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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 7101 - 7125 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
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
Mus musculus (house mouse)
DOID:0081290
  • Antley-Bixler syndrome without disordered steroidogenesis
Homo sapiens (human)
DOID:10787
  • premature menopause
  • Aliases:
    • Menopause - premature
    • Menopause praecox
Caenorhabditis elegans
DOID:0080520
  • Tn polyagglutination syndrome
  • Aliases:
    • galactosyltransferase deficiency
Drosophila melanogaster (fruit fly)
DOID:0080079
  • nonsyndromic congenital nail disorder 1
  • Aliases:
    • nonsyndromic congenital nail disorder 10
    • twenty-nail dystrophy
Homo sapiens (human)
DOID:10825
  • essential hypertension
  • Aliases:
    • idiopathic hypertension
    • primary hypertension
Drosophila melanogaster (fruit fly)
DOID:0080046
  • Stickler syndrome
Homo sapiens (human)
DOID:0060546
  • Hermansky-Pudlak syndrome 8
Homo sapiens (human)
DOID:2755
  • Mycobacterium avium complex disease
  • Aliases:
    • Infection due to Mycobacterium intracellulare
    • MAC disease
    • Mycobacterium Avium Infection
    • Mycobacterium avium Complex
Mus musculus (house mouse)
DOID:0080572
  • congenital disorder of glycosylation Iw
  • Aliases:
    • congenital disorder of glycosylation 1w
Danio rerio (zebrafish)
DOID:0110798
  • hereditary spastic paraplegia 46
  • Aliases:
    • SPG46
    • autosomal recessive spastic paraplegia 46
    • autosomal recessive spastic paraplegia type 46
Drosophila melanogaster (fruit fly)
DOID:0070222
  • progressive familial intrahepatic cholestasis 2
  • Aliases:
    • BSEP deficiency
    • PFIC2
Mus musculus (house mouse)
DOID:2468
  • psychotic disorder
  • Aliases:
    • mental or behavioural disorder
Mus musculus (house mouse)
DOID:0080589
  • Klippel-Feil syndrome 1
Homo sapiens (human)
DOID:0070037
  • autosomal dominant intellectual developmental disorder 7
  • Aliases:
    • DYRK1A syndrome
    • MRD7
    • autosomal dominant mental retardation 7
    • autosomal dominant non-syndromic intellectual disability 7
Homo sapiens (human)
DOID:0111198
  • autosomal dominant distal hereditary motor neuronopathy
  • Aliases:
    • autosomal dominant dHMN
    • autosomal dominant distal hereditary motor neuropathy
    • autosomal dominant distal spinal muscular atrophy
Homo sapiens (human)
DOID:14500
  • fucosidosis
  • Aliases:
    • A-fucosidase deficiency
    • alpha fucosidase deficiency
Mus musculus (house mouse)
DOID:0050883
  • infantile cerebellar-retinal degeneration
Saccharomyces cerevisiae S288C
DOID:0111412
  • exudative vitreoretinopathy 1
  • Aliases:
    • EVR1
Rattus norvegicus (Norway rat)
DOID:12401
  • intermittent explosive disorder
  • Aliases:
    • explosive personality disorder
Mus musculus (house mouse)
DOID:0081102
  • familial gestational hyperthyroidism
Mus musculus (house mouse)
DOID:0070117
  • Meckel syndrome 3
  • Aliases:
    • MKS3
    • Meckel-Gruber syndrome, type 3
Mus musculus (house mouse)
DOID:0110645
  • long QT syndrome 2
  • Aliases:
    • LQT2
Xenopus tropicalis (tropical clawed frog)
DOID:2810
  • middle lobe syndrome
Homo sapiens (human)
DOID:9733
  • renal tuberculosis
  • Aliases:
    • Tuberculosis of kidney
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