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 8876 - 8900 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼ Source
DOID:11263
  • chlamydia
  • Aliases:
    • Chlamydia trachomatis infectious disease
    • Chlamydial Infection
    • chlamydial disease
Homo sapiens (human)
DOID:0111892
  • Diamond-Blackfan anemia 11
  • Aliases:
    • DBA11
    • RPL26-related Diamond-Blackfan anemia
Homo sapiens (human)
DOID:12528
  • lesion of sciatic nerve
Homo sapiens (human)
DOID:0050876
  • Caroli disease
Homo sapiens (human)
DOID:0090143
  • brachyolmia-amelogenesis imperfecta syndrome
  • Aliases:
    • DASS
    • STHAG6
    • dental anomalies and short stature
    • platyspondyly with amelogenesis imperfecta
    • selective tooth agenesis 5
Homo sapiens (human)
DOID:11717
  • neonatal diabetes
  • Aliases:
    • diabetes mellitus syndrome in newborn infant
    • neonatal diabetes mellitus
Homo sapiens (human)
DOID:9256
  • colorectal cancer
Homo sapiens (human)
DOID:0111495
  • combined oxidative phosphorylation deficiency 33
  • Aliases:
    • COXPD33
Homo sapiens (human)
DOID:3227
  • tracheal stenosis
  • Aliases:
    • Stenosis of trachea
Homo sapiens (human)
DOID:0111473
  • combined oxidative phosphorylation deficiency 5
  • Aliases:
    • COXPD5
    • hypotonia with lactic acidemia and hyperammonemia
Homo sapiens (human)
DOID:0110107
  • atrial heart septal defect 2
  • Aliases:
    • ASD2
    • atrial septal defect 2
Homo sapiens (human)
DOID:0081143
  • agammaglobulinemia 8B
Homo sapiens (human)
DOID:0080758
  • Fanconi renotubular syndrome 2
Homo sapiens (human)
DOID:0111401
  • congenital dyserythropoietic anemia type II
  • Aliases:
    • CDA II
    • CDA type 2
    • CDA type II
    • CDAN2
    • Congenital dyserythropoietic anaemia type 2
    • Congenital dyserythropoietic anemia type 2
    • Hereditary erythroblastic multinuclearity with a positive acidified-serum test (hempas)
    • SEC23B-CDG
    • congenital dyserythropoietic anaemia type II
Homo sapiens (human)
DOID:13909
  • red-green color blindness
  • Aliases:
    • Deutan defect
    • Deuteranopia
    • Reduced red-green discrimination
Homo sapiens (human)
DOID:9938
  • dacryocystitis
Homo sapiens (human)
DOID:5353
  • colonic disease
  • Aliases:
    • colon disorder
Homo sapiens (human)
DOID:0080447
  • developmental and epileptic encephalopathy 43
  • Aliases:
    • DEE43
    • early infantile epileptic encephalopathy 43
Homo sapiens (human)
DOID:0060780
  • congenital diarrhea 6
  • Aliases:
    • chronic diarrhea due to guanylate cyclase 2C overactivity
    • chronic diarrhoea due to guanylate cyclase 2C overactivity
    • congenital diarrhoea 6
Homo sapiens (human)
DOID:0111598
  • distal arthrogryposis type 1B
  • Aliases:
    • DA1B
Homo sapiens (human)
DOID:13189
  • gout
  • Aliases:
    • Articular gout
    • Gouty arthropathy
    • gouty arthritis
Homo sapiens (human)
DOID:0070340
  • classic citrullinemia
Homo sapiens (human)
DOID:8506
  • bullous pemphigoid
Homo sapiens (human)
DOID:0080652
  • calcium oxalate nephrolithiasis
Homo sapiens (human)
DOID:401
  • multidrug-resistant tuberculosis
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: December 9, 2024