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 2626 - 2650 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism
DOID:0060256
  • Dowling-Degos disease
  • Aliases:
    • dark dot disease
    • reticular pigment anomaly of flexures
Homo sapiens (human)
DOID:0050663
  • Bethlem myopathy
  • Aliases:
    • benign congenital muscular dystrophy
Homo sapiens (human)
DOID:0050558
  • Ullrich congenital muscular dystrophy
  • Aliases:
    • ULLRICH DISEASE
    • Ullrich scleroatonic muscular dystrophy
Homo sapiens (human)
DOID:10041
  • dysplastic nevus syndrome
  • Aliases:
    • FAMM syndrome
    • familial atypical multiple mole-melanoma
Homo sapiens (human)
DOID:0080952
  • AMED syndrome
  • Aliases:
    • AMEDS
Homo sapiens (human)
DOID:2855
  • hyperthyroxinemia
Homo sapiens (human)
DOID:9279
  • hyperhomocysteinemia
Homo sapiens (human)
DOID:13636
  • Fanconi anemia
  • Aliases:
    • Fanconi anaemia
    • Fanconi pancytopenia
    • Fanconi panmyelopathy
    • Fanconi's anaemia
    • Fanconi's anemia
Homo sapiens (human)
DOID:12450
  • pancytopenia
Homo sapiens (human)
DOID:0080101
  • Compton-North congenital myopathy
  • Aliases:
    • congenital myopathy 12
Homo sapiens (human)
DOID:5213
  • chronic inflammatory demyelinating polyradiculoneuropathy
Homo sapiens (human)
DOID:2536
  • chronic inflammatory demyelinating polyneuritis
Homo sapiens (human)
DOID:0111377
  • fetal akinesia deformation sequence syndrome 1
  • Aliases:
    • FADS1
Homo sapiens (human)
DOID:0111375
  • fetal akinesia deformation sequence syndrome
  • Aliases:
    • FADS
    • Pena-Shokeir syndrome type 1
    • arthrogryposis multiplex congenita-pulmonary hypoplasia syndrome
    • fetal akinesia sequence
    • foetal akinesia deformation sequence syndrome
    • foetal akinesia sequence
Homo sapiens (human)
DOID:12889
  • Miller Fisher syndrome
  • Aliases:
    • Fisher's syndrome
    • Miller-Fisher variant of Guillain-Barre syndrome
Homo sapiens (human)
DOID:12842
  • Guillain-Barre syndrome
  • Aliases:
    • Infectious neuronitis
    • Post-infectious polyneuritis
    • Postinfectious polyneuritis
    • acute infective polyneuritis
    • acute inflammatory demyelinating polyradiculopathy
    • acute postinfectious polyneuropathy
Homo sapiens (human)
DOID:12377
  • spinal muscular atrophy
Homo sapiens (human)
DOID:0060294
  • cold-induced sweating syndrome
  • Aliases:
    • Crisponi syndrome
    • Sohar-Crisponi syndrome
Homo sapiens (human)
DOID:0080329
  • cold-induced sweating syndrome 1
Homo sapiens (human)
DOID:0112198
  • spondyloepimetaphyseal dysplasia with joint laxity type 1
  • Aliases:
    • SEMDJL1
    • spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures
Homo sapiens (human)
DOID:0111148
  • isolated ectopia lentis
  • Aliases:
    • IEL
    • familial ectopia lentis
Homo sapiens (human)
DOID:319
  • spinal cord disease
Homo sapiens (human)
DOID:0080332
  • bicuspid aortic valve disease
  • Aliases:
    • Familial bicuspid aortic valve
Homo sapiens (human)
DOID:0080333
  • aortic valve disease 1
Homo sapiens (human)
DOID:11502
  • mitral valve insufficiency
  • Aliases:
    • Congenital insufficiency of mitral valve
    • Mitral valve incompetence
    • congenital mitral insufficiency
    • congenital mitral regurgitation
    • mitral regurgitation
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: August 19, 2024