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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 12526 - 12550 of 15957 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism Source
DOID:0080136
  • multiple mitochondrial dysfunctions syndrome 4
Homo sapiens (human)
DOID:0080135
  • multiple mitochondrial dysfunctions syndrome 3
  • Aliases:
    • IBA57 deficiency
Homo sapiens (human)
DOID:0080133
  • multiple mitochondrial dysfunctions syndrome 1
  • Aliases:
    • NFU1 deficiency
Homo sapiens (human)
DOID:0080133
  • multiple mitochondrial dysfunctions syndrome 1
  • Aliases:
    • NFU1 deficiency
Mus musculus (house mouse)
DOID:0080132
  • Sengers syndrome
  • Aliases:
    • mitochondrial DNA depletion syndrome 10
    • mitochondrial DNA depletion syndrome 10 (cardiomyopathic type)
Homo sapiens (human)
DOID:0080131
  • mitochondrial DNA depletion syndrome 13
  • Aliases:
    • FBXL4 deficiency
    • FBXL4-related encephalomyopathic mitochondrial DNA depletion syndrome
    • mitochondrial DNA depletion syndrome 13, encephalomyopathic type
Homo sapiens (human)
DOID:0080130
  • mitochondrial DNA depletion syndrome 12a
Rattus norvegicus (Norway rat)
DOID:0080130
  • mitochondrial DNA depletion syndrome 12a
Mus musculus (house mouse)
DOID:0080128
  • mitochondrial DNA depletion syndrome 9
  • Aliases:
    • fatal infantile lactic acidosis
Homo sapiens (human)
DOID:0080124
  • mitochondrial DNA depletion syndrome 5
  • Aliases:
    • succinate-CoA ligase deficiency
Homo sapiens (human)
DOID:0080124
  • mitochondrial DNA depletion syndrome 5
  • Aliases:
    • succinate-CoA ligase deficiency
Rattus norvegicus (Norway rat)
DOID:0080124
  • mitochondrial DNA depletion syndrome 5
  • Aliases:
    • succinate-CoA ligase deficiency
Mus musculus (house mouse)
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: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
Mus musculus (house mouse)
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
Homo sapiens (human)
DOID:0080119
  • mitochondrial DNA depletion syndrome 1
  • Aliases:
    • mitochondrial DNA depletion syndrome 1 (MNGIE type)
    • mitochondrial neurogastrointestinal encephalopathy syndrome, TYMP-related
Rattus norvegicus (Norway rat)
DOID:0080119
  • mitochondrial DNA depletion syndrome 1
  • Aliases:
    • mitochondrial DNA depletion syndrome 1 (MNGIE type)
    • mitochondrial neurogastrointestinal encephalopathy syndrome, TYMP-related
Homo sapiens (human)
DOID:0080119
  • mitochondrial DNA depletion syndrome 1
  • Aliases:
    • mitochondrial DNA depletion syndrome 1 (MNGIE type)
    • mitochondrial neurogastrointestinal encephalopathy syndrome, TYMP-related
Mus musculus (house mouse)
DOID:0080118
  • mitochondrial complex III deficiency nuclear type 9
Homo sapiens (human)
DOID:0080115
  • mitochondrial complex III deficiency nuclear type 6
Mus musculus (house mouse)
DOID:0080114
  • mitochondrial complex III deficiency nuclear type 5
Rattus norvegicus (Norway rat)
DOID:0080114
  • mitochondrial complex III deficiency nuclear type 5
Mus musculus (house mouse)
DOID:0080114
  • mitochondrial complex III deficiency nuclear type 5
Homo sapiens (human)
DOID:0080113
  • mitochondrial complex III deficiency nuclear type 4
Rattus norvegicus (Norway rat)
DOID:0080112
  • mitochondrial complex III deficiency nuclear type 3
Rattus norvegicus (Norway rat)
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Last updated: December 9, 2024