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 9151 - 9175 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0060604
  • ankyloglossia
  • Aliases:
    • tongue-tie
Homo sapiens (human)
DOID:2671
  • transitional cell carcinoma
  • Aliases:
    • transitional carcinoma
    • transitional cell tumor
    • urothelial cell carcinoma
Mus musculus (house mouse)
DOID:0060395
  • chromosome 15q24 deletion syndrome
  • Aliases:
    • 15q24 microdeletion syndrome
Saccharomyces cerevisiae S288C
DOID:5773
  • oral submucous fibrosis
  • Aliases:
    • Oral cavity Submucous Fibrosis
    • Oral submucosal fibrosis
    • Oral submucosal fibrosis, including of tongue
Homo sapiens (human)
DOID:0111969
  • immunodeficiency 39
  • Aliases:
    • IMD39
Homo sapiens (human)
DOID:0090113
  • RIDDLE syndrome
  • Aliases:
    • RNF168 deficiency
    • Radiosensitivity-immunodeficiency-dysmorphic features-learning difficulties syndrome
Homo sapiens (human)
DOID:8544
  • chronic fatigue syndrome
  • Aliases:
    • CFS
    • Myalgic encephalitis
    • Myalgic encephalomyelitis
    • Postviral fatigue syndrome
Saccharomyces cerevisiae S288C
DOID:13166
  • allergic bronchopulmonary aspergillosis
  • Aliases:
    • pulmonary aspergillus disease
Mus musculus (house mouse)
DOID:0050630
  • Aland Island eye disease
  • Aliases:
    • FORSIUS-ERIKSSON TYPE OCULAR ALBINISM
    • Forsius-Eriksson syndrome
Rattus norvegicus (Norway rat)
DOID:783
  • end stage renal disease
  • Aliases:
    • end stage renal failure
    • end-stage kidney disease
Xenopus tropicalis (tropical clawed frog)
DOID:687
  • hepatoblastoma
Mus musculus (house mouse)
DOID:0060284
  • paroxysmal nocturnal hemoglobinuria
Saccharomyces cerevisiae S288C
DOID:8927
  • learning disability
  • Aliases:
    • Academic skill disorder
    • learning disorder
Mus musculus (house mouse)
DOID:0110176
  • Charcot-Marie-Tooth disease axonal type 2X
  • Aliases:
    • Charcot-Marie-Tooth neuropathy type 2X
    • autosomal recessive axonal Charcot-Marie-Tooth disease type 2X
Homo sapiens (human)
DOID:0110721
  • neuronal ceroid lipofuscinosis 1
  • Aliases:
    • CLN1
    • neuronal ceroid lipofuscinosis 1 variable age of onset
Caenorhabditis elegans
DOID:13317
  • hyperinsulinemic hypoglycemia
  • Aliases:
    • Islet cell hyperplasia
    • nesidioblastosis
    • persistent hyperinsulinemia hypoglycemia of infancy
Homo sapiens (human)
DOID:0050588
  • muscular dystrophy-dystroglycanopathy type B1
  • Aliases:
    • CMD due to dystroglycanopathy
    • Muscular dystrophy-dystroglycanopathy congenital with impaired intellectual development B1
Saccharomyces cerevisiae S288C
DOID:4306
  • radiculopathy
  • Aliases:
    • pinched nerve
Rattus norvegicus (Norway rat)
DOID:0080952
  • AMED syndrome
  • Aliases:
    • AMEDS
Homo sapiens (human)
DOID:0060001
  • withdrawal disorder
Caenorhabditis elegans
DOID:0060856
  • right atrial isomerism
  • Aliases:
    • Ivemark syndrome
    • asplenia with cardiovascular anomalies
Caenorhabditis elegans
DOID:5410
  • pulmonary neuroendocrine tumor
Caenorhabditis elegans
DOID:6195
  • conjunctivitis
Caenorhabditis elegans
DOID:0110876
  • holoprosencephaly 7
  • Aliases:
    • HPE7
Mus musculus (house mouse)
DOID:0070065
  • autosomal dominant intellectual developmental disorder 35
  • Aliases:
    • MRD35
    • autosomal dominant mental retardation 35
    • autosomal dominant non-syndromic intellectual disability 35
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: February 17, 2025