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 14226 - 14250 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism Source
DOID:0110831
  • Usher syndrome type 1D
  • Aliases:
    • USH1D
    • Usher syndrome type ID
Rattus norvegicus (Norway rat)
DOID:0050565
  • autosomal recessive nonsyndromic deafness
Rattus norvegicus (Norway rat)
DOID:0060681
  • autosomal dominant nocturnal frontal lobe epilepsy
  • Aliases:
    • ENFL
Homo sapiens (human)
DOID:0060684
  • autosomal dominant nocturnal frontal lobe epilepsy 3
  • Aliases:
    • ENFL3
    • nocturnal frontal lobe epilepsy 3
Homo sapiens (human)
DOID:0050848
  • obstructive sleep apnea
  • Aliases:
    • obstructive sleep apnea syndrome
Rattus norvegicus (Norway rat)
DOID:1205
  • allergic disease
  • Aliases:
    • allergic hypersensitivity disease
    • hypersensitivity
    • hypersensitivity reaction type I disease
Rattus norvegicus (Norway rat)
DOID:6432
  • pulmonary hypertension
Rattus norvegicus (Norway rat)
DOID:3770
  • pulmonary fibrosis
  • Aliases:
    • Fibrosis of lung
Rattus norvegicus (Norway rat)
DOID:0112147
  • retinitis pigmentosa 90
  • Aliases:
    • RP90
Rattus norvegicus (Norway rat)
DOID:0050709
  • early infantile epileptic encephalopathy
  • Aliases:
    • Early Infantile Epileptic Encephalopathy with Burst-Suppression
Rattus norvegicus (Norway rat)
DOID:439
  • neuromuscular junction disease
Rattus norvegicus (Norway rat)
DOID:0080154
  • short chain acyl-CoA dehydrogenase deficiency
Mus musculus (house mouse)
DOID:1928
  • Williams-Beuren syndrome
  • Aliases:
    • Fanconi Schlesinger syndrome
    • WBS
Homo sapiens (human)
DOID:0060276
  • pontocerebellar hypoplasia type 7
Homo sapiens (human)
DOID:0060264
  • pontocerebellar hypoplasia
  • Aliases:
    • PCH
Homo sapiens (human)
DOID:3534
  • Lafora disease
  • Aliases:
    • Lafora Progressive Myoclonic Epilepsy
    • Lafora's disease
    • MYOCLONIC EPILEPSY OF LAFORA
Rattus norvegicus (Norway rat)
DOID:891
  • progressive myoclonus epilepsy
  • Aliases:
    • PME
    • progressive myoclonic epilepsy
Rattus norvegicus (Norway rat)
DOID:14227
  • azoospermia
Rattus norvegicus (Norway rat)
DOID:1059
  • intellectual disability
Rattus norvegicus (Norway rat)
DOID:0060041
  • autism spectrum disorder
Rattus norvegicus (Norway rat)
DOID:0110681
  • congenital myasthenic syndrome 2A
  • Aliases:
    • CMS2A
    • congenital myasthenic syndrome 2A slow-channel
Homo sapiens (human)
DOID:0110680
  • congenital myasthenic syndrome 2C
  • Aliases:
    • CMS2C
    • congenital myasthenic syndrome 2C associated with acetylcholine receptor deficiency
Homo sapiens (human)
DOID:2043
  • hepatitis B
  • Aliases:
    • chronic hepatitis B
    • hepatitis B infection
Rattus norvegicus (Norway rat)
DOID:0070215
  • familial hyperinsulinemic hypoglycemia 4
  • Aliases:
    • HHF4
    • hyperinsulinemic hypoglycemia due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency
    • hyperinsulinism due to SCHAD deficiency
    • hyperinsulinism due to glutamodehydrogenase deficiency
    • hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency
Rattus norvegicus (Norway rat)
DOID:5844
  • myocardial infarction
  • Aliases:
    • Myocardial infarct
    • heart attack
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