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 3101 - 3125 of 15957 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism Source
DOID:0111506
  • palmoplantar keratoderma-esophageal carcinoma syndrome
  • Aliases:
    • Bennion-Patterson syndrome
    • Howell-Evans syndrome
    • TOC
    • keratosis palmaris et plantaris with esophageal cancer
    • keratosis palmoplantaris-esophageal carcinoma syndrome
    • palmoplantar hyperkeratosis-esophageal carcinoma syndrome
    • palmoplantar keratoderma with esophageal cancer
    • tylosis with esophageal cancer
    • tylosis-oesophageal carcinoma syndrome
Homo sapiens (human)
DOID:0111506
  • palmoplantar keratoderma-esophageal carcinoma syndrome
  • Aliases:
    • Bennion-Patterson syndrome
    • Howell-Evans syndrome
    • TOC
    • keratosis palmaris et plantaris with esophageal cancer
    • keratosis palmoplantaris-esophageal carcinoma syndrome
    • palmoplantar hyperkeratosis-esophageal carcinoma syndrome
    • palmoplantar keratoderma with esophageal cancer
    • tylosis with esophageal cancer
    • tylosis-oesophageal carcinoma syndrome
Mus musculus (house mouse)
DOID:0111244
  • palmoplantar keratoderma and congenital alopecia 1
  • Aliases:
    • PPK-CA, Stevanovic type
    • PPKCA Stevanovic type
    • PPKCA1
    • autosomal dominant palmoplantar hyperkeratosis and congenital alopecia
    • autosomal dominant palmoplantar keratoderma and congenital alopecia
    • keratoderma-hypotrichosis-leukonychia totalis syndrome
    • palmoplantar keratoderma and congenital alopecia, Stevanovic type
Mus musculus (house mouse)
DOID:0050449
  • pachyonychia congenita
  • Aliases:
    • Jackson-Lawler Type Pachyonychia Congenita
    • Jadassohn-Lewandowsky Syndrome
    • PACHYONYCHIA CONGENITA, JADASSOHN-LEWANDOWSKY TYPE
    • Pachyonychia Congenita Type 1
Homo sapiens (human)
DOID:0081266
  • pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures
  • Aliases:
    • PAMDDFS
Homo sapiens (human)
DOID:5389
  • oxyphilic adenoma
  • Aliases:
    • Follicular adenoma, oxyphilic cell
    • Oncocytoma
Xenopus laevis (African clawed frog)
DOID:5389
  • oxyphilic adenoma
  • Aliases:
    • Follicular adenoma, oxyphilic cell
    • Oncocytoma
Danio rerio (zebrafish)
DOID:5389
  • oxyphilic adenoma
  • Aliases:
    • Follicular adenoma, oxyphilic cell
    • Oncocytoma
Mus musculus (house mouse)
DOID:5389
  • oxyphilic adenoma
  • Aliases:
    • Follicular adenoma, oxyphilic cell
    • Oncocytoma
Caenorhabditis elegans
DOID:5389
  • oxyphilic adenoma
  • Aliases:
    • Follicular adenoma, oxyphilic cell
    • Oncocytoma
Homo sapiens (human)
DOID:0081326
  • oxoglutarate dehydrogenase deficiency
  • Aliases:
    • Oxoglutaric aciduria
    • alpha-ketoglutarate dehydrogenase deficiency
Homo sapiens (human)
DOID:0081326
  • oxoglutarate dehydrogenase deficiency
  • Aliases:
    • Oxoglutaric aciduria
    • alpha-ketoglutarate dehydrogenase deficiency
Rattus norvegicus (Norway rat)
DOID:0081326
  • oxoglutarate dehydrogenase deficiency
  • Aliases:
    • Oxoglutaric aciduria
    • alpha-ketoglutarate dehydrogenase deficiency
Xenopus laevis (African clawed frog)
DOID:0081326
  • oxoglutarate dehydrogenase deficiency
  • Aliases:
    • Oxoglutaric aciduria
    • alpha-ketoglutarate dehydrogenase deficiency
Caenorhabditis elegans
DOID:0081326
  • oxoglutarate dehydrogenase deficiency
  • Aliases:
    • Oxoglutaric aciduria
    • alpha-ketoglutarate dehydrogenase deficiency
Mus musculus (house mouse)
DOID:654
  • overnutrition
Mus musculus (house mouse)
DOID:654
  • overnutrition
Rattus norvegicus (Norway rat)
DOID:654
  • overnutrition
Homo sapiens (human)
DOID:0111562
  • overhydrated hereditary stomatocytosis
  • Aliases:
    • OHS
    • potassium sodium disorder of erythrocyte
    • stomatocytosisIOHST
Mus musculus (house mouse)
DOID:0111562
  • overhydrated hereditary stomatocytosis
  • Aliases:
    • OHS
    • potassium sodium disorder of erythrocyte
    • stomatocytosisIOHST
Rattus norvegicus (Norway rat)
DOID:0111562
  • overhydrated hereditary stomatocytosis
  • Aliases:
    • OHS
    • potassium sodium disorder of erythrocyte
    • stomatocytosisIOHST
Homo sapiens (human)
DOID:0070355
  • overactive bladder syndrome
  • Aliases:
    • OAB
    • overactive bladder
    • urge syndrome
    • urgency-frequency syndrome
Rattus norvegicus (Norway rat)
DOID:0070355
  • overactive bladder syndrome
  • Aliases:
    • OAB
    • overactive bladder
    • urge syndrome
    • urgency-frequency syndrome
Xenopus laevis (African clawed frog)
DOID:0070355
  • overactive bladder syndrome
  • Aliases:
    • OAB
    • overactive bladder
    • urge syndrome
    • urgency-frequency syndrome
Mus musculus (house mouse)
DOID:0070355
  • overactive bladder syndrome
  • Aliases:
    • OAB
    • overactive bladder
    • urge syndrome
    • urgency-frequency syndrome
Caenorhabditis elegans

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Last updated: December 9, 2024