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 751 - 775 of 7942 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism
DOID:0060318
  • acute promyelocytic leukemia
  • Aliases:
    • acute myeloblastic leukaemia type 3
    • acute myeloblastic leukemia type 3
    • acute myeloid leukaemia M3
    • acute myeloid leukemia M3
    • acute promyelocytic leukaemia
Mus musculus (house mouse)
DOID:0060318
  • acute promyelocytic leukemia
  • Aliases:
    • acute myeloblastic leukaemia type 3
    • acute myeloblastic leukemia type 3
    • acute myeloid leukaemia M3
    • acute myeloid leukemia M3
    • acute promyelocytic leukaemia
Homo sapiens (human)
DOID:0060318
  • acute promyelocytic leukemia
  • Aliases:
    • acute myeloblastic leukaemia type 3
    • acute myeloblastic leukemia type 3
    • acute myeloid leukaemia M3
    • acute myeloid leukemia M3
    • acute promyelocytic leukaemia
Rattus norvegicus (Norway rat)
DOID:0060319
  • cardiac arrest
  • Aliases:
    • cardiopulmonary arrest
    • circulatory arrest
Homo sapiens (human)
DOID:0060319
  • cardiac arrest
  • Aliases:
    • cardiopulmonary arrest
    • circulatory arrest
Rattus norvegicus (Norway rat)
DOID:0060319
  • cardiac arrest
  • Aliases:
    • cardiopulmonary arrest
    • circulatory arrest
Mus musculus (house mouse)
DOID:0060320
  • inguinal hernia
Homo sapiens (human)
DOID:0060321
  • umbilical hernia
Homo sapiens (human)
DOID:0060322
  • mastoiditis
Drosophila melanogaster (fruit fly)
DOID:0060322
  • mastoiditis
Mus musculus (house mouse)
DOID:0060322
  • mastoiditis
Homo sapiens (human)
DOID:0060322
  • mastoiditis
Rattus norvegicus (Norway rat)
DOID:0060326
  • myelomeningocele
Homo sapiens (human)
DOID:0060327
  • omphalocele
  • Aliases:
    • omphalocoele
Homo sapiens (human)
DOID:0060330
  • Rapp-Hodgkin syndrome
  • Aliases:
    • RHS
    • anhidrotic ectodermal dysplasia with cleft lip/palate
    • ectodermal dysplasia syndrome, Rapp-Hodgkin type
    • ectodermal dysplasia, Rapp-Hodgkin type
Homo sapiens (human)
DOID:0060334
  • transient neonatal diabetes mellitus
Homo sapiens (human)
DOID:0060336
  • 3-methylglutaconic aciduria
Homo sapiens (human)
DOID:0060337
  • CEDNIK syndrome
  • Aliases:
    • cerebral dysgenesis, neuropathy, ichthyosis and keratoderma syndrome
Homo sapiens (human)
DOID:0060340
  • ciliopathy
Mus musculus (house mouse)
DOID:0060340
  • ciliopathy
Homo sapiens (human)
DOID:0060345
  • bacillary angiomatosis
Homo sapiens (human)
DOID:0060346
  • Native American myopathy
  • Aliases:
    • Bailey-Bloch congenital myopathy
    • congenital myopathy 13
Homo sapiens (human)
DOID:0060350
  • adenine phosphoribosyltransferase deficiency
  • Aliases:
    • 2,8-dihydroxyadenine urolithiasis
    • APRT deficiency
Drosophila melanogaster (fruit fly)
DOID:0060350
  • adenine phosphoribosyltransferase deficiency
  • Aliases:
    • 2,8-dihydroxyadenine urolithiasis
    • APRT deficiency
Rattus norvegicus (Norway rat)
DOID:0060350
  • adenine phosphoribosyltransferase deficiency
  • Aliases:
    • 2,8-dihydroxyadenine urolithiasis
    • APRT deficiency
Saccharomyces cerevisiae S288C

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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