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 15001 - 15025 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:331
  • central nervous system disease
Rattus norvegicus (Norway rat)
DOID:0111680
  • essential fructosuria
  • Aliases:
    • fructokinase deficiency
    • hepatic fructokinase deficiency
    • ketohexokinase deficiency
Homo sapiens (human)
DOID:2384
  • Wernicke encephalopathy
  • Aliases:
    • Wernicke's disease
    • Wernicke's encephalopathy
Rattus norvegicus (Norway rat)
DOID:0070112
  • Niemann-Pick disease type B
Caenorhabditis elegans
DOID:0060745
  • Doyne honeycomb retinal dystrophy
  • Aliases:
    • DHRD
    • Doyne honeycomb degeneration of retina
Mus musculus (house mouse)
DOID:5022
  • aflatoxins-related hepatocellular carcinoma
Rattus norvegicus (Norway rat)
DOID:4480
  • achondroplasia
  • Aliases:
    • Achondroplastic physique
    • Chondrodystrophia
    • osteosclerosis congenita
Xenopus laevis (African clawed frog)
DOID:4166
  • syphilis
  • Aliases:
    • syphilitic chancre
Mus musculus (house mouse)
DOID:0112363
  • spondylocostal dysostosis 5
  • Aliases:
    • SCDO5
Homo sapiens (human)
DOID:0081230
  • autosomal recessive intellectual developmental disorder 69
Homo sapiens (human)
DOID:2945
  • severe acute respiratory syndrome
  • Aliases:
    • SARS
    • SARS-CoV infection
Caenorhabditis elegans
DOID:0050630
  • Aland Island eye disease
  • Aliases:
    • FORSIUS-ERIKSSON TYPE OCULAR ALBINISM
    • Forsius-Eriksson syndrome
Homo sapiens (human)
DOID:0080200
  • bilateral renal aplasia
Homo sapiens (human)
DOID:0070146
  • hereditary sensory neuropathy type 4
  • Aliases:
    • hereditary sensory neuropathy type IV
    • insensitivity to pain, congenital, with anhidrosis
Mus musculus (house mouse)
DOID:0110919
  • hereditary spherocytosis type 4
  • Aliases:
    • HS4
    • SPH4
    • hereditary spherocytosis 4
Caenorhabditis elegans
DOID:114
  • heart disease
Mus musculus (house mouse)
DOID:9253
  • gastrointestinal stromal tumor
  • Aliases:
    • GANT
    • GIST
    • Stromal tumor of gastrointestinal tract
    • Stromal tumour of gastrointestinal tract
    • gastrointestinal stromal tumour
Rattus norvegicus (Norway rat)
DOID:0060937
  • dystonia 30
  • Aliases:
    • DYT30
Homo sapiens (human)
DOID:0111758
  • Y-linked deafness 2
  • Aliases:
    • DFNY2
Mus musculus (house mouse)
DOID:0050470
  • Donohue syndrome
  • Aliases:
    • Leprechaunism
Xenopus laevis (African clawed frog)
DOID:0060370
  • Parkinson's disease 7
  • Aliases:
    • autosomal recessive early-onset Parkinson disease 7
    • autosomal recessive early-onset Parkinson's disease 7
Mus musculus (house mouse)
DOID:2316
  • brain ischemia
  • Aliases:
    • Ischaemic encephalopathy
    • Ischemic encephalopathy
    • cerebral ischemia
Danio rerio (zebrafish)
DOID:0070277
  • primary autosomal recessive microcephaly 15
  • Aliases:
    • MCPH15
    • NEDMISBA
    • neurodevelopmental disorder with progressive microcephaly, spasticity, and brain imaging abnormalities
Danio rerio (zebrafish)
DOID:0070411
  • autosomal recessive spinocerebellar ataxia 30
  • Aliases:
    • SCAR30
Homo sapiens (human)
DOID:1068
  • juvenile glaucoma
  • Aliases:
    • Glaucoma of childhood
Rattus norvegicus (Norway rat)

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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