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 5326 - 5350 of 15957 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism Source
DOID:1827
  • idiopathic generalized epilepsy
  • Aliases:
    • Generalised epilepsy
Rattus norvegicus (Norway rat)
DOID:0112202
  • developmental and epileptic encephalopathy
Rattus norvegicus (Norway rat)
DOID:854
  • collagen disease
  • Aliases:
    • collagen disorder
Rattus norvegicus (Norway rat)
DOID:0070376
  • developmental and epileptic encephalopathy 31B
  • Aliases:
    • DEE31B
Rattus norvegicus (Norway rat)
DOID:11252
  • microcytic anemia
Rattus norvegicus (Norway rat)
DOID:0110197
  • Charcot-Marie-Tooth disease dominant intermediate B
  • Aliases:
    • CMTDI1
    • CMTDIB
    • Charcot-Marie-Tooth neuropathy dominant intermediate B
    • DI-CMTB
Rattus norvegicus (Norway rat)
DOID:0111223
  • centronuclear myopathy 1
  • Aliases:
    • CNM1
Rattus norvegicus (Norway rat)
DOID:0080437
  • developmental and epileptic encephalopathy 31A
  • Aliases:
    • DEE31
    • DEE31A
    • developmental and epileptic encephalopathy 31
    • early infantile epileptic encephalopathy 31
Rattus norvegicus (Norway rat)
DOID:0111438
  • optic atrophy 5
  • Aliases:
    • OPA5
Rattus norvegicus (Norway rat)
DOID:13711
  • dental fluorosis
  • Aliases:
    • Intrinsic enamel discolouration of fluorosis
    • Mottled teeth
    • Mottling of enamel
Rattus norvegicus (Norway rat)
DOID:0070347
  • encephalopathy due to defective mitochondrial and peroxisomal fission 1
Rattus norvegicus (Norway rat)
DOID:13711
  • dental fluorosis
  • Aliases:
    • Intrinsic enamel discolouration of fluorosis
    • Mottled teeth
    • Mottling of enamel
Mus musculus (house mouse)
DOID:0070347
  • encephalopathy due to defective mitochondrial and peroxisomal fission 1
Mus musculus (house mouse)
DOID:0111438
  • optic atrophy 5
  • Aliases:
    • OPA5
Mus musculus (house mouse)
DOID:14717
  • centronuclear myopathy
  • Aliases:
    • myotubular myopathy
Mus musculus (house mouse)
DOID:0050548
  • hereditary sensory neuropathy
  • Aliases:
    • familial dysautonomia, type II
    • hereditary sensory and autonomic neuropathy
Mus musculus (house mouse)
DOID:4926
  • bronchiolo-alveolar adenocarcinoma
  • Aliases:
    • Bronchioalveolar lung carcinoma
    • Bronchioloalveolar carcinoma
    • Minimally Invasive Lung Adenocarcinoma
Mus musculus (house mouse)
DOID:8456
  • choline deficiency disease
  • Aliases:
    • choline deficiency
Mus musculus (house mouse)
DOID:0050968
  • autosomal dominant cerebellar ataxia, deafness and narcolepsy
Mus musculus (house mouse)
DOID:0070158
  • hereditary sensory neuropathy type 1E
  • Aliases:
    • HSN1E
    • hereditary sensory neuropathy type IE
Mus musculus (house mouse)
DOID:288
  • endometriosis of uterus
  • Aliases:
    • Endometriosis interna
    • Endometriosis of myometrium
    • Endometriosis, myometrium
    • adenomyosis
    • uterine Adenomyosis
Mus musculus (house mouse)
DOID:0111951
  • immunodeficiency 40
  • Aliases:
    • DOCK2 deficiency
    • IMD40
Mus musculus (house mouse)
DOID:0080565
  • congenital disorder of glycosylation Im
  • Aliases:
    • DOLK-congenital disorder of glycosylation
    • congenital disorder of glycosylation 1m
    • dolichol kinase deficiency
Drosophila melanogaster (fruit fly)
DOID:4195
  • hyperglycemia
Drosophila melanogaster (fruit fly)
DOID:529
  • blepharospasm
Drosophila melanogaster (fruit fly)

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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