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 2601 - 2625 of 4621 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism
DOID:7465
  • chronic NK-cell lymphocytosis
  • Aliases:
    • NK-cell large granular Lymphocyte Lymphocytosis
Homo sapiens (human)
DOID:9155
  • mucocutaneous leishmaniasis
  • Aliases:
    • American cutaneous leishmaniasis
    • American mucocutaneous leishmaniasis
    • Cutaneous leishmaniasis, American
    • Mucocutaneous leishmaniasis, American
    • New World cutaneous leishmaniasis
Homo sapiens (human)
DOID:2047
  • hepatitis D
  • Aliases:
    • delta hepatitis
Homo sapiens (human)
DOID:4617
  • periapical granuloma
  • Aliases:
    • Apical granuloma
Homo sapiens (human)
DOID:3223
  • complex regional pain syndrome
  • Aliases:
    • Complex regional pain syndromes
Homo sapiens (human)
DOID:4308
  • polyradiculoneuropathy
Homo sapiens (human)
DOID:7319
  • axonal neuropathy
Homo sapiens (human)
DOID:6404
  • metanephric adenoma
Homo sapiens (human)
DOID:11042
  • Felty's syndrome
  • Aliases:
    • Felty syndrome
    • Rheumatoid arthritis with splenoadenomegaly and leukopenia
Homo sapiens (human)
DOID:0080575
  • Larsen-like syndrome B3GAT3 type
  • Aliases:
    • Larsen-like syndrome, B3GAT3 type
    • multiple joint dislocations-short stature-craniofacial dysmorphism-congenital heart defects syndrome
Homo sapiens (human)
DOID:10376
  • amblyopia
  • Aliases:
    • lazy eye
Homo sapiens (human)
DOID:10375
  • strabismic amblyopia
  • Aliases:
    • suppression amblyopia
Homo sapiens (human)
DOID:14004
  • thoracic aortic aneurysm
Homo sapiens (human)
DOID:9835
  • refractive error
Homo sapiens (human)
DOID:0080520
  • Tn polyagglutination syndrome
  • Aliases:
    • galactosyltransferase deficiency
Homo sapiens (human)
DOID:9296
  • cleft lip
  • Aliases:
    • Labium leporinum
    • cheiloschisis
    • cleft lip, unilateral, complete
    • complete unilateral cleft lip
    • hare lip
Homo sapiens (human)
DOID:0080073
  • spina bifida occulta
Homo sapiens (human)
DOID:10488
  • imperforate anus
  • Aliases:
    • Congenital atresia of anus
    • Congenital or infantile occlusion of anus
    • anal atresia
Homo sapiens (human)
DOID:0080204
  • renal hypoplasia
Homo sapiens (human)
DOID:14686
  • Axenfeld-Rieger syndrome
  • Aliases:
    • Anomaly, Rieger's
    • Axenfeld syndrome
    • RGS - Rieger syndrome
    • Rieger's anomaly
Homo sapiens (human)
DOID:0060055
  • popliteal pterygium syndrome
  • Aliases:
    • facio-genito-popliteal syndrome
    • popliteal web syndrome
Homo sapiens (human)
DOID:0060246
  • MASA syndrome
  • Aliases:
    • CRASH syndrome
    • Gareis-Mason syndrome
    • L1 syndrome
    • SPG1
    • X-linked complicated hereditary spastic paraplegia type 1
    • X-linked corpus callosum agenesis
    • X-linked spastic paraplegia 1
    • hereditary spastic paraplegia 1
Homo sapiens (human)
DOID:5003
  • eunuchism
Homo sapiens (human)
DOID:4610
  • intestinal benign neoplasm
  • Aliases:
    • intestinal tumors
    • intestine growth
    • neoplasm of intestinal tract
Homo sapiens (human)
DOID:10155
  • intestinal cancer
  • Aliases:
    • malignant intestinal tumors
    • malignant neoplasm of intestine
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: August 19, 2024