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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 4326 - 4350 of 4649 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▼
DOID:0060020
  • reticular dysgenesis
  • Aliases:
    • De Vaal disease
Homo sapiens (human)
DOID:0060019
  • coronin-1A deficiency
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:0060009
  • MHC class I deficiency
  • Aliases:
    • BLS, TYPE I
    • BLSI
    • HLA CLASS I DEFICIENCY
    • bare lymphocyte syndrome type I
Homo sapiens (human)
DOID:0060001
  • withdrawal disorder
Homo sapiens (human)
DOID:0060000
  • infective endocarditis
Homo sapiens (human)
DOID:0050998
  • nonprogressive cerebellar ataxia with mental retardation
Homo sapiens (human)
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:0050994
  • episodic ataxia type 6
Homo sapiens (human)
DOID:0050990
  • episodic ataxia type 2
Homo sapiens (human)
DOID:0050989
  • episodic ataxia type 1
Homo sapiens (human)
DOID:0050987
  • hypomyelinating leukoencephalopathy
Homo sapiens (human)
DOID:0050986
  • spinocerebellar ataxia type 40
Homo sapiens (human)
DOID:0050985
  • spinocerebellar ataxia type 38
Homo sapiens (human)
DOID:0050984
  • spinocerebellar ataxia type 37
Homo sapiens (human)
DOID:0050983
  • spinocerebellar ataxia type 36
Homo sapiens (human)
DOID:0050981
  • spinocerebellar ataxia type 34
Homo sapiens (human)
DOID:0050978
  • spinocerebellar ataxia type 29
Homo sapiens (human)
DOID:0050975
  • spinocerebellar ataxia type 26
Homo sapiens (human)
DOID:0050974
  • spinocerebellar ataxia type 25
Homo sapiens (human)
DOID:0050968
  • autosomal dominant cerebellar ataxia, deafness and narcolepsy
Homo sapiens (human)
DOID:0050967
  • spinocerebellar ataxia type 17
Homo sapiens (human)
DOID:0050965
  • spinocerebellar ataxia type 15
  • Aliases:
    • spinocerebellar ataxia type 16
Homo sapiens (human)
DOID:0050963
  • spinocerebellar ataxia type 13
Homo sapiens (human)
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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