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 7626 - 7650 of 7942 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism
DOID:9266
  • cystinuria
Saccharomyces cerevisiae S288C
DOID:9266
  • cystinuria
Drosophila melanogaster (fruit fly)
DOID:9267
  • urea cycle disorder
  • Aliases:
    • disorder of metabolism of ornithine, citrulline, argininosuccinic acid, arginine and ammonia
    • disorder of urea cycle metabolism
    • urea cycle defect
Homo sapiens (human)
DOID:9268
  • glycine encephalopathy
  • Aliases:
    • Non-ketotic hyperglycinemia
    • nonketotic hyperglycinemia
Homo sapiens (human)
DOID:9269
  • maple syrup urine disease
  • Aliases:
    • Ketoacidaemia
    • branched chain ketoaciduria
Homo sapiens (human)
DOID:9270
  • alkaptonuria
  • Aliases:
    • Homogentisate 1,2-dioxygenase deficiency
    • alcaptonuria
Homo sapiens (human)
DOID:9271
  • ornithine carbamoyltransferase deficiency
  • Aliases:
    • deficiency of citrulline phosphorylase
    • ornithine transcarbamylase deficiency
Homo sapiens (human)
DOID:9273
  • citrullinemia
  • Aliases:
    • ASS deficiency
    • deficiency of citrulline-aspartate ligase
Homo sapiens (human)
DOID:9273
  • citrullinemia
  • Aliases:
    • ASS deficiency
    • deficiency of citrulline-aspartate ligase
Drosophila melanogaster (fruit fly)
DOID:9273
  • citrullinemia
  • Aliases:
    • ASS deficiency
    • deficiency of citrulline-aspartate ligase
Mus musculus (house mouse)
DOID:9274
  • hyperlysinemia
Homo sapiens (human)
DOID:9275
  • tyrosinemia
Homo sapiens (human)
DOID:9277
  • primary cerebellar degeneration
Homo sapiens (human)
DOID:9278
  • hyperargininemia
  • Aliases:
    • Arginase deficiency
    • argininemia
    • deficiency of canavanase
Homo sapiens (human)
DOID:9279
  • hyperhomocysteinemia
Caenorhabditis elegans
DOID:9279
  • hyperhomocysteinemia
Mus musculus (house mouse)
DOID:9279
  • hyperhomocysteinemia
Drosophila melanogaster (fruit fly)
DOID:9279
  • hyperhomocysteinemia
Saccharomyces cerevisiae S288C
DOID:9279
  • hyperhomocysteinemia
Homo sapiens (human)
DOID:9279
  • hyperhomocysteinemia
Rattus norvegicus (Norway rat)
DOID:9280
  • carbamoyl phosphate synthetase I deficiency disease
  • Aliases:
    • CPS I deficiency
Homo sapiens (human)
DOID:9281
  • phenylketonuria
  • Aliases:
    • Folling's disease
    • PKU
    • maternal phenylketonuria
    • phenylalaninemia
Drosophila melanogaster (fruit fly)
DOID:9281
  • phenylketonuria
  • Aliases:
    • Folling's disease
    • PKU
    • maternal phenylketonuria
    • phenylalaninemia
Mus musculus (house mouse)
DOID:9281
  • phenylketonuria
  • Aliases:
    • Folling's disease
    • PKU
    • maternal phenylketonuria
    • phenylalaninemia
Homo sapiens (human)
DOID:9281
  • phenylketonuria
  • Aliases:
    • Folling's disease
    • PKU
    • maternal phenylketonuria
    • phenylalaninemia
Rattus norvegicus (Norway rat)

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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