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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 7251 - 7275 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0080562
  • congenital disorder of glycosylation Ij
  • Aliases:
    • Congenital disorder of glycosylation 1j
Saccharomyces cerevisiae S288C
DOID:0050697
  • chorioamnionitis
Homo sapiens (human)
DOID:0080118
  • mitochondrial complex III deficiency nuclear type 9
Homo sapiens (human)
DOID:3458
  • breast adenocarcinoma
  • Aliases:
    • Mammary adenocarcinoma
Mus musculus (house mouse)
DOID:3454
  • brain infarction
Mus musculus (house mouse)
DOID:9784
  • trichinosis
  • Aliases:
    • Trichinella spiralis infection
Caenorhabditis elegans
DOID:9775
  • diastolic heart failure
Xenopus tropicalis (tropical clawed frog)
DOID:0060250
  • idiopathic scoliosis
Mus musculus (house mouse)
DOID:0111404
  • Jalili syndrome
  • Aliases:
    • Cone rod dystrophy-amelogenesis imperfecta syndrome
    • cone-rod dystrophy and amelogenesis imperfecta
Mus musculus (house mouse)
DOID:0060697
  • hyperekplexia 2
  • Aliases:
    • HKPX2
Mus musculus (house mouse)
DOID:0060569
  • hypertrichotic osteochondrodysplasia Cantu type
  • Aliases:
    • Cantu syndrome
Rattus norvegicus (Norway rat)
DOID:0050836
  • focal dystonia
Homo sapiens (human)
DOID:653
  • purine-pyrimidine metabolic disorder
  • Aliases:
    • inborn errors of purine-pyrimidine metabolism
Mus musculus (house mouse)
DOID:0112184
  • thyroid dyshormonogenesis 5
  • Aliases:
    • TDH5
    • genetic defect in thyroid hormonogenesis 5
Caenorhabditis elegans
DOID:0060866
  • patterned macular dystrophy 1
  • Aliases:
    • MDPT1
    • butterfly-shaped pigmentary maculary dystrophy 1
Homo sapiens (human)
DOID:2843
  • long QT syndrome
  • Aliases:
    • LQT
    • long Q-T syndrome
Homo sapiens (human)
DOID:0110168
  • Charcot-Marie-Tooth disease type 2Y
  • Aliases:
    • CMT2 due to VCP mutation
    • CMT2Y
    • Charcot-Marie-Tooth neuropathy type 2Y
    • autosomal dominant Charcot-Marie-Tooth disease type 2 due to VCP mutation
    • autosomal dominant axonal Charcot-Marie-Tooth type 2Y
Homo sapiens (human)
DOID:8398
  • osteoarthritis
  • Aliases:
    • Osteoarthrosis and allied disorder
    • degenerative arthritis
    • degenerative joint disease
    • hypertrophic arthritis
    • osteoarthrosis
Xenopus tropicalis (tropical clawed frog)
DOID:4751
  • striatonigral degeneration
Homo sapiens (human)
DOID:4492
  • avian influenza
  • Aliases:
    • avian flu
    • bird flu
Mus musculus (house mouse)
DOID:0050462
  • Antley-Bixler syndrome with disordered steroidogenesis
  • Aliases:
    • trapezoidocephaly-synostosis syndrome
Homo sapiens (human)
DOID:11506
  • suppurative otitis media
  • Aliases:
    • Otitis media with effusion - purulent
    • Purulent otitis media
Rattus norvegicus (Norway rat)
DOID:4297
  • scimitar syndrome
  • Aliases:
    • Halasz syndrome
    • congenital venolobar syndrome
    • hypogenetic lung syndrome
    • mirror-image lung syndrome
    • pulmonary venolobar syndrome
    • total anomalous pulmonary venous return
    • vena cava bronchovascular syndrome
Danio rerio (zebrafish)
DOID:0110439
  • dilated cardiomyopathy 1P
  • Aliases:
    • CMD1P
Rattus norvegicus (Norway rat)
DOID:4661
  • multiple chemical sensitivity
  • Aliases:
    • 20th century disease
    • chemical AIDS
    • environmental illness
    • idiopathic environmental illness
    • total allergy 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 9, 2024