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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 9351 - 9375 of 15957 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism Source
DOID:655
  • inherited metabolic disorder
  • Aliases:
    • Inborn Errors of Metabolism
    • Metabolic hereditary disorder
    • inborn metabolism disorder
Rattus norvegicus (Norway rat)
DOID:0112068
  • nuclear type mitochondrial complex I deficiency 5
  • Aliases:
    • MC1DN5
Rattus norvegicus (Norway rat)
DOID:0112066
  • nuclear type mitochondrial complex I deficiency 6
  • Aliases:
    • MC1DN6
Rattus norvegicus (Norway rat)
DOID:0112074
  • nuclear type mitochondrial complex I deficiency 1
  • Aliases:
    • MC1DN1
Mus musculus (house mouse)
DOID:0112074
  • nuclear type mitochondrial complex I deficiency 1
  • Aliases:
    • MC1DN1
Rattus norvegicus (Norway rat)
DOID:0112083
  • nuclear type mitochondrial complex I deficiency 2
  • Aliases:
    • MC1DN2
Mus musculus (house mouse)
DOID:0112083
  • nuclear type mitochondrial complex I deficiency 2
  • Aliases:
    • MC1DN2
Rattus norvegicus (Norway rat)
DOID:0112092
  • nuclear type mitochondrial complex I deficiency 7
  • Aliases:
    • MC1DN7
Rattus norvegicus (Norway rat)
DOID:0070336
  • arthrogryposis multiplex congenita-6
Mus musculus (house mouse)
DOID:0110928
  • nemaline myopathy 2
  • Aliases:
    • NEM2
    • congenital myopathy 2
    • nemaline myopathy 2, autosomal recessive
Mus musculus (house mouse)
DOID:0080443
  • developmental and epileptic encephalopathy 21
  • Aliases:
    • DEE21
    • early infantile epileptic encephalopathy 21
Mus musculus (house mouse)
DOID:2121
  • ectodermal dysplasia
  • Aliases:
    • Congenital ectodermal defect
    • Congenital ectodermal dysplasia
Rattus norvegicus (Norway rat)
DOID:0060773
  • cleft lip-palate-ectodermal dysplasia syndrome
  • Aliases:
    • CLPED1
    • Margarita type of ectodermal dysplasia
    • Zlotogora-Zilberman-Tenenbaum syndrome
    • cleft lip/palate-syndactyly-pili torti syndrome
    • syndactyly-ectodermal dysplasia-cleft/lip palate
Rattus norvegicus (Norway rat)
DOID:0060773
  • cleft lip-palate-ectodermal dysplasia syndrome
  • Aliases:
    • CLPED1
    • Margarita type of ectodermal dysplasia
    • Zlotogora-Zilberman-Tenenbaum syndrome
    • cleft lip/palate-syndactyly-pili torti syndrome
    • syndactyly-ectodermal dysplasia-cleft/lip palate
Mus musculus (house mouse)
DOID:0050477
  • Liddle syndrome
  • Aliases:
    • Liddle's syndrome
    • Pseudoaldosteronism
Mus musculus (house mouse)
DOID:0040089
  • autoimmune optic neuritis
Mus musculus (house mouse)
DOID:0110180
  • Charcot-Marie-Tooth disease axonal type 2CC
  • Aliases:
    • CMT2CC
    • Charcot-Marie-Tooth neuropathy type 2CC
Mus musculus (house mouse)
DOID:0050433
  • fatal familial insomnia
Mus musculus (house mouse)
DOID:0080294
  • Charcot-Marie-Tooth disease dominant intermediate G
Mus musculus (house mouse)
DOID:643
  • progressive multifocal leukoencephalopathy
Mus musculus (house mouse)
DOID:0110149
  • Charcot-Marie-Tooth disease type 1F
  • Aliases:
    • CMT1F
    • Charcot-Marie-Tooth neuropathy type 1F
Mus musculus (house mouse)
DOID:0110165
  • Charcot-Marie-Tooth disease type 2E
  • Aliases:
    • CMT2E
    • Charcot-Marie-Tooth neuropathy type 2E
    • autosomal dominant Charcot-Marie-Tooth disease type 2E
Mus musculus (house mouse)
DOID:11949
  • Creutzfeldt-Jakob disease
  • Aliases:
    • CJD
    • Creutzfeldt Jacob syndrome
    • Creutzfeldt Jakob disease
    • Creutzfeldt-Jacob disease
    • Jakob-Creutzfeldt disease
    • Subacute spongiform encephalopathy
    • Transmissible virus dementia
Rattus norvegicus (Norway rat)
DOID:0050433
  • fatal familial insomnia
Rattus norvegicus (Norway rat)
DOID:0080832
  • mild cognitive impairment
Rattus norvegicus (Norway rat)
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Last updated: December 9, 2024