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 January 28, 2025
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 251 - 275 of 5716 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism Source
DOID:0050742
  • nicotine dependence
  • Aliases:
    • tobacco use disorder
Rattus norvegicus (Norway rat)
DOID:0050742
  • nicotine dependence
  • Aliases:
    • tobacco use disorder
Homo sapiens (human)
DOID:0050742
  • nicotine dependence
  • Aliases:
    • tobacco use disorder
Caenorhabditis elegans
DOID:0050744
  • anaplastic large cell lymphoma
Homo sapiens (human)
DOID:0050745
  • diffuse large B-cell lymphoma
  • Aliases:
    • DLBCL
Homo sapiens (human)
DOID:0050745
  • diffuse large B-cell lymphoma
  • Aliases:
    • DLBCL
Mus musculus (house mouse)
DOID:0050746
  • mantle cell lymphoma
Homo sapiens (human)
DOID:0050748
  • marginal zone lymphoma
  • Aliases:
    • marginal zone B-cell lymphoma
Homo sapiens (human)
DOID:0050749
  • peripheral T-cell lymphoma
Homo sapiens (human)
DOID:0050752
  • amyotrophic lateral sclerosis type 8
  • Aliases:
    • ALS8
    • amyotrophic lateral sclerosis 8
Homo sapiens (human)
DOID:0050753
  • cerebellar ataxia
Homo sapiens (human)
DOID:0050753
  • cerebellar ataxia
Mus musculus (house mouse)
DOID:0050754
  • ataxia with oculomotor apraxia type 1
Homo sapiens (human)
DOID:0050755
  • spinocerebellar ataxia with axonal neuropathy 2
  • Aliases:
    • AOA2
    • SCAN2
    • SCAR1
    • ataxia with oculomotor apraxia type 2
    • autosomal recessive spinocerebellar ataxia 1
    • autosomal recessive spinocerebellar ataxia with axonal neuropathy 2
    • spinocerebellar ataxia with axonal neuropathy type 2
Homo sapiens (human)
DOID:0050766
  • choreaacanthocytosis
  • Aliases:
    • Levine-Critchley syndrome
    • choreo-acanthocytosis
Homo sapiens (human)
DOID:0050766
  • choreaacanthocytosis
  • Aliases:
    • Levine-Critchley syndrome
    • choreo-acanthocytosis
Mus musculus (house mouse)
DOID:0050768
  • mitochondrial complex V (ATP synthase) deficiency nuclear type 1
  • Aliases:
    • MC5DN1
Homo sapiens (human)
DOID:0050770
  • polycystic liver disease
  • Aliases:
    • congenital cystic liver disease
    • congenital hepatic cyst
    • fibrocystic liver disease
Mus musculus (house mouse)
DOID:0050770
  • polycystic liver disease
  • Aliases:
    • congenital cystic liver disease
    • congenital hepatic cyst
    • fibrocystic liver disease
Homo sapiens (human)
DOID:0050771
  • pheochromocytoma
  • Aliases:
    • phaeochromocytoma
Homo sapiens (human)
DOID:0050771
  • pheochromocytoma
  • Aliases:
    • phaeochromocytoma
Mus musculus (house mouse)
DOID:0050771
  • pheochromocytoma
  • Aliases:
    • phaeochromocytoma
Rattus norvegicus (Norway rat)
DOID:0050773
  • paraganglioma
  • Aliases:
    • chemodectoma
    • glomus body tumor
Homo sapiens (human)
DOID:0050773
  • paraganglioma
  • Aliases:
    • chemodectoma
    • glomus body tumor
Rattus norvegicus (Norway rat)
DOID:0050774
  • rapadilino syndrome
Homo sapiens (human)

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Last updated: December 8, 2025