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 3751 - 3775 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0060643
  • primary sclerosing cholangitis
Drosophila melanogaster (fruit fly)
DOID:799
  • varicose veins
  • Aliases:
    • Varix
    • Venous ectasia
    • Venous varices
    • varices
Mus musculus (house mouse)
DOID:3082
  • interstitial lung disease
  • Aliases:
    • ILD
Danio rerio (zebrafish)
DOID:0070538
  • syndromic X-linked intellectual developmental disorder bain type
  • Aliases:
    • HNRNPH2-RNDD
    • HNRNPH2-related neurodevelopmental disorder
    • MRXSB
    • Mental Retardation, X-linked, Syndrome, Bain Type
Mus musculus (house mouse)
DOID:10825
  • essential hypertension
  • Aliases:
    • idiopathic hypertension
    • primary hypertension
Xenopus laevis (African clawed frog)
DOID:0080433
  • developmental and epileptic encephalopathy 51
  • Aliases:
    • DEE51
    • early infantile epileptic encephalopathy 51
Homo sapiens (human)
DOID:0050861
  • colorectal adenocarcinoma
Drosophila melanogaster (fruit fly)
DOID:0070525
  • peeling skin syndrome 6
  • Aliases:
    • PSS6
Homo sapiens (human)
DOID:9268
  • glycine encephalopathy
  • Aliases:
    • Non-ketotic hyperglycinemia
    • nonketotic hyperglycinemia
Rattus norvegicus (Norway rat)
DOID:0111498
  • combined oxidative phosphorylation deficiency 22
  • Aliases:
    • COXPD22
Rattus norvegicus (Norway rat)
DOID:14717
  • centronuclear myopathy
  • Aliases:
    • myotubular myopathy
Mus musculus (house mouse)
DOID:13207
  • proliferative diabetic retinopathy
  • Aliases:
    • PDR
Homo sapiens (human)
DOID:4549
  • extraskeletal myxoid chondrosarcoma
  • Aliases:
    • Myxoid extraosseous chondrosarcoma
    • extraosseous chondrosarcoma
Homo sapiens (human)
DOID:0110110
  • atrial heart septal defect 5
  • Aliases:
    • ASD5
    • atrial septal defect 5
Homo sapiens (human)
DOID:0080672
  • fibrochondrogenesis 1
Rattus norvegicus (Norway rat)
DOID:1024
  • leprosy
Caenorhabditis elegans
DOID:0050990
  • episodic ataxia type 2
Rattus norvegicus (Norway rat)
DOID:0111668
  • Kohlschutter-Tonz syndrome
  • Aliases:
    • KTZS
    • Kohlschutter's syndrome
    • amelocerebrohypohidrotic syndrome
    • epilepsy and yellow teeth
    • epilepsy dementia amelogenesis imperfecta
    • epilepsy-dementia-amelogenesis imperfecta syndrome
Rattus norvegicus (Norway rat)
DOID:0060868
  • leukoencephalopathy with vanishing white matter
  • Aliases:
    • CACH
    • CACH/VWM
    • childhood ataxia with central nervous system hypomyelination
    • vanishing white matter leukodystrophy
Homo sapiens (human)
DOID:231
  • motor neuron disease
Rattus norvegicus (Norway rat)
DOID:12556
  • acute kidney tubular necrosis
  • Aliases:
    • ATN - acute tubular necrosis
    • acute renal Failure with tubular necrosis
    • acute renal failure with lesion of tubular necrosis
    • acute tubular necrosis
    • acute tubule necrosis
Danio rerio (zebrafish)
DOID:0080059
  • autosomal recessive spinocerebellar ataxia 7
  • Aliases:
    • SCAR7
Mus musculus (house mouse)
DOID:0112147
  • retinitis pigmentosa 90
  • Aliases:
    • RP90
Rattus norvegicus (Norway rat)
DOID:11678
  • onchocerciasis
  • Aliases:
    • Infection by Onchocerca volvulus
    • Onchocerca volvulus infection
    • volvulosis
Rattus norvegicus (Norway rat)
DOID:0060571
  • Ritscher-Schinzel syndrome 1
Homo sapiens (human)

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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