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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 8401 - 8425 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism Source
DOID:10459
  • common cold
  • Aliases:
    • Acute viral rhinopharyngitis
    • Nasopharyngitis - acute
    • Nasopharyngitis, acute
    • acute coryza
    • acute nasopharyngitis
    • acute rhinitis
    • rhino-sinusitis
Homo sapiens (human)
DOID:0111013
  • cone-rod dystrophy 3
  • Aliases:
    • CORD3
Homo sapiens (human)
DOID:0110354
  • retinitis pigmentosa 19
  • Aliases:
    • RP19
Homo sapiens (human)
DOID:0110015
  • age related macular degeneration 2
  • Aliases:
    • ARMD2
Homo sapiens (human)
DOID:0050817
  • Stargardt disease
  • Aliases:
    • STARGARDT DISEASE 1
Homo sapiens (human)
DOID:8501
  • fundus dystrophy
  • Aliases:
    • Retinal Dystrophy
Homo sapiens (human)
DOID:0090048
  • dystonia 16
Mus musculus (house mouse)
DOID:0110704
  • hypotrichosis 7
  • Aliases:
    • Hypt7
    • Lah2
    • hypotrichosis, localized, autosomal recessive 2
    • total Mari type hypotrichosis,
Mus musculus (house mouse)
DOID:0111432
  • essential tremor 5
  • Aliases:
    • ETM5
    • hereditary essential tremor 5
Mus musculus (house mouse)
DOID:0060577
  • 3MC syndrome 3
Mus musculus (house mouse)
DOID:0112193
  • tetraamelia syndrome 2
  • Aliases:
    • TETAMS2
    • tetra-amelia with pulmonary hypoplasia
    • tetraamelia with pulmonary hypoplasia
Mus musculus (house mouse)
DOID:0081382
  • amyotrophic lateral sclerosis type 28
Mus musculus (house mouse)
DOID:0081297
  • oculopharyngodistal myopathy 1
Mus musculus (house mouse)
DOID:0081075
  • Marsili syndrome
  • Aliases:
    • congenital analgesia
    • congenital insensitivity to pain
Mus musculus (house mouse)
DOID:0070135
  • autosomal recessive cutis laxa type IA
  • Aliases:
    • ARCL1A
Mus musculus (house mouse)
DOID:0070136
  • autosomal dominant cutis laxa 2
  • Aliases:
    • ADCL2
Mus musculus (house mouse)
DOID:4972
  • myelodysplastic/myeloproliferative neoplasm
  • Aliases:
    • Myeloproliferative/Myelodysplastic syndromes
    • myelodysplastic myeloproliferative cancer
Mus musculus (house mouse)
DOID:0110063
  • amelogenesis imperfecta hypomaturation type 2A5
  • Aliases:
    • AI2A5
    • amelogenesis imperfecta hypomaturation type IIA5
    • amelogenesis imperfecta type IIA5
Mus musculus (house mouse)
DOID:0080960
  • amelogenesis imperfecta type 2A6
  • Aliases:
    • Amelogenesis imperfecta, hypomaturation type, IIA6
Mus musculus (house mouse)
DOID:0081327
  • neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures
  • Aliases:
    • NEDAMSS
Mus musculus (house mouse)
DOID:0110290
  • autosomal recessive limb-girdle muscular dystrophy type 2X
  • Aliases:
    • LGMD2X
    • muscular dystrophy, limb-girdle, type 2X
Mus musculus (house mouse)
DOID:2491
  • sensory peripheral neuropathy
  • Aliases:
    • peripheral Sensory Neuropathy
    • sensory neuropathy
Mus musculus (house mouse)
DOID:0111062
  • familial hypobetalipoproteinemia 1
  • Aliases:
    • FHBL1
Mus musculus (house mouse)
DOID:0111061
  • familial hypobetalipoproteinemia 2
  • Aliases:
    • FHBL2
    • combined familial hypolipidemia
Mus musculus (house mouse)
DOID:0080453
  • developmental and epileptic encephalopathy 25
  • Aliases:
    • DEE25
    • developmental and epileptic encephalopathy 25, with amelogenesis imperfecta
    • early infantile epileptic encephalopathy 25
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