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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 15401 - 15425 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism Source
DOID:0080570
  • congenital disorder of glycosylation It
  • Aliases:
    • congenital disorder of glycosylation 1t
Saccharomyces cerevisiae S288C
DOID:0070035
  • autosomal dominant intellectual developmental disorder 5
  • Aliases:
    • MRD5
    • autosomal dominant mental retardation 5
    • autosomal dominant non-syndromic intellectual disability 5
Saccharomyces cerevisiae S288C
DOID:0050830
  • peripheral artery disease
Saccharomyces cerevisiae S288C
DOID:9477
  • pulmonary embolism
  • Aliases:
    • pulmonary artery embolism
    • pulmonary embolus
Saccharomyces cerevisiae S288C
DOID:1936
  • atherosclerosis
Saccharomyces cerevisiae S288C
DOID:0080433
  • developmental and epileptic encephalopathy 51
  • Aliases:
    • DEE51
    • early infantile epileptic encephalopathy 51
Saccharomyces cerevisiae S288C
DOID:0080105
  • microcephaly and chorioretinopathy 1
Homo sapiens (human)
DOID:0111974
  • immunodeficiency 59
  • Aliases:
    • IMD59
    • granulocytopenia with immunoglobin abnormality
    • immunodeficiency 59 and hypoglycemia
Saccharomyces cerevisiae S288C
DOID:0112218
  • developmental and epileptic encephalopathy 83
  • Aliases:
    • DEE83
    • early infantile epileptic encephalopathy 83
Saccharomyces cerevisiae S288C
DOID:0060718
  • autosomal recessive congenital ichthyosis 9
  • Aliases:
    • ARCI9
Saccharomyces cerevisiae S288C
DOID:0111451
  • progressive myoclonus epilepsy 8
  • Aliases:
    • EMP8
    • PME type 8
    • progressive myoclonic epilepsy due to CERS1 deficiency
    • progressive myoclonus epilepsy type 8
Saccharomyces cerevisiae S288C
DOID:2476
  • hereditary spastic paraplegia
  • Aliases:
    • French settlement disease
    • Strumpell-Lorrain disease
    • familial spastic paraplegia
    • hereditary spastic paraparesis
Saccharomyces cerevisiae S288C
DOID:0060558
  • lethal congenital contracture syndrome
Saccharomyces cerevisiae S288C
DOID:4492
  • avian influenza
  • Aliases:
    • avian flu
    • bird flu
Saccharomyces cerevisiae S288C
DOID:14717
  • centronuclear myopathy
  • Aliases:
    • myotubular myopathy
Saccharomyces cerevisiae S288C
DOID:11166
  • Human papillomavirus infectious disease
  • Aliases:
    • HPV
Saccharomyces cerevisiae S288C
DOID:854
  • collagen disease
  • Aliases:
    • collagen disorder
Saccharomyces cerevisiae S288C
DOID:1827
  • idiopathic generalized epilepsy
  • Aliases:
    • Generalised epilepsy
Saccharomyces cerevisiae S288C
DOID:2975
  • cystic kidney disease
  • Aliases:
    • renal Cyst
Saccharomyces cerevisiae S288C
DOID:0080437
  • developmental and epileptic encephalopathy 31A
  • Aliases:
    • DEE31
    • DEE31A
    • developmental and epileptic encephalopathy 31
    • early infantile epileptic encephalopathy 31
Saccharomyces cerevisiae S288C
DOID:0070376
  • developmental and epileptic encephalopathy 31B
  • Aliases:
    • DEE31B
Saccharomyces cerevisiae S288C
DOID:0110197
  • Charcot-Marie-Tooth disease dominant intermediate B
  • Aliases:
    • CMTDI1
    • CMTDIB
    • Charcot-Marie-Tooth neuropathy dominant intermediate B
    • DI-CMTB
Saccharomyces cerevisiae S288C
DOID:11252
  • microcytic anemia
Saccharomyces cerevisiae S288C
DOID:0111223
  • centronuclear myopathy 1
  • Aliases:
    • CNM1
Saccharomyces cerevisiae S288C
DOID:0070053
  • autosomal dominant intellectual developmental disorder 23
  • Aliases:
    • MRD23
    • autosomal dominant mental retardation 23
    • autosomal dominant non-syndromic intellectual disability 23
Saccharomyces cerevisiae S288C
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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