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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 8376 - 8400 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism Source
DOID:0110217
  • Leber congenital amaurosis 17
  • Aliases:
    • LCA17
Rattus norvegicus (Norway rat)
DOID:0080589
  • Klippel-Feil syndrome 1
Rattus norvegicus (Norway rat)
DOID:0081320
  • multiple synostoses syndrome 4
Rattus norvegicus (Norway rat)
DOID:0080155
  • very long chain acyl-CoA dehydrogenase deficiency
  • Aliases:
    • VLCAD deficiency
Rattus norvegicus (Norway rat)
DOID:0112072
  • nuclear type mitochondrial complex I deficiency 20
  • Aliases:
    • ACAD9 deficiency
    • Acyl-CoA dehydrogenase 9 deficiency
    • MC1DN20
    • mitochondrial complex 1 deficiency due to ACAD9 deficiency
Rattus norvegicus (Norway rat)
DOID:0110896
  • inflammatory bowel disease 16
  • Aliases:
    • IBD16
Rattus norvegicus (Norway rat)
DOID:0060558
  • lethal congenital contracture syndrome
Rattus norvegicus (Norway rat)
DOID:7725
  • epilepsy with generalized tonic-clonic seizures
  • Aliases:
    • Epileptic seizures, tonic-clonic
    • Grand Mal epilepsy
    • tonic-clonic epilepsy
Rattus norvegicus (Norway rat)
DOID:0060748
  • familial temporal lobe epilepsy 1
  • Aliases:
    • ETL1
    • partial epilepsy with auditory features
Rattus norvegicus (Norway rat)
DOID:0070388
  • developmental and epileptic encephalopathy 102
  • Aliases:
    • DEE102
    • early infantile epileptic encephalopathy 102
Rattus norvegicus (Norway rat)
DOID:8869
  • neuromyelitis optica
  • Aliases:
    • Devic's disease
    • Devic's syndrome
Rattus norvegicus (Norway rat)
DOID:9849
  • Meniere's disease
  • Aliases:
    • Meniere disease
    • Mnire's vertigo
    • Otogenic vertigo
Rattus norvegicus (Norway rat)
DOID:0080743
  • transverse myelitis
Rattus norvegicus (Norway rat)
DOID:0080122
  • Alpers-Huttenlocher syndrome
  • Aliases:
    • Alper's syndrome
    • Alpers disease
    • Alpers progressive infantile poliodystrophy
    • Alpers syndrome
    • Alpers' disease or gray-matter degeneration
    • Diffuse Cerebral Sclerosis of Schilder
    • mitochondrial DNA depletion syndrome 4a
    • progressive sclerosing poliodystrophy
Rattus norvegicus (Norway rat)
DOID:3275
  • thymoma
Rattus norvegicus (Norway rat)
DOID:0080315
  • megalencephalic leukoencephalopathy with subcortical cysts
  • Aliases:
    • megalencephalic leukodystrophy megalencephaly-cystic leukodystorphy syndrome
    • vacuolating megalencephalic leukoencephalopathy with subcortical cysts
Rattus norvegicus (Norway rat)
DOID:1432
  • blindness
  • Aliases:
    • vision impairment
    • vision loss
    • visual impairment
Rattus norvegicus (Norway rat)
DOID:3762
  • cytochrome-c oxidase deficiency disease
  • Aliases:
    • MITOCHONDRIAL COMPLEX IV DEFICIENCY
Rattus norvegicus (Norway rat)
DOID:0070505
  • mitochondrial complex IV deficiency nuclear type 20
  • Aliases:
    • MC4DN20
Rattus norvegicus (Norway rat)
DOID:0060340
  • ciliopathy
Rattus norvegicus (Norway rat)
DOID:0080669
  • posterior polymorphous corneal dystrophy 4
Mus musculus (house mouse)
DOID:0110557
  • autosomal dominant nonsyndromic deafness 28
  • Aliases:
    • DFNA28
    • autosomal dominant deafness 28
Mus musculus (house mouse)
DOID:0110540
  • autosomal recessive nonsyndromic deafness 98
  • Aliases:
    • DFNB98
    • autosomal recessive deafness 98
Mus musculus (house mouse)
DOID:0111662
  • ectodermal dysplasia 14
  • Aliases:
    • ECTN14
    • ectodermal dysplasia 14, hair/tooth type with or without hypohidrosis
Mus musculus (house mouse)
DOID:2044
  • drug-induced hepatitis
  • Aliases:
    • Drug-induced chronic hepatitis
Rattus norvegicus (Norway rat)
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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