GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources July 29, 2024
DisGeNET July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 6101 - 6125 of 7942 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism
DOID:9455
  • lipid storage disease
  • Aliases:
    • Lipoid storage diseas
    • inborn lipid storage disorder
    • lipoidosis
Homo sapiens (human)
DOID:3211
  • lysosomal storage disease
  • Aliases:
    • disorder of lysosomal enzyme
    • inborn lysosomal enzyme disorder
    • lysosomal storage metabolism disorder
Homo sapiens (human)
DOID:0060357
  • chylomicron retention disease
  • Aliases:
    • Anderson disease
    • CMRD
Homo sapiens (human)
DOID:13166
  • allergic bronchopulmonary aspergillosis
  • Aliases:
    • pulmonary aspergillus disease
Homo sapiens (human)
DOID:5212
  • congenital disorder of glycosylation
  • Aliases:
    • carbohydrate-deficient glycoprotein syndrome
Homo sapiens (human)
DOID:1949
  • cholecystitis
  • Aliases:
    • acute and chronic cholecystitis
    • acute cholecystitis
    • acute on chronic cholecystitis
    • chronic cholecystitis
Homo sapiens (human)
DOID:13922
  • eosinophilic esophagitis
Homo sapiens (human)
DOID:0050801
  • androgenic alopecia
  • Aliases:
    • alopecia androgenetica, male pattern baldness
    • androgenetic alopecia
Homo sapiens (human)
DOID:3744
  • cervical squamous cell carcinoma
  • Aliases:
    • squamous cell carcinoma of cervix
    • squamous cell carcinoma of the Cervix Uteri
Homo sapiens (human)
DOID:13189
  • gout
  • Aliases:
    • Articular gout
    • Gouty arthropathy
    • gouty arthritis
Homo sapiens (human)
DOID:0070352
  • stress-induced childhood-onset neurodegeneration with variable ataxia and seizures
  • Aliases:
    • CONDSIAS
Homo sapiens (human)
DOID:0060261
  • congenital ptosis
Homo sapiens (human)
DOID:0060260
  • ptosis
  • Aliases:
    • blepharoptosis
    • drooping eyelid
Homo sapiens (human)
DOID:2755
  • Mycobacterium avium complex disease
  • Aliases:
    • Infection due to Mycobacterium intracellulare
    • MAC disease
    • Mycobacterium Avium Infection
    • Mycobacterium avium Complex
Homo sapiens (human)
DOID:13608
  • biliary atresia
  • Aliases:
    • Atresia of bile duct
    • Congenital biliary atresia
    • biliary atresia, congenital
Homo sapiens (human)
DOID:1580
  • diffuse scleroderma
  • Aliases:
    • diffuse systemic sclerosis
    • systemic sclerosis, diffuse
Homo sapiens (human)
DOID:1206
  • Rett syndrome
  • Aliases:
    • Rett's disorder
    • cerebroatrophic hyperammonemia
Homo sapiens (human)
DOID:14791
  • Leber congenital amaurosis
  • Aliases:
    • LCA
    • Leber's amaurosis
    • Leber's congenital amaurosis
    • Leber's disease
Homo sapiens (human)
DOID:12271
  • aniridia
  • Aliases:
    • Aplasia of iris
    • isolated aniridia
Homo sapiens (human)
DOID:2855
  • hyperthyroxinemia
Homo sapiens (human)
DOID:0080952
  • AMED syndrome
  • Aliases:
    • AMEDS
Homo sapiens (human)
DOID:12450
  • pancytopenia
Homo sapiens (human)
DOID:13636
  • Fanconi anemia
  • Aliases:
    • Fanconi anaemia
    • Fanconi pancytopenia
    • Fanconi panmyelopathy
    • Fanconi's anaemia
    • Fanconi's anemia
Homo sapiens (human)
DOID:3168
  • squamous cell neoplasm
  • Aliases:
    • Epidermoid cell tumor
    • squamous cell tumor
Homo sapiens (human)
DOID:0050997
  • cerebellar ataxia, mental retardation and dysequlibrium syndrome
  • Aliases:
    • CAMRQ
    • Cerebellar Ataxia, Mental Retardation, and Dysequilibrium Syndrome 1 (CAMRQ1)
    • Uner Tan syndrome
    • VLDLR Cerebellar Hypoplasia
Homo sapiens (human)

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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: August 19, 2024