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 6651 - 6675 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▲
DOID:0110899
  • inflammatory bowel disease 28
  • Aliases:
    • IBD28
    • early onset autosomal recessive inflammatory bowel disease 28
Mus musculus (house mouse)
DOID:0110899
  • inflammatory bowel disease 28
  • Aliases:
    • IBD28
    • early onset autosomal recessive inflammatory bowel disease 28
Homo sapiens (human)
DOID:0110909
  • inflammatory bowel disease 25
  • Aliases:
    • IBD25
    • early onset autosomal recessive inflammatory bowel disease 25
Homo sapiens (human)
DOID:0110909
  • inflammatory bowel disease 25
  • Aliases:
    • IBD25
    • early onset autosomal recessive inflammatory bowel disease 25
Mus musculus (house mouse)
DOID:0110910
  • leukocyte adhesion deficiency 1
  • Aliases:
    • LAD1
    • LFA1 immunodeficiency
    • leukocyte adhesion deficiency type I
    • lymphocyte function-associated antigen 1 immunodeficiency
Caenorhabditis elegans
DOID:0110910
  • leukocyte adhesion deficiency 1
  • Aliases:
    • LAD1
    • LFA1 immunodeficiency
    • leukocyte adhesion deficiency type I
    • lymphocyte function-associated antigen 1 immunodeficiency
Drosophila melanogaster (fruit fly)
DOID:0110910
  • leukocyte adhesion deficiency 1
  • Aliases:
    • LAD1
    • LFA1 immunodeficiency
    • leukocyte adhesion deficiency type I
    • lymphocyte function-associated antigen 1 immunodeficiency
Homo sapiens (human)
DOID:0110910
  • leukocyte adhesion deficiency 1
  • Aliases:
    • LAD1
    • LFA1 immunodeficiency
    • leukocyte adhesion deficiency type I
    • lymphocyte function-associated antigen 1 immunodeficiency
Mus musculus (house mouse)
DOID:0110912
  • leukocyte adhesion deficiency 3
  • Aliases:
    • IADD
    • LAD1 variant
    • LAD1V
    • LAD3
    • integrin activation deficiency disease
    • leukocyte adhesion deficiency 1 variant
    • leukocyte adhesion deficiency type III
Homo sapiens (human)
DOID:0110913
  • adult hypophosphatasia
  • Aliases:
    • mild hypophosphatasia
Mus musculus (house mouse)
DOID:0110913
  • adult hypophosphatasia
  • Aliases:
    • mild hypophosphatasia
Rattus norvegicus (Norway rat)
DOID:0110913
  • adult hypophosphatasia
  • Aliases:
    • mild hypophosphatasia
Homo sapiens (human)
DOID:0110913
  • adult hypophosphatasia
  • Aliases:
    • mild hypophosphatasia
Saccharomyces cerevisiae S288C
DOID:0110914
  • infantile hypophosphatasia
  • Aliases:
    • Hops
    • phosphoethanolaminuria
Mus musculus (house mouse)
DOID:0110914
  • infantile hypophosphatasia
  • Aliases:
    • Hops
    • phosphoethanolaminuria
Rattus norvegicus (Norway rat)
DOID:0110914
  • infantile hypophosphatasia
  • Aliases:
    • Hops
    • phosphoethanolaminuria
Saccharomyces cerevisiae S288C
DOID:0110914
  • infantile hypophosphatasia
  • Aliases:
    • Hops
    • phosphoethanolaminuria
Homo sapiens (human)
DOID:0110915
  • childhood hypophosphatasia
Rattus norvegicus (Norway rat)
DOID:0110915
  • childhood hypophosphatasia
Mus musculus (house mouse)
DOID:0110915
  • childhood hypophosphatasia
Homo sapiens (human)
DOID:0110915
  • childhood hypophosphatasia
Saccharomyces cerevisiae S288C
DOID:0110916
  • hereditary spherocytosis type 1
  • Aliases:
    • HS1
    • SPH1
    • hereditary spherocytosis 1
Homo sapiens (human)
DOID:0110916
  • hereditary spherocytosis type 1
  • Aliases:
    • HS1
    • SPH1
    • hereditary spherocytosis 1
Mus musculus (house mouse)
DOID:0110917
  • hereditary spherocytosis type 2
  • Aliases:
    • HS2
    • SPH2
    • hereditary spherocytosis 2
Homo sapiens (human)
DOID:0110918
  • hereditary spherocytosis type 3
  • Aliases:
    • HS3
    • SPH3
    • hereditary spherocytosis 3
Homo sapiens (human)

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Last updated: December 9, 2024