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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 14751 - 14775 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism Source
DOID:824
  • periodontitis
  • Aliases:
    • chronic pericementitis
Xenopus laevis (African clawed frog)
DOID:11664
  • nephrosclerosis
  • Aliases:
    • renal sclerosis
Xenopus laevis (African clawed frog)
DOID:13544
  • low tension glaucoma
  • Aliases:
    • Normal tension glaucoma
Xenopus laevis (African clawed frog)
DOID:1712
  • aortic valve stenosis
  • Aliases:
    • Aortic stenosis
    • Rheumatic aortic stenosis
    • rheumatic aortic valve stenosis
Xenopus laevis (African clawed frog)
DOID:1485
  • cystic fibrosis
  • Aliases:
    • CF
    • mucoviscidosis
Xenopus laevis (African clawed frog)
DOID:3083
  • chronic obstructive pulmonary disease
  • Aliases:
    • COLD
    • COPD
    • chronic obstructive airway disease
    • chronic obstructive lung disease
Xenopus laevis (African clawed frog)
DOID:0050848
  • obstructive sleep apnea
  • Aliases:
    • obstructive sleep apnea syndrome
Xenopus laevis (African clawed frog)
DOID:1287
  • cardiovascular system disease
  • Aliases:
    • disease of subdivision of hemolymphoid system
Xenopus laevis (African clawed frog)
DOID:0050731
  • vitamin B12 deficiency
  • Aliases:
    • cobalamin deficiency
    • hypocobalaminemia
Xenopus laevis (African clawed frog)
DOID:0112198
  • spondyloepimetaphyseal dysplasia with joint laxity type 1
  • Aliases:
    • SEMDJL1
    • spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures
Xenopus laevis (African clawed frog)
DOID:0050802
  • Ehlers-Danlos syndrome spondylodysplastic type 2
  • Aliases:
    • EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 2
    • Ehlers-Danlos syndrome progeroid type
Xenopus laevis (African clawed frog)
DOID:0080564
  • congenital disorder of glycosylation Il
  • Aliases:
    • congenital disorder of glycosylation 1l
Xenopus laevis (African clawed frog)
DOID:0110676
  • congenital myasthenic syndrome 13
  • Aliases:
    • CMS13
    • CMSTA2
    • congenital myasthenic syndrome 13 with tubular aggregates
    • congenital myasthenic syndrome with tubular aggregates 2
Xenopus laevis (African clawed frog)
DOID:0080562
  • congenital disorder of glycosylation Ij
  • Aliases:
    • Congenital disorder of glycosylation 1j
Xenopus laevis (African clawed frog)
DOID:0050813
  • spondyloepiphyseal dysplasia with congenital joint dislocations
  • Aliases:
    • CHONDRODYSPLASIA WITH MULTIPLE DISLOCATIONS
    • CHST3-Related Skeletal Dysplasia
    • Humero-spinal dysostosis with congenital heart disease
    • Kozlowski Celermajer Tink syndrome
    • Omani Type
    • Spondyloepiphyseal Dysplasia
    • humero-spinal dysostosis
    • humerospinal dysostosis
Xenopus laevis (African clawed frog)
DOID:2256
  • osteochondrodysplasia
  • Aliases:
    • Cartilage Development disorder
    • Congenital anomaly of cartilage
    • Osteochondrodysplasia syndrome
    • chondrodystrophy
    • skeletal dysplasia
Xenopus laevis (African clawed frog)
DOID:14766
  • renal agenesis
  • Aliases:
    • hereditary renal aplasia
    • hereditary urogenital adysplasia
    • renal adysplasia
    • renal aplasia
Xenopus laevis (African clawed frog)
DOID:9810
  • polyarteritis nodosa
Xenopus laevis (African clawed frog)
DOID:3049
  • Churg-Strauss syndrome
  • Aliases:
    • Allergic Granulomatous Angiitis
    • Allergic granulomatosis angiitis
    • Churg-Strauss vasculitis
Xenopus laevis (African clawed frog)
DOID:2377
  • multiple sclerosis
  • Aliases:
    • Generalized multiple sclerosis
    • insular sclerosis
Xenopus laevis (African clawed frog)
DOID:0111331
  • intellectual disability-severe speech delay-mild dysmorphism syndrome
  • Aliases:
    • FOXP1 Haploinsufficiency
    • FOXP1 syndrome
    • FOXP1-Related Neurodevelopmental Disorder
    • Mental retardation with language impairment and with or without autistic features
Mus musculus (house mouse)
DOID:1255
  • trichostrongyloidiasis
Mus musculus (house mouse)
DOID:0060038
  • specific developmental disorder
Mus musculus (house mouse)
DOID:9955
  • hypoplastic left heart syndrome
Mus musculus (house mouse)
DOID:0090131
  • complex cortical dysplasia with other brain malformations
  • Aliases:
    • CDCBM
Mus musculus (house mouse)
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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