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 7376 - 7400 of 7942 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism
DOID:0060041
  • autism spectrum disorder
Caenorhabditis elegans
DOID:0060036
  • intrinsic cardiomyopathy
Drosophila melanogaster (fruit fly)
DOID:0060025
  • immunoglobulin alpha deficiency
  • Aliases:
    • IgA deficiency
    • gamma-A-globulin deficiency
Homo sapiens (human)
DOID:0060023
  • immunodeficiency with hyper IgM type 3
  • Aliases:
    • CD40 deficiency
    • HIGM3
    • hyper-IgM syndrome due to CD40 deficiency
    • type 3 hyper-IgM immunodeficiency
Homo sapiens (human)
DOID:0060022
  • CD40 ligand deficiency
  • Aliases:
    • HIGMX-1
    • X-linked hyper-IgM syndrome
Homo sapiens (human)
DOID:0060013
  • X-linked severe combined immunodeficiency
  • Aliases:
    • SCID-X1
    • XSCID
    • gamma chain deficiency
    • thymic epithelial hypoplasia
Homo sapiens (human)
DOID:0060010
  • Omenn syndrome
  • Aliases:
    • combined immunodeficiency with hypereosinophilia
Homo sapiens (human)
DOID:0060001
  • withdrawal disorder
Homo sapiens (human)
DOID:0060001
  • withdrawal disorder
Mus musculus (house mouse)
DOID:0060001
  • withdrawal disorder
Rattus norvegicus (Norway rat)
DOID:0060000
  • infective endocarditis
Homo sapiens (human)
DOID:0060000
  • infective endocarditis
Mus musculus (house mouse)
DOID:0050997
  • cerebellar ataxia, mental retardation and dysequlibrium syndrome
  • Aliases:
    • CAMRQ
    • Cerebellar Ataxia, Mental Retardation, and Dysequilibrium Syndrome 1 (CAMRQ1)
    • Uner Tan syndrome
    • VLDLR Cerebellar Hypoplasia
Homo sapiens (human)
DOID:0050990
  • episodic ataxia type 2
Homo sapiens (human)
DOID:0050989
  • episodic ataxia type 1
Homo sapiens (human)
DOID:0050985
  • spinocerebellar ataxia type 38
Homo sapiens (human)
DOID:0050981
  • spinocerebellar ataxia type 34
Homo sapiens (human)
DOID:0050980
  • spinocerebellar ataxia type 31
Homo sapiens (human)
DOID:0050967
  • spinocerebellar ataxia type 17
Homo sapiens (human)
DOID:0050959
  • spinocerebellar ataxia type 8
Homo sapiens (human)
DOID:0050958
  • spinocerebellar ataxia type 7
Homo sapiens (human)
DOID:0050956
  • spinocerebellar ataxia type 6
Homo sapiens (human)
DOID:0050955
  • spinocerebellar ataxia type 2
Homo sapiens (human)
DOID:0050954
  • spinocerebellar ataxia type 1
Homo sapiens (human)
DOID:0050951
  • hereditary ataxia
Homo sapiens (human)

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Last updated: August 19, 2024