GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources July 29, 2024
DisGeNET July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 4776 - 4800 of 7942 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism
DOID:14735
  • hereditary angioedema
  • Aliases:
    • HANE
    • Hereditary angioneurotic edema
Danio rerio (zebrafish)
DOID:1474
  • aggressive periodontitis
  • Aliases:
    • juvenile periodontitis
Homo sapiens (human)
DOID:14748
  • Sotos syndrome
  • Aliases:
    • cerebral gigantism
Homo sapiens (human)
DOID:14749
  • methylmalonic acidemia
  • Aliases:
    • methylmalonic aciduria
Homo sapiens (human)
DOID:1475
  • lymphangioma
  • Aliases:
    • Congenital lymphangioma
    • benign lymphangioma
Homo sapiens (human)
DOID:14753
  • isovaleric acidemia
  • Aliases:
    • Isovaleryl-CoA dehydrogenase deficiency
    • isovaleric acid CoA dehydrogenase deficiency
    • isovaleric aciduria
Homo sapiens (human)
DOID:14755
  • argininosuccinic aciduria
  • Aliases:
    • Argininosuccinate lyase deficiency
    • argininosuccinic acidemia
    • arginosuccinase deficiency
    • deficiency of argininosuccinate lyase
Homo sapiens (human)
DOID:14757
  • Ehlers-Danlos syndrome hypermobility type
  • Aliases:
    • Ehlers-Danlos syndrome, type 3
    • type III Ehlers-Danlos syndrome
Homo sapiens (human)
DOID:14761
  • Greig cephalopolysyndactyly syndrome
  • Aliases:
    • polysyndactyly with peculiars skull shape
Homo sapiens (human)
DOID:14764
  • Larsen syndrome
  • Aliases:
    • dominant larsen syndrome
Homo sapiens (human)
DOID:14766
  • renal agenesis
  • Aliases:
    • hereditary renal aplasia
    • hereditary urogenital adysplasia
    • renal adysplasia
    • renal aplasia
Homo sapiens (human)
DOID:14768
  • Saethre-Chotzen syndrome
Homo sapiens (human)
DOID:14773
  • cartilage-hair hypoplasia
  • Aliases:
    • CHH
    • McKusick type metaphyseal chondrodysplasia
    • Metaphyseal chondrodysplasia, McKusick type
Homo sapiens (human)
DOID:14775
  • brittle cornea syndrome 1
  • Aliases:
    • type VIB Ehlers-Danlos syndrome
Homo sapiens (human)
DOID:14777
  • benign familial neonatal epilepsy
  • Aliases:
    • familial neonatal seizures
Homo sapiens (human)
DOID:14784
  • olivopontocerebellar atrophy
  • Aliases:
    • Dejerine-Thomas syndrome
    • Thomas' syndrome
    • WADIA-SWAMI SYNDROME
Homo sapiens (human)
DOID:14789
  • spondyloepiphyseal dysplasia congenita
  • Aliases:
    • Late Spondyloepiphyseal Dysplasia
Homo sapiens (human)
DOID:14791
  • Leber congenital amaurosis
  • Aliases:
    • LCA
    • Leber's amaurosis
    • Leber's congenital amaurosis
    • Leber's disease
Homo sapiens (human)
DOID:14793
  • hypohidrotic ectodermal dysplasia
Homo sapiens (human)
DOID:14796
  • Dubowitz syndrome
  • Aliases:
    • Dubowitz's syndrome
Homo sapiens (human)
DOID:1485
  • cystic fibrosis
  • Aliases:
    • CF
    • mucoviscidosis
Homo sapiens (human)
DOID:1485
  • cystic fibrosis
  • Aliases:
    • CF
    • mucoviscidosis
Saccharomyces cerevisiae S288C
DOID:1485
  • cystic fibrosis
  • Aliases:
    • CF
    • mucoviscidosis
Drosophila melanogaster (fruit fly)
DOID:1485
  • cystic fibrosis
  • Aliases:
    • CF
    • mucoviscidosis
Rattus norvegicus (Norway rat)
DOID:1485
  • cystic fibrosis
  • Aliases:
    • CF
    • mucoviscidosis
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: August 19, 2024