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 7826 - 7850 of 7942 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism
DOID:0050467
  • erythrokeratodermia variabilis
  • Aliases:
    • Erythrokeratodermia Figurata Variabilis
    • Greither Disease
Homo sapiens (human)
DOID:0050466
  • Loeys-Dietz syndrome
Homo sapiens (human)
DOID:0050465
  • Muir-Torre syndrome
Homo sapiens (human)
DOID:0050464
  • Farber lipogranulomatosis
  • Aliases:
    • Farber disease
    • N-laurylsphingosine deacylase deficiency
    • acid ceramidase deficiency
Homo sapiens (human)
DOID:0050463
  • campomelic dysplasia
  • Aliases:
    • Acampomelic Campomelic Dysplasia
Homo sapiens (human)
DOID:0050462
  • Antley-Bixler syndrome with disordered steroidogenesis
  • Aliases:
    • trapezoidocephaly-synostosis syndrome
Homo sapiens (human)
DOID:0050461
  • aspartylglucosaminuria
  • Aliases:
    • aspartylglucosaminidase deficiency
    • aspartylglycosaminuria
    • glycosylasparaginase deficiency
Homo sapiens (human)
DOID:0050460
  • Wolf-Hirschhorn syndrome
  • Aliases:
    • 4p deletion syndrome
    • PITT SYNDROME
    • Pitt-Rogers-Danks Syndrome
    • chromosome 4p16.3 deletion syndrome
Homo sapiens (human)
DOID:0050459
  • hyperphosphatemia
Homo sapiens (human)
DOID:0050458
  • juvenile myelomonocytic leukemia
Homo sapiens (human)
DOID:0050457
  • Sertoli cell-only syndrome
  • Aliases:
    • DEL CASTILLO SYNDROME
    • Germinal Cell Aplasia
Homo sapiens (human)
DOID:0050456
  • Buruli ulcer disease
  • Aliases:
    • Bairnsdale ulcer
    • Daintree ulcer
    • Mossman ulcer
    • Searl ulcer
    • Searle's ulcer
Homo sapiens (human)
DOID:0050454
  • periventricular nodular heterotopia
  • Aliases:
    • periventricular heterotopia
Homo sapiens (human)
DOID:0050453
  • lissencephaly
Xenopus laevis (African clawed frog)
DOID:0050453
  • lissencephaly
Drosophila melanogaster (fruit fly)
DOID:0050453
  • lissencephaly
Saccharomyces cerevisiae S288C
DOID:0050453
  • lissencephaly
Danio rerio (zebrafish)
DOID:0050453
  • lissencephaly
Homo sapiens (human)
DOID:0050453
  • lissencephaly
Mus musculus (house mouse)
DOID:0050453
  • lissencephaly
Xenopus tropicalis (tropical clawed frog)
DOID:0050453
  • lissencephaly
Rattus norvegicus (Norway rat)
DOID:0050452
  • mevalonic aciduria
  • Aliases:
    • Mevalonate Kinase Deficiency
Homo sapiens (human)
DOID:0050452
  • mevalonic aciduria
  • Aliases:
    • Mevalonate Kinase Deficiency
Rattus norvegicus (Norway rat)
DOID:0050452
  • mevalonic aciduria
  • Aliases:
    • Mevalonate Kinase Deficiency
Mus musculus (house mouse)
DOID:0050451
  • Brugada syndrome
  • Aliases:
    • Bangungut
    • Brugada type idiopathic ventricular fibrillation
    • Dream disease
    • Pokkuri death syndrome
    • SUNDS
    • sudden unexplained nocturnal death syndrome
Homo sapiens (human)

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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: August 19, 2024