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 1376 - 1400 of 4649 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism Source
DOID:0080634
  • nanophthalmos
Homo sapiens (human)
DOID:0080641
  • tongue carcinoma
Homo sapiens (human)
DOID:0080642
  • Middle East respiratory syndrome
Homo sapiens (human)
DOID:0080652
  • calcium oxalate nephrolithiasis
Homo sapiens (human)
DOID:0080653
  • urolithiasis
Homo sapiens (human)
DOID:0080661
  • nonsyndromic aplasia cutis congenita
Homo sapiens (human)
DOID:0080663
  • atrial standstill 2
Homo sapiens (human)
DOID:0080664
  • diaphyseal medullary stenosis with malignant fibrous histiocytoma
  • Aliases:
    • Hardcastle syndrome
    • bone dysplasia-medullary fibrosarcoma syndrome
    • diaphyseal medullary stenosis-malignant fibrous histiocytoma syndrome
Homo sapiens (human)
DOID:0080665
  • warfarin resistance
Homo sapiens (human)
DOID:0080669
  • posterior polymorphous corneal dystrophy 4
Homo sapiens (human)
DOID:0080672
  • fibrochondrogenesis 1
Homo sapiens (human)
DOID:0080673
  • fibrochondrogenesis 2
Homo sapiens (human)
DOID:0080675
  • Stickler syndrome 2
Homo sapiens (human)
DOID:0080676
  • Stickler syndrome 1
Homo sapiens (human)
DOID:0080677
  • otospondylomegaepiphyseal dysplasia, autosomal dominant
Homo sapiens (human)
DOID:0080678
  • mucolipidosis III gamma
Homo sapiens (human)
DOID:0080679
  • neuronal intestinal dysplasia type A
Homo sapiens (human)
DOID:0080681
  • X-linked chronic idiopathic intestinal pseudo-obstruction
Homo sapiens (human)
DOID:0080684
  • diffuse midline glioma, H3 K27M-mutant
  • Aliases:
    • diffuse intrinsic pontine glioma
Homo sapiens (human)
DOID:0080685
  • aortic dissection
Homo sapiens (human)
DOID:0080686
  • tubular aggregate myopathy 2
Homo sapiens (human)
DOID:0080687
  • reducing body myopathy 1B
Homo sapiens (human)
DOID:0080688
  • mosaic variegated aneuploidy syndrome
Homo sapiens (human)
DOID:0080689
  • mosaic variegated aneuploidy syndrome 3
Homo sapiens (human)
DOID:0080690
  • RASopathy
  • Aliases:
    • RAS/mitogen-activated protein kinase syndrome
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