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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 9526 - 9550 of 15957 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism Source
DOID:678
  • progressive supranuclear palsy
  • Aliases:
    • Steele-Richardson-Olszewski syndrome
    • progressive supranuclear ophthalmoplegia
Saccharomyces cerevisiae S288C
DOID:2671
  • transitional cell carcinoma
  • Aliases:
    • transitional carcinoma
    • transitional cell tumor
    • urothelial cell carcinoma
Saccharomyces cerevisiae S288C
DOID:3525
  • middle cerebral artery infarction
Saccharomyces cerevisiae S288C
DOID:2237
  • hepatitis
  • Aliases:
    • acute and subacute liver necrosis
    • acute hepatitis
    • acute/subac. necrosis of liver
    • animal hepatitis
    • chronic hepatitis
    • chronic persistent hepatitis
Saccharomyces cerevisiae S288C
DOID:5520
  • head and neck squamous cell carcinoma
  • Aliases:
    • carcinoma of the head and neck
    • squamous cell carcinoma of the head and neck
    • squamous cell carcinomas of head and neck
Saccharomyces cerevisiae S288C
DOID:2513
  • basal cell carcinoma
  • Aliases:
    • Basal cell cancer
    • Basal cell carcinoma of skin
    • Basal cell neoplasm
    • Basal cell tumor
    • Epithelioma basal cell
    • Rodent ulcer
    • malignant Basal cell neoplasm
    • malignant basal cell tumor
Saccharomyces cerevisiae S288C
DOID:12361
  • Graves' disease
  • Aliases:
    • Grave's disease
    • Graves disease
    • exophthalmic goiter
Saccharomyces cerevisiae S288C
DOID:0002116
  • pterygium
  • Aliases:
    • surfer's eye
Saccharomyces cerevisiae S288C
DOID:3314
  • angiomyolipoma
Saccharomyces cerevisiae S288C
DOID:1070
  • primary open angle glaucoma
  • Aliases:
    • chronic simple glaucoma
Saccharomyces cerevisiae S288C
DOID:0080240
  • non-syndromic X-linked intellectual disability 106
  • Aliases:
    • MRX106
    • X-linked mental retardation 106
Homo sapiens (human)
DOID:0111441
  • optic atrophy 1
  • Aliases:
    • OPA1
Homo sapiens (human)
DOID:0111340
  • dominant optic atrophy plus syndrome
  • Aliases:
    • DOA+
    • optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy
Homo sapiens (human)
DOID:0111580
  • Behr syndrome
  • Aliases:
    • Abortive cerebellar ataxia (BEHRS)
    • BEHRS
    • optic atrophy in early childhood, associated with ataxia, spasticity, mental retardation, and posterior column sensory loss
    • optic atrophy, infantile hereditary, Behr complicated form of
Homo sapiens (human)
DOID:0080336
  • mitochondrial DNA depletion syndrome 14
Homo sapiens (human)
DOID:0110004
  • 3-methylglutaconic aciduria type 3
  • Aliases:
    • 3-methylglutaconic aciduria type III
    • Costeff optic atrophy syndrome
    • Costeff syndrome
    • Iraqi-Jewish optic atrophy plus
    • MGA3
    • autosomal recessive optic atrophy plus syndrome
    • autosomal recessive optic atrophy type 3
    • infantile optic atrophy with chorea and spastic paraplegia
Homo sapiens (human)
DOID:0111433
  • optic atrophy 3
  • Aliases:
    • ADOAC
    • OPA3
    • autosomal dominant optic atrophy 3
    • autosomal dominant optic atrophy and cataract
    • autosomal dominant optic atrophy type 3
    • optic atrophy 3 with cataract
Homo sapiens (human)
DOID:0050679
  • blue cone monochromacy
Homo sapiens (human)
DOID:13910
  • red color blindness
  • Aliases:
    • Protan defect
    • Protanopia
Homo sapiens (human)
DOID:13909
  • red-green color blindness
  • Aliases:
    • Deutan defect
    • Deuteranopia
    • Reduced red-green discrimination
Homo sapiens (human)
DOID:0060203
  • amyotrophic lateral sclerosis type 12
  • Aliases:
    • ALS12
    • amyotrophic lateral sclerosis 12
Homo sapiens (human)
DOID:0081294
  • neuronal intranuclear inclusion disease
Homo sapiens (human)
DOID:0111976
  • immunodeficiency 9
  • Aliases:
    • CID due to ORAI1 deficiency
    • IMD9
    • combined immunodeficiency due to ORAI1 deficiency
    • immune dysfunction with T-cell inactivation due to calcium entry defect 1
Homo sapiens (human)
DOID:0080686
  • tubular aggregate myopathy 2
Homo sapiens (human)
DOID:0080512
  • Meier-Gorlin syndrome 1
Homo sapiens (human)
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Last updated: December 9, 2024