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 2201 - 2225 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:2355
  • anemia
  • Aliases:
    • anaemia
Caenorhabditis elegans
DOID:2862
  • glucosephosphate dehydrogenase deficiency
  • Aliases:
    • Glucose-6-phosphate dehydrogenase deficiency
    • deficiency of G-6PD
Caenorhabditis elegans
DOID:0050948
  • autosomal dominant hypophosphatemic rickets
Mus musculus (house mouse)
DOID:2942
  • bronchiolitis
Mus musculus (house mouse)
DOID:4440
  • seminoma
  • Aliases:
    • Seminoma, Pure
Danio rerio (zebrafish)
DOID:1040
  • chronic lymphocytic leukemia
  • Aliases:
    • B-cell chronic lymphocytic leukaemia
    • B-cell chronic lymphocytic leukemia
    • CLL
    • chronic lymphatic leukaemia
    • chronic lymphatic leukemia
    • chronic lymphocytic leukaemia
    • lymphoplasmacytic leukaemia
    • lymphoplasmacytic leukemia
Xenopus tropicalis (tropical clawed frog)
DOID:9120
  • amyloidosis
  • Aliases:
    • amyloid disease
Rattus norvegicus (Norway rat)
DOID:0110033
  • autosomal recessive Alport syndrome
Mus musculus (house mouse)
DOID:750
  • peptic ulcer disease
  • Aliases:
    • acute peptic ulcer with hemorrhage
    • acute peptic ulcer with hemorrhage and perforation
    • acute peptic ulcer without hemorrhage and without perforation
Mus musculus (house mouse)
DOID:615
  • leukopenia
  • Aliases:
    • Leucopenia
Xenopus tropicalis (tropical clawed frog)
DOID:0111031
  • hemochromatosis type 5
  • Aliases:
    • FTH1-associated iron overload
    • FTH1-related iron overload
    • HFE5
Mus musculus (house mouse)
DOID:0070158
  • hereditary sensory neuropathy type 1E
  • Aliases:
    • HSN1E
    • hereditary sensory neuropathy type IE
Mus musculus (house mouse)
DOID:0111272
  • occipital horn syndrome
  • Aliases:
    • EDS IX
    • Ehlers-Danlos syndrome type 9
    • Ehlers-Danlos syndrome type IX
    • X-linked cutis laxa
Mus musculus (house mouse)
DOID:0060649
  • congenital hereditary endothelial dystrophy of cornea
  • Aliases:
    • CHED
Mus musculus (house mouse)
DOID:5453
  • pulmonary venoocclusive disease
  • Aliases:
    • pulmonary veno-occlusive disease
Drosophila melanogaster (fruit fly)
DOID:13810
  • familial hypercholesterolemia
  • Aliases:
    • Fredrickson type IIa hyperlipoproteinemia
    • Fredrickson type IIa lipidaemia
    • familial hyperbetalipoproteinaemia
    • familial hypercholesteremia
    • hyperbetalipoproteinemia
    • type II hyperlipidemia
Saccharomyces cerevisiae S288C
DOID:0060788
  • hypomyelinating leukodystrophy 10
  • Aliases:
    • HLD10
Homo sapiens (human)
DOID:0070038
  • autosomal dominant intellectual developmental disorder 8
  • Aliases:
    • MRD8
    • autosomal dominant mental retardation 8
    • autosomal dominant non-syndromic intellectual disability 8
Rattus norvegicus (Norway rat)
DOID:0110544
  • autosomal dominant nonsyndromic deafness 12
  • Aliases:
    • DFNA12
    • DFNA8
    • autosomal dominant deafness 12
    • autosomal dominant deafness 8
Mus musculus (house mouse)
DOID:3891
  • placental insufficiency
Rattus norvegicus (Norway rat)
DOID:0050565
  • autosomal recessive nonsyndromic deafness
Mus musculus (house mouse)
DOID:13949
  • interstitial cystitis
  • Aliases:
    • ulcerative cystitis
Caenorhabditis elegans
DOID:114
  • heart disease
Saccharomyces cerevisiae S288C
DOID:0060591
  • WHIM syndrome
  • Aliases:
    • WHIMS
    • warts, hypogammaglobulinemia, infections, and myelokathexis
    • warts-hypogammaglobulinemia-infections-myelokathexis syndrome
Mus musculus (house mouse)
DOID:0081123
  • X-linked mental retardation Gustavson type
  • Aliases:
    • mental retardation with optic atrophy, deafness and seizures
Homo sapiens (human)

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024