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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 January 28, 2025
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 1301 - 1325 of 5716 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism Source
DOID:0070580
  • spermatogenic failure 81
  • Aliases:
    • SPGF81
Homo sapiens (human)
DOID:0070583
  • spermatogenic failure 84
  • Aliases:
    • SPGF84
Homo sapiens (human)
DOID:0070584
  • spermatogenic failure 85
  • Aliases:
    • SPGF85
Homo sapiens (human)
DOID:0070586
  • spermatogenic failure 87
  • Aliases:
    • SPGF87
Homo sapiens (human)
DOID:0070587
  • spermatogenic failure 88
  • Aliases:
    • SPGF88
Homo sapiens (human)
DOID:0070588
  • spermatogenic failure 89
  • Aliases:
    • SPGF89
Homo sapiens (human)
DOID:0070595
  • X-linked spermatogenic failure 4
  • Aliases:
    • SPGFX4
Homo sapiens (human)
DOID:0070597
  • X-linked spermatogenic failure 6
  • Aliases:
    • SPGFX6
Homo sapiens (human)
DOID:0070599
  • X-linked spermatogenic failure 8
  • Aliases:
    • SPGFX8
Homo sapiens (human)
DOID:0070600
  • intellectual disability and myopathy syndrome
  • Aliases:
    • ABCC9-related intellectual disability and myopathy
    • AIMS
    • IDMYS
Homo sapiens (human)
DOID:0070601
  • autosomal dominant nonsyndromic deafness 37
  • Aliases:
    • DFNA37
    • autosomal dominant deafness 37
Homo sapiens (human)
DOID:0070602
  • autosomal dominant nonsyndromic deafness 80
  • Aliases:
    • DFNA80
    • autosomal dominant deafness 80
Homo sapiens (human)
DOID:0070605
  • autosomal dominant nonsyndromic deafness 85
  • Aliases:
    • DFNA85
    • autosomal dominant deafness 85
Homo sapiens (human)
DOID:0070606
  • autosomal dominant nonsyndromic deafness 87
  • Aliases:
    • DFNA87
    • autosomal dominant deafness 87
Homo sapiens (human)
DOID:0070609
  • autosomal dominant nonsyndromic deafness 83
  • Aliases:
    • DFNA83
    • autosomal dominant deafness 83
Homo sapiens (human)
DOID:0070610
  • autosomal dominant nonsyndromic deafness 86
  • Aliases:
    • DFNA86
    • autosomal dominant deafness 86
Homo sapiens (human)
DOID:0070611
  • autosomal dominant nonsyndromic deafness 88
  • Aliases:
    • DFNA88
    • autosomal dominant deafness 88
Homo sapiens (human)
DOID:0070613
  • familial renal glucosuria
  • Aliases:
    • FRG
    • SGLT2 deficiency
    • familial renal glycosuria
    • hereditary renal glycosuria
Homo sapiens (human)
DOID:0070615
  • autoinflammation, antibody deficiency, and immune dysregulation syndrome
  • Aliases:
    • APLAID
    • autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation
Homo sapiens (human)
DOID:0070616
  • glycine encephalopathy 1
  • Aliases:
    • GCE1
Homo sapiens (human)
DOID:0070618
  • rhabdoid tumor predisposition syndrome 1
  • Aliases:
    • RTPS1
Homo sapiens (human)
DOID:0070619
  • mitochondrial trifunctional protein deficiency 1
  • Aliases:
    • MTPD1
Homo sapiens (human)
DOID:0080000
  • muscular disease
Homo sapiens (human)
DOID:0080001
  • bone disease
Mus musculus (house mouse)
DOID:0080001
  • bone disease
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 8, 2025