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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 5576 - 5600 of 5716 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism Source
DOID:0050577
  • cranioectodermal dysplasia
  • Aliases:
    • Levin syndrome
    • Sensenbrenner syndrome
Saccharomyces cerevisiae S288C
DOID:0050576
  • Senior-Loken syndrome
  • Aliases:
    • Loken Senior syndrome
    • renal-retinal syndrome
Homo sapiens (human)
DOID:0050574
  • L-2-hydroxyglutaric aciduria
  • Aliases:
    • L-2-HYDROXYGLUTARIC ACIDEMIA
Homo sapiens (human)
DOID:0050573
  • 2-hydroxyglutaric aciduria
Homo sapiens (human)
DOID:0050572
  • cone-rod dystrophy
  • Aliases:
    • cone-rod retinal dystrophy
Homo sapiens (human)
DOID:0050572
  • cone-rod dystrophy
  • Aliases:
    • cone-rod retinal dystrophy
Danio rerio (zebrafish)
DOID:0050571
  • congenital disorder of glycosylation type II
Homo sapiens (human)
DOID:0050571
  • congenital disorder of glycosylation type II
Drosophila melanogaster (fruit fly)
DOID:0050570
  • congenital disorder of glycosylation type I
Mus musculus (house mouse)
DOID:0050570
  • congenital disorder of glycosylation type I
Danio rerio (zebrafish)
DOID:0050570
  • congenital disorder of glycosylation type I
Drosophila melanogaster (fruit fly)
DOID:0050570
  • congenital disorder of glycosylation type I
Homo sapiens (human)
DOID:0050570
  • congenital disorder of glycosylation type I
Saccharomyces cerevisiae S288C
DOID:0050569
  • Seckel syndrome
  • Aliases:
    • Harper's syndrome
    • Virchow-Seckel dwarfism
    • bird-headed dwarfism
    • microcephalic primordial dwarfism
Homo sapiens (human)
DOID:0050567
  • orofacial cleft
Homo sapiens (human)
DOID:0050565
  • autosomal recessive nonsyndromic deafness
Homo sapiens (human)
DOID:0050563
  • nonsyndromic deafness
  • Aliases:
    • nonsyndromic hearing loss
    • nonsyndromic hereditary hearing loss
Homo sapiens (human)
DOID:0050563
  • nonsyndromic deafness
  • Aliases:
    • nonsyndromic hearing loss
    • nonsyndromic hereditary hearing loss
Mus musculus (house mouse)
DOID:0050562
  • West syndrome
Homo sapiens (human)
DOID:0050561
  • Lennox-Gastaut syndrome
  • Aliases:
    • Lennox syndrome
Mus musculus (house mouse)
DOID:0050560
  • Walker-Warburg syndrome
  • Aliases:
    • HARD syndrome
    • cerebroocular dysplasia-muscular dystrophy syndrome
Danio rerio (zebrafish)
DOID:0050560
  • Walker-Warburg syndrome
  • Aliases:
    • HARD syndrome
    • cerebroocular dysplasia-muscular dystrophy syndrome
Saccharomyces cerevisiae S288C
DOID:0050560
  • Walker-Warburg syndrome
  • Aliases:
    • HARD syndrome
    • cerebroocular dysplasia-muscular dystrophy syndrome
Homo sapiens (human)
DOID:0050560
  • Walker-Warburg syndrome
  • Aliases:
    • HARD syndrome
    • cerebroocular dysplasia-muscular dystrophy syndrome
Drosophila melanogaster (fruit fly)
DOID:0050560
  • Walker-Warburg syndrome
  • Aliases:
    • HARD syndrome
    • cerebroocular dysplasia-muscular dystrophy syndrome
Mus musculus (house mouse)
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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