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 July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 5801 - 5825 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼
DOID:0112319
  • Kanzaki disease
  • Aliases:
    • NAGA deficiency type 2
    • adult-onset alpha-N-acetylgalactosaminidase deficiency
    • alpha-N-acetylgalactosaminidase deficiency type 2
Homo sapiens (human)
DOID:8986
  • narcolepsy
  • Aliases:
    • Narcolepsy, without cataplexy
    • paroxysmal sleep
Homo sapiens (human)
DOID:0110594
  • primary ciliary dyskinesia 1
  • Aliases:
    • CILD1
    • primary ciliary dyskinesia 1 with or without situs inversus
Homo sapiens (human)
DOID:9256
  • colorectal cancer
Homo sapiens (human)
DOID:3947
  • adrenal gland hyperfunction
  • Aliases:
    • Adrenocortical hyperfunction
    • hyperadrenalism
    • hypercortisolism
Homo sapiens (human)
DOID:12574
  • posterior uveitis
  • Aliases:
    • Uveitis, posterior
Homo sapiens (human)
DOID:11914
  • gastroparesis
  • Aliases:
    • Gastroparalysis
    • Gastroparesis syndrome
    • gastric atonia
Homo sapiens (human)
DOID:0110264
  • cataract 33
  • Aliases:
    • CTRCT33
Homo sapiens (human)
DOID:2537
  • inflammatory and toxic neuropathy
Homo sapiens (human)
DOID:0111460
  • cardiofaciocutaneous syndrome 1
  • Aliases:
    • CFC1
Homo sapiens (human)
DOID:4239
  • alveolar soft part sarcoma
Homo sapiens (human)
DOID:2938
  • Epstein-Barr virus infectious disease
  • Aliases:
    • EBV Infection
    • Epstein-Barr virus infection
Homo sapiens (human)
DOID:718
  • autoimmune hemolytic anemia
  • Aliases:
    • Autoimmune haemolytic anaemia
    • autoimmune hemolytic anaemia
Homo sapiens (human)
DOID:0110546
  • autosomal dominant nonsyndromic deafness 15
  • Aliases:
    • DFNA15
    • autosomal dominant deafness 15
Homo sapiens (human)
DOID:0110826
  • Usher syndrome type 1
  • Aliases:
    • US1
    • USH1
Homo sapiens (human)
DOID:0080195
  • Marinesco-Sjogren syndrome
  • Aliases:
    • Garland-Moorhouse syndrome
    • Marinesco-Garland syndrome
    • Oligophrenic cerebellolenticular degeneration
    • hereditary oligophrenic cerebello-lental degeneration
Homo sapiens (human)
DOID:13628
  • favism
Homo sapiens (human)
DOID:0050741
  • alcohol dependence
  • Aliases:
    • alcoholism
Homo sapiens (human)
DOID:1591
  • renovascular hypertension
Homo sapiens (human)
DOID:0111441
  • optic atrophy 1
  • Aliases:
    • OPA1
Homo sapiens (human)
DOID:13197
  • nodular goiter
  • Aliases:
    • Goiter, nodular
    • nodular goitre
Homo sapiens (human)
DOID:4810
  • cerebrotendinous xanthomatosis
  • Aliases:
    • Cholestanol storage disease
Homo sapiens (human)
DOID:2474
  • vernal conjunctivitis
Homo sapiens (human)
DOID:0110340
  • osteogenesis imperfecta type 4
  • Aliases:
    • OI4
    • osteogenesis imperfecta type IV
    • osteogenesis imperfecta with normal sclera
Homo sapiens (human)
DOID:1270
  • hereditary hemorrhagic telangiectasia
  • Aliases:
    • Osler hemorrhagic telangiectasia syndrome
    • Osler-Weber-Rendu disease
    • Rendu-Osler-Weber disease
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