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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 3301 - 3325 of 4649 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▼
DOID:0080726
  • Ehlers-Danlos syndrome classic type 2
Homo sapiens (human)
DOID:0080722
  • Kenny-Caffey syndrome type 1
Homo sapiens (human)
DOID:0080721
  • calvarial doughnut lesions with bone fragility
Homo sapiens (human)
DOID:0080719
  • congenital myopathy 6
  • Aliases:
    • inclusion body myopathy 3
    • proximal myopathy and ophthalmoplegia
Homo sapiens (human)
DOID:0080717
  • infantile liver failure syndrome 1
Homo sapiens (human)
DOID:0080716
  • infantile liver failure syndrome
Homo sapiens (human)
DOID:0080698
  • Teebi hypertelorism syndrome 1
  • Aliases:
    • Opitz GBBB syndrome type II
    • SPECC1L-related hypertelorism syndrome
    • Teebi hypertelorism syndrome-1
Homo sapiens (human)
DOID:0080697
  • Opitz GBBB syndrome
  • Aliases:
    • Opitz G/BBB Syndrome
    • Opitz GBBB syndrome type I
Homo sapiens (human)
DOID:0080696
  • Winchester syndrome
Homo sapiens (human)
DOID:0080695
  • Burn-McKeown syndrome
  • Aliases:
    • Choanal atresia - deafness - cardiac defects - dysmorphism syndrome
Homo sapiens (human)
DOID:0080694
  • Galloway-Mowat syndrome
Homo sapiens (human)
DOID:0080693
  • Noonan syndrome-like disorder with loose anagen hair 2
Homo sapiens (human)
DOID:0080692
  • Noonan syndrome-like disorder with loose anagen hair 1
Homo sapiens (human)
DOID:0080691
  • Noonan syndrome-like disorder with loose anagen hair
Homo sapiens (human)
DOID:0080690
  • RASopathy
  • Aliases:
    • RAS/mitogen-activated protein kinase syndrome
Homo sapiens (human)
DOID:0080689
  • mosaic variegated aneuploidy syndrome 3
Homo sapiens (human)
DOID:0080688
  • mosaic variegated aneuploidy syndrome
Homo sapiens (human)
DOID:0080687
  • reducing body myopathy 1B
Homo sapiens (human)
DOID:0080686
  • tubular aggregate myopathy 2
Homo sapiens (human)
DOID:0080685
  • aortic dissection
Homo sapiens (human)
DOID:0080684
  • diffuse midline glioma, H3 K27M-mutant
  • Aliases:
    • diffuse intrinsic pontine glioma
Homo sapiens (human)
DOID:0080681
  • X-linked chronic idiopathic intestinal pseudo-obstruction
Homo sapiens (human)
DOID:0080679
  • neuronal intestinal dysplasia type A
Homo sapiens (human)
DOID:0080678
  • mucolipidosis III gamma
Homo sapiens (human)
DOID:0080677
  • otospondylomegaepiphyseal dysplasia, autosomal dominant
Homo sapiens (human)
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Last updated: December 9, 2024