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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 4676 - 4700 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0110658
  • congenital myasthenic syndrome 15
  • Aliases:
    • CMS15
    • congenital myasthenic syndrome 15 without tubular aggregates
Saccharomyces cerevisiae S288C
DOID:0110255
  • cataract 5 multiple types
  • Aliases:
    • CTRCT5
Homo sapiens (human)
DOID:0050719
  • cerebral folate receptor alpha deficiency
  • Aliases:
    • Neurodegeneration due to cerebral folate transport deficiency
Homo sapiens (human)
DOID:0111753
  • infantile hypertrophic cardiomyopathy
Homo sapiens (human)
DOID:0110428
  • dilated cardiomyopathy 1AA
  • Aliases:
    • CMD1AA
    • dilated cardiomyopathy 1AA with or without left ventricular noncompaction
Homo sapiens (human)
DOID:0050456
  • Buruli ulcer disease
  • Aliases:
    • Bairnsdale ulcer
    • Daintree ulcer
    • Mossman ulcer
    • Searl ulcer
    • Searle's ulcer
Caenorhabditis elegans
DOID:4621
  • holoprosencephaly
  • Aliases:
    • Holoprosencephaly sequence
Mus musculus (house mouse)
DOID:0110079
  • Leber congenital amaurosis 8
  • Aliases:
    • LCA8
Mus musculus (house mouse)
DOID:0060577
  • 3MC syndrome 3
Xenopus tropicalis (tropical clawed frog)
DOID:0060850
  • annular pancreas
Mus musculus (house mouse)
DOID:0050663
  • Bethlem myopathy
  • Aliases:
    • benign congenital muscular dystrophy
Mus musculus (house mouse)
DOID:2223
  • platelet storage pool deficiency
  • Aliases:
    • Dense body defect
    • Platelet dense granule deficiency
    • Platelet storage pool defect
Mus musculus (house mouse)
DOID:0090045
  • childhood onset GLUT1 deficiency syndrome 2
Rattus norvegicus (Norway rat)
DOID:620
  • blood protein disease
  • Aliases:
    • blood protein disorder
Homo sapiens (human)
DOID:0060654
  • lethal congenital contracture syndrome 4
Homo sapiens (human)
DOID:12297
  • Vogt-Koyanagi-Harada disease
  • Aliases:
    • Harada's disease
    • Vogt-Koyanagi syndrome
    • uveomeningoencephalitic syndrome
Homo sapiens (human)
DOID:2799
  • bronchiolitis obliterans
  • Aliases:
    • Bronchiolitis exudativa
    • Bronchiolitis fibrosa obliterans
    • Obliterative bronchiolitis
Danio rerio (zebrafish)
DOID:8283
  • peritonitis
  • Aliases:
    • Retractile mesenteritis
    • acute generalized peritonitis
    • primary bacterial peritonitis
    • sclerosing mesenteritis
Caenorhabditis elegans
DOID:0080337
  • mitochondrial DNA depletion syndrome 15
Homo sapiens (human)
DOID:3620
  • central nervous system cancer
  • Aliases:
    • CNS neoplasm
    • central nervous system tumor
    • central nervous system tumors
    • malignant neoplasm of central nervous system
    • malignant tumor of CNS
    • neoplasm of central nervous system
Caenorhabditis elegans
DOID:0111453
  • 2-aminoadipic 2-oxoadipic aciduria
  • Aliases:
    • AMOXAD
    • alpha-aminoadipic aciduria
Danio rerio (zebrafish)
DOID:3328
  • temporal lobe epilepsy
  • Aliases:
    • epilepsy, temporal lobe
Danio rerio (zebrafish)
DOID:0111238
  • congenital muscular dystrophy-dystroglycanopathy type A13
  • Aliases:
    • MDDGA13
    • Walker-Warburg syndrome or muscle-eye-brain disease, B3GNT1-related
    • Walker-Warburg syndrome or muscle-eye-brain disease, B4GNT1-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A13
Homo sapiens (human)
DOID:0070309
  • absence epilepsy
Drosophila melanogaster (fruit fly)
DOID:11823
  • hepatorenal syndrome
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