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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 7001 - 7025 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼ Source
DOID:6132
  • bronchitis
  • Aliases:
    • CI - Chest infection
    • Chest infection
    • acute Bronchitis
    • chest cold
    • chronic bronchitis
    • recurrent wheezy bronchitis
Mus musculus (house mouse)
DOID:0081399
  • autosomal dominant distal hereditary motor neuronopathy 10
Mus musculus (house mouse)
DOID:2450
  • central retinal vein occlusion
Mus musculus (house mouse)
DOID:0112136
  • severe congenital neutropenia 4
  • Aliases:
    • Dursun syndrome
    • SCN4
    • autosomal recessive severe congenital neutropenia due to G6PC3 deficiency
    • severe congenital neutropenia-pulmonary hypertension-superficial venous angiectasis syndrome
Mus musculus (house mouse)
DOID:0112230
  • lissencephaly 5
  • Aliases:
    • LIS5
Mus musculus (house mouse)
DOID:0110019
  • age related macular degeneration 7
  • Aliases:
    • ARMD7
Mus musculus (house mouse)
DOID:0060856
  • right atrial isomerism
  • Aliases:
    • Ivemark syndrome
    • asplenia with cardiovascular anomalies
Mus musculus (house mouse)
DOID:0080346
  • blepharocheilodontic syndrome 2
Mus musculus (house mouse)
DOID:0080504
  • Parkinson's disease 22
  • Aliases:
    • autosomal dominant Parkinson's disease 22
Mus musculus (house mouse)
DOID:4988
  • alcoholic pancreatitis
Mus musculus (house mouse)
DOID:0111960
  • immunodeficiency 15A
  • Aliases:
    • IMD15A
Mus musculus (house mouse)
DOID:10485
  • esophageal atresia
  • Aliases:
    • Congenital atresia of esophagus
    • Congenital imperforate esophagus
    • Imperforate esophagus
    • Oesophageal atresia
Mus musculus (house mouse)
DOID:0111558
  • Charcot-Marie-Tooth disease type 2DD
  • Aliases:
    • ATP1A1-related CMT2
    • ATP1A1-related autosomal dominant Charcot-Marie-Tooth disease type 2
    • CMT2DD
    • Charcot-Marie-Tooth disease, axonal, type 2DD
    • Charcot-Marie-Tooth neuropathy, type 2DD
Mus musculus (house mouse)
DOID:9410
  • panhypopituitarism
  • Aliases:
    • Simmond's disease
    • Simmonds' disease
    • combined pituitary hormone deficiency
Mus musculus (house mouse)
DOID:0110295
  • autosomal recessive limb-girdle muscular dystrophy type 2U
  • Aliases:
    • LGMD2U
    • MDDGC7
    • autosomal recessive limb-girdle muscular dystrophy due to ISPD deficiency
    • muscular dystrophy limb-girdle type 2U
    • muscular dystrophy-dystroglycanopathy (limb-girdle) type C7
Mus musculus (house mouse)
DOID:0112146
  • retinitis pigmentosa 89
  • Aliases:
    • RP89
Mus musculus (house mouse)
DOID:0070354
  • cataract 48
  • Aliases:
    • CTRCT48
Mus musculus (house mouse)
DOID:0080737
  • Ehlers-Danlos syndrome musculocontractural type 2
Mus musculus (house mouse)
DOID:0111467
  • combined oxidative phosphorylation deficiency 13
  • Aliases:
    • COXPD13
Mus musculus (house mouse)
DOID:0111105
  • maturity-onset diabetes of the young type 8
  • Aliases:
    • MODY type 8
    • MODY8
    • diabetes and pancreatic exocrine
    • maturity-onset diabetes of the young type 8 with exocrine dysfunction
Mus musculus (house mouse)
DOID:4441
  • dysgerminoma
Mus musculus (house mouse)
DOID:0050820
  • atrioventricular block
  • Aliases:
    • AV block
Mus musculus (house mouse)
DOID:0080899
  • lung pleomorphic carcinoma
Mus musculus (house mouse)
DOID:13372
  • alpha 1-antitrypsin deficiency
  • Aliases:
    • AAT deficiency
Mus musculus (house mouse)
DOID:0070509
  • Schinzel Giedion syndrome
  • Aliases:
    • SGS
    • Schinzel-Giedion midface retraction syndrome
Mus musculus (house mouse)
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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