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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 2401 - 2425 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism Source
DOID:4531
  • mucoepidermoid carcinoma
  • Aliases:
    • MEC
Rattus norvegicus (Norway rat)
DOID:9938
  • dacryocystitis
Rattus norvegicus (Norway rat)
DOID:11382
  • corneal neovascularization
Rattus norvegicus (Norway rat)
DOID:285
  • hairy cell leukemia
Rattus norvegicus (Norway rat)
DOID:0060645
  • chronic recurrent multifocal osteomyelitis
  • Aliases:
    • CRMO
    • chronic multifocal osteomyelitis
Rattus norvegicus (Norway rat)
DOID:8927
  • learning disability
  • Aliases:
    • Academic skill disorder
    • learning disorder
Rattus norvegicus (Norway rat)
DOID:0050854
  • Muckle-Wells syndrome
  • Aliases:
    • MWS
    • neutrophilic urticaria
Rattus norvegicus (Norway rat)
DOID:1532
  • pleural disease
  • Aliases:
    • disorder of pleura
    • non-neoplastic pleural disease
Rattus norvegicus (Norway rat)
DOID:8469
  • influenza
  • Aliases:
    • Influenza with other manifestations
    • flu
    • influenza with non-respiratory manifestation
Mus musculus (house mouse)
DOID:0060285
  • parietal foramina
  • Aliases:
    • Caitlin marks
    • enlarged parietal foramina
    • hereditary cranium bifidum
Homo sapiens (human)
DOID:0081046
  • frontonasal dysplasia 2
Homo sapiens (human)
DOID:0111496
  • combined oxidative phosphorylation deficiency 17
  • Aliases:
    • COXPD17
Homo sapiens (human)
DOID:0111753
  • infantile hypertrophic cardiomyopathy
Homo sapiens (human)
DOID:0110361
  • retinitis pigmentosa 75
  • Aliases:
    • RP75
Homo sapiens (human)
DOID:0110870
  • congenital stationary night blindness 1A
  • Aliases:
    • CSNB1A
    • NBMI
    • complete CSNB X-linked
    • congenital stationary night blindness 1A X-linked
    • congenital stationary night blindness with myopia
    • hemeralopia-myopia
    • myopia-night blindness
Homo sapiens (human)
DOID:0081153
  • common variable immunodeficiency 11
Mus musculus (house mouse)
DOID:0111982
  • immunodeficiency 56
  • Aliases:
    • IL21R immunodeficiency
    • IMD56
    • combined immunodeficiency due to IL21R deficiency
Mus musculus (house mouse)
DOID:0050816
  • urofacial syndrome
  • Aliases:
    • Ochoa syndrome
    • hydronephrosis with peculiar facial expression
Homo sapiens (human)
DOID:0110661
  • congenital myasthenic syndrome 20
  • Aliases:
    • CMS20
    • congenital myasthenic syndrome 20 presynaptic
Homo sapiens (human)
DOID:0111199
  • autosomal dominant distal hereditary motor neuronopathy 7
  • Aliases:
    • DHMN7A
    • DHMNVPy
    • HMN VIIA
    • HMN7A
    • Harper-Young myopath
    • dHMN7
    • distal hereditary motor neuronopathy type 7
    • distal hereditary motor neuropathy type VIIA
    • distal spinal muscular atrophy with vocal cord paralysis
    • distal spinal muscular atrophy with vocal cord paralysis type 7A
Homo sapiens (human)
DOID:0050985
  • spinocerebellar ataxia type 38
Homo sapiens (human)
DOID:1932
  • Angelman syndrome
  • Aliases:
    • happy puppet syndrome
    • puppetlike syndrome
Homo sapiens (human)
DOID:0111954
  • immunodeficiency 60
  • Aliases:
    • BACH2-related immunodeficiency and autoimmunity
    • BRIDA
    • IMD60
Homo sapiens (human)
DOID:0111813
  • syndactyly type 8
  • Aliases:
    • fusion of metacarpals 4 and 5
    • metacarpal 4-5 fusion
Rattus norvegicus (Norway rat)
DOID:4890
  • juvenile myoclonic epilepsy
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