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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 9151 - 9175 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism Source
DOID:13576
  • twin-to-twin transfusion syndrome
  • Aliases:
    • Fetal blood loss from fetal hemorrhage into co-twin
    • Fetal hemorrhage into co-twin
    • Twin to twin transfusion
    • Twin-to-twin blood transfer
Homo sapiens (human)
DOID:620
  • blood protein disease
  • Aliases:
    • blood protein disorder
Homo sapiens (human)
DOID:14089
  • root caries
  • Aliases:
    • Cementum caries
    • Dental caries of root surface
Homo sapiens (human)
DOID:2855
  • hyperthyroxinemia
Homo sapiens (human)
DOID:14525
  • Reye syndrome
  • Aliases:
    • Reye's syndrome
Homo sapiens (human)
DOID:6271
  • gastric cardia adenocarcinoma
  • Aliases:
    • adenocarcinoma of Cardia of stomach
Homo sapiens (human)
DOID:11266
  • Hantavirus hemorrhagic fever with renal syndrome
  • Aliases:
    • HFRS
    • Hemorrhagic fever, Russian
    • Hemorrhagic nephrosonephritis
    • Puumala virus nephropathy
Homo sapiens (human)
DOID:8924
  • autoimmune thrombocytopenic purpura
  • Aliases:
    • Immune thrombocytopenic purpura
    • idiopathic thrombocytopenic purpura
    • primary thrombocytopenic purpura
Homo sapiens (human)
DOID:0080737
  • Ehlers-Danlos syndrome musculocontractural type 2
Mus musculus (house mouse)
DOID:0110862
  • congenital stationary night blindness autosomal dominant 1
  • Aliases:
    • CSNBAD1
    • rhodopsin-related congenital stationary night blindness
Mus musculus (house mouse)
DOID:0110372
  • retinitis pigmentosa 4
  • Aliases:
    • RP4
Mus musculus (house mouse)
DOID:8499
  • night blindness
  • Aliases:
    • nyctalopia
Mus musculus (house mouse)
DOID:0081229
  • autosomal recessive intellectual developmental disorder 68
Mus musculus (house mouse)
DOID:0112243
  • congenital symmetric circumferential skin creases 2
  • Aliases:
    • CSCSC2
Mus musculus (house mouse)
DOID:0070004
  • myeloid neoplasm
Homo sapiens (human)
DOID:0081179
  • autosomal recessive intellectual developmental disorder 3
Mus musculus (house mouse)
DOID:0081301
  • intellectual developmental disorder with ocular anomalies and distinctive facial features
  • Aliases:
    • IDDOF
    • MTSS2-related neurodevelopmental disorder
Mus musculus (house mouse)
DOID:0110728
  • neuronal ceroid lipofuscinosis 5
  • Aliases:
    • CLN5
    • neuronal ceroid lipofuscinosis 5 variable age of onset
Mus musculus (house mouse)
DOID:0060358
  • multiple acyl-CoA dehydrogenase deficiency
  • Aliases:
    • MAD deficiency
    • MADD
    • electron transfer flavoprotein deficiency
    • electron transfer flavoprotein ubiquinone oxidoreductase deficiency
    • glutaric acidemia type 2
    • glutaric aciduria type 2
Homo sapiens (human)
DOID:0111225
  • centronuclear myopathy X-linked
  • Aliases:
    • CNMX
    • MTM1
    • X-linked myotubular myopathy
    • XLCNM
    • XLMTM
    • myotubular myopathy 1
Mus musculus (house mouse)
DOID:8029
  • sporadic breast cancer
Homo sapiens (human)
DOID:0110659
  • congenital myasthenic syndrome 7
  • Aliases:
    • CMS7
    • congenital myasthenic syndrome 7 presynaptic
Mus musculus (house mouse)
DOID:439
  • neuromuscular junction disease
Mus musculus (house mouse)
DOID:0112035
  • non-syndromic X-linked intellectual disability 96
  • Aliases:
    • MRX96
    • X-linked mental retardation 96
Mus musculus (house mouse)
DOID:0060894
  • early-onset Parkinson's disease
  • Aliases:
    • early-onset Parkinson disease
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 9, 2024