglutaric aciduria
    • combined D-2-hydroxyglutaric acidemia and L-2-hydroxyglutaric acidemia
    • combined D-2-hydroxyglutaric aciduria and L-2-hydroxyglutaric aciduria
Homo sapiens (human)
DOID:0111582
  • hereditary arterial and articular multiple calcification syndrome
  • Aliases:
    • CALJA
    • arterial calcification and distal joint calcification
    • arterial calcification due to CD73 deficiency
    • arterial calcification due to deficiency of CD73
    • calcification of joints and arteries
Homo sapiens (human)
DOID:0111532
  • osteoglophonic dysplasia
  • Aliases:
    • Fairbank-Keats syndrome
    • OGD
    • osteoglophonic dwarfism
Homo sapiens (human)
DOID:0111531
  • bilateral optic nerve hypoplasia
  • Aliases:
    • ONH
    • familial bilateral optic nerve hypoplasia
    • isolated optic nerve hypoplasia/aplasia
Homo sapiens (human)
DOID:0111530
  • linear nevus sebaceous syndrome
  • Aliases:
    • JNP
    • Jadassohn nevus phakomatosis
    • SFM syndrome
    • Schimmelpenning Feuerstein Mims syndrome
    • Schimmelpenning syndrome
    • Solomon syndrome
    • nevus sebaceus of Jadassohn
    • nevus sebaceus syndrome
    • organoid nevus phakomatosis
    • organoid nevus syndrome
Homo sapiens (human)
DOID:0111529
  • familial multiple nevi flammei
  • Aliases:
    • CMC
    • congenital capillary malformations
    • familial multiple port-wine stains
Homo sapiens (human)
DOID:0111527
  • spinal muscular atrophy with progressive myoclonic epilepsy
  • Aliases:
    • Jankovic-Rivera syndrome
    • SMA-PME
    • SMAPME
    • hereditary myoclonus-progressive distal muscular atrophy syndrome
Homo sapiens (human)
DOID:0111512
  • metachondromatosis
  • Aliases:
    • METCDS
Homo sapiens (human)
DOID:0111507
  • Lenz-Majewski hyperostotic dwarfism
  • Aliases:
    • Lenz-Majewski syndrome
Homo sapiens (human)
DOID:0111503
  • Li-Fraumeni syndrome 1
  • Aliases:
    • LFS1
Rattus norvegicus (Norway rat)
DOID:0111503
  • Li-Fraumeni syndrome 1
  • Aliases:
    • LFS1
Mus musculus (house mouse)
DOID:0111503
  • Li-Fraumeni syndrome 1
  • Aliases:
    • LFS1
Homo sapiens (human)
DOID:0111460
  • cardiofaciocutaneous syndrome 1
  • Aliases:
    • CFC1
Homo sapiens (human)
DOID:0111460
  • cardiofaciocutaneous syndrome 1
  • Aliases:
    • CFC1
Mus musculus (house mouse)
DOID:0111459
  • classic galactosemia
  • Aliases:
    • GALT deficiency
    • galactose-1-phosphate uridyltransferase deficiency
    • galactosemia type 1
Caenorhabditis elegans
DOID:0111459
  • classic galactosemia
  • Aliases:
    • GALT deficiency
    • galactose-1-phosphate uridyltransferase deficiency
    • galactosemia type 1
Saccharomyces cerevisiae S288C
DOID:0111459
  • classic galactosemia
  • Aliases:
    • GALT deficiency
    • galactose-1-phosphate uridyltransferase deficiency
    • galactosemia type 1
Homo sapiens (human)
DOID:0111459
  • classic galactosemia
  • Aliases:
    • GALT deficiency
    • galactose-1-phosphate uridyltransferase deficiency
    • galactosemia type 1
Mus musculus (house mouse)
DOID:0111459
  • classic galactosemia
  • Aliases:
    • GALT deficiency
    • galactose-1-phosphate uridyltransferase deficiency
    • galactosemia type 1
Drosophila melanogaster (fruit fly)
DOID:0111459
  • classic galactosemia
  • Aliases:
    • GALT deficiency
    • galactose-1-phosphate uridyltransferase deficiency
    • galactosemia type 1
Rattus norvegicus (Norway rat)
DOID:0111458
  • galactose epimerase deficiency
  • Aliases:
    • GALE deficiency
    • GALE-D
    • UDP-galactose-4-epimerase deficiency
    • epimerase deficiency galactosemia
    • galactosemia III
    • galactosemia type 3
    • uridine diphosphate galactose-4-epimerase deficiency
Saccharomyces cerevisiae S288C
DOID:0111458
  • galactose epimerase deficiency
  • Aliases:
    • GALE deficiency
    • GALE-D
    • UDP-galactose-4-epimerase deficiency
    • epimerase deficiency galactosemia
    • galactosemia III
    • galactosemia type 3
    • uridine diphosphate galactose-4-epimerase deficiency
Homo sapiens (human)
DOID:0111458
  • galactose epimerase deficiency
  • Aliases:
    • GALE deficiency
    • GALE-D
    • UDP-galactose-4-epimerase deficiency
    • epimerase deficiency galactosemia
    • galactosemia III
    • galactosemia type 3
    • uridine diphosphate galactose-4-epimerase deficiency
Drosophila melanogaster (fruit fly)

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Last updated: August 19, 2024