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 3326 - 3350 of 4649 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism Source
DOID:12558
  • chronic progressive external ophthalmoplegia
  • Aliases:
    • progressive external ophthalmoplegia
Homo sapiens (human)
DOID:12559
  • idiopathic juvenile osteoporosis
  • Aliases:
    • Idiopathic osteoporosis
    • juvenile osteoporosis
Homo sapiens (human)
DOID:12574
  • posterior uveitis
  • Aliases:
    • Uveitis, posterior
Homo sapiens (human)
DOID:12577
  • urethral obstruction
  • Aliases:
    • Obstruction of urethra
Homo sapiens (human)
DOID:12583
  • velocardiofacial syndrome
  • Aliases:
    • Shprintzen syndrome
    • VCF-Velocardiofacial syndrome
Homo sapiens (human)
DOID:12638
  • hypertrophic pyloric stenosis
  • Aliases:
    • congenital hypertrophic pyloric stenosis
    • congenital or infantile stricture of pylorus
Homo sapiens (human)
DOID:12662
  • paracoccidioidomycosis
  • Aliases:
    • Mucocutaneous-lymphangitic paracoccidioidomycosis
    • paracoccidioidal mycosis
Homo sapiens (human)
DOID:12678
  • hypercalcemia
Homo sapiens (human)
DOID:12679
  • nephrocalcinosis
Homo sapiens (human)
DOID:12689
  • acoustic neuroma
  • Aliases:
    • Vestibular Neurilemmoma
    • Vestibular schwannoma
Homo sapiens (human)
DOID:127
  • leiomyoma
  • Aliases:
    • leiomyomatous neoplasm
    • leiomyomatous tumor
Homo sapiens (human)
DOID:1270
  • hereditary hemorrhagic telangiectasia
  • Aliases:
    • Osler hemorrhagic telangiectasia syndrome
    • Osler-Weber-Rendu disease
    • Rendu-Osler-Weber disease
Homo sapiens (human)
DOID:12700
  • hyperprolactinemia
  • Aliases:
    • Chiari-Frommel syndrome
    • Pregnancy-related A-G syndrome
    • hyperprolactinaemia
Homo sapiens (human)
DOID:12704
  • ataxia telangiectasia
  • Aliases:
    • Boder-Sedgwick syndrome
    • Louis Bar syndrome
Homo sapiens (human)
DOID:12705
  • Friedreich ataxia
  • Aliases:
    • Friedreich's ataxia
    • Friedreich's tabes
Homo sapiens (human)
DOID:12712
  • nephronophthisis
  • Aliases:
    • medullary cystic disease
    • medullary cystic kidney
Homo sapiens (human)
DOID:12714
  • Ellis-Van Creveld syndrome
  • Aliases:
    • Chondroectodermal dysplasia
    • mesoectodermal dysplasia
Homo sapiens (human)
DOID:12716
  • newborn respiratory distress syndrome
  • Aliases:
    • HMD - Hyaline membrane disease
    • Neonatal respiratory Distress syndrome
    • hyaline membrane disease
    • pulmonary hyaline membrane disease
    • pulmonary hypoperfusion syndrome of newborn
    • respiratory distress syndrome of newborn
Homo sapiens (human)
DOID:1272
  • telangiectasis
  • Aliases:
    • telangiectasia
Homo sapiens (human)
DOID:12720
  • cerebral atherosclerosis
Homo sapiens (human)
DOID:12721
  • multiple epiphyseal dysplasia
  • Aliases:
    • polyepiphyseal dysplasia
Homo sapiens (human)
DOID:1273
  • respiratory syncytial virus infectious disease
  • Aliases:
    • RSV
    • respiratory syncytial virus
Homo sapiens (human)
DOID:12732
  • intermediate uveitis
  • Aliases:
    • chronic cyclitis
    • peripheral uveoretinitis
Homo sapiens (human)
DOID:12783
  • migraine without aura
  • Aliases:
    • common migraine
Homo sapiens (human)
DOID:12798
  • mucopolysaccharidosis
Homo sapiens (human)

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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