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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 4901 - 4925 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:1222
  • cartilage disease
  • Aliases:
    • Cartilage disorder
    • Chondropathy
Xenopus laevis (African clawed frog)
DOID:799
  • varicose veins
  • Aliases:
    • Varix
    • Venous ectasia
    • Venous varices
    • varices
Homo sapiens (human)
DOID:0080414
  • developmental and epileptic encephalopathy 15
  • Aliases:
    • DEE15
    • early infantile epileptic encephalopathy 15
Mus musculus (house mouse)
DOID:0112313
  • brain small vessel disease
Caenorhabditis elegans
DOID:0080254
  • orofaciodigital syndrome XVI
Xenopus laevis (African clawed frog)
DOID:0110976
  • brachydactyly type E2
  • Aliases:
    • BDE2
Homo sapiens (human)
DOID:0070520
  • peeling skin syndrome 1
  • Aliases:
    • PSS1
    • generalized inflammatory peeling skin syndrome
    • inflammatory peeling skin syndrome
    • peeling skin syndrome type B
Homo sapiens (human)
DOID:1391
  • Norum disease
  • Aliases:
    • LECITHIN CHOLESTEROL ACYLTRANSFERASE DEFICIENCY
    • lecithin acyltransferase deficiency
Mus musculus (house mouse)
DOID:5138
  • leiomyomatosis
Homo sapiens (human)
DOID:9538
  • multiple myeloma
  • Aliases:
    • myeloma
Saccharomyces cerevisiae S288C
DOID:0060300
  • complement component 7 deficiency
Homo sapiens (human)
DOID:5199
  • ureteral obstruction
Drosophila melanogaster (fruit fly)
DOID:0111584
  • dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome
  • Aliases:
    • Malouf syndrome
    • Najjar syndrome
    • cardiogenital syndrome
    • cardiomyopathy eith primary testicular failure
    • congestive cardiomyopathy with hypergonadotropic hypogonadism
    • dilated cardiomyopathy with hypergonadotropic hypogonadism
    • dilated cardiomyopathy with premature ovarian failure
    • genital anomaly with cardiomyopathy
Mus musculus (house mouse)
DOID:0080589
  • Klippel-Feil syndrome 1
Rattus norvegicus (Norway rat)
DOID:0080319
  • X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia
  • Aliases:
    • XMEN
Homo sapiens (human)
DOID:12798
  • mucopolysaccharidosis
Homo sapiens (human)
DOID:0111933
  • phosphoglycerate kinase 1 deficiency
  • Aliases:
    • GSD due to phosphoglycerate kinase 1 deficiency
    • PGK1 deficiency
    • glycogen storage disease due to phosphoglycerate kinase 1 deficiency
    • glycogenosis due to phosphoglycerate kinase 1 deficiency
Caenorhabditis elegans
DOID:0060307
  • autosomal dominant intellectual developmental disorder
  • Aliases:
    • autosomal dominant mental retardation
    • autosomal dominant non-syndromic mental retardation
Caenorhabditis elegans
DOID:1270
  • hereditary hemorrhagic telangiectasia
  • Aliases:
    • Osler hemorrhagic telangiectasia syndrome
    • Osler-Weber-Rendu disease
    • Rendu-Osler-Weber disease
Xenopus laevis (African clawed frog)
DOID:11569
  • neurocirculatory asthenia
  • Aliases:
    • Cardiovascular malfunction arising from mental factors
    • Cardiovascular neurosis
    • Da Costa's syndrome
    • Krishaber's disease
Mus musculus (house mouse)
DOID:5199
  • ureteral obstruction
Caenorhabditis elegans
DOID:0110541
  • autosomal dominant nonsyndromic deafness 1
  • Aliases:
    • DFNA1
    • Konigsmark syndrome
    • LFHL1
    • autosomal dominant deafness 1
    • autosomal dominant deafness 1, with or without thrombocytopenia
    • hereditary low frequency hearing loss 1
Homo sapiens (human)
DOID:0090078
  • hypogonadotropic hypogonadism 7 with or without anosmia
Drosophila melanogaster (fruit fly)
DOID:10754
  • otitis media
Mus musculus (house mouse)
DOID:0081188
  • autosomal recessive intellectual developmental disorder 14
Rattus norvegicus (Norway rat)
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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