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 826 - 850 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism
DOID:0050650
  • familial atrial fibrillation
  • Aliases:
    • ATFB
Homo sapiens (human)
DOID:0050793
  • short QT syndrome
Homo sapiens (human)
DOID:0110644
  • long QT syndrome 1
  • Aliases:
    • LQT1
    • ventricular fibrillation with prolonged QT interval
Homo sapiens (human)
DOID:2842
  • Jervell-Lange Nielsen syndrome
  • Aliases:
    • Jervell and Lange-Nielson syndrome
Homo sapiens (human)
DOID:0070119
  • Meckel syndrome 5
  • Aliases:
    • MKS5
    • Meckel-Gruber syndrome, type 5
Homo sapiens (human)
DOID:0070116
  • Meckel syndrome 2
  • Aliases:
    • MKS2
    • Meckel-Gruber syndrome, type 2
Homo sapiens (human)
DOID:0070118
  • Meckel syndrome 4
  • Aliases:
    • MKS4
    • Meckel-Gruber syndrome, type 4
Homo sapiens (human)
DOID:0070120
  • Meckel syndrome 6
  • Aliases:
    • MKS6
    • Meckel-Gruber syndrome, type 6
Homo sapiens (human)
DOID:0070117
  • Meckel syndrome 3
  • Aliases:
    • MKS3
    • Meckel-Gruber syndrome, type 3
Homo sapiens (human)
DOID:0111110
  • maturity-onset diabetes of the young type 13
  • Aliases:
    • MODY type 13
    • MODY13
Homo sapiens (human)
DOID:0110657
  • congenital myasthenic syndrome 8
  • Aliases:
    • CMS8
    • congenital myasthenic syndrome 8 with pre- and postsynaptic defects
    • congenital myasthenic syndrome due to agrin deficiency
Homo sapiens (human)
DOID:0110668
  • congenital myasthenic syndrome 10
  • Aliases:
    • CMS10
    • LGM
    • congenital muscular dystrophy merosin-positive
    • familial limb-girdle myasthenia
Homo sapiens (human)
DOID:0050877
  • pancreatic agenesis
  • Aliases:
    • Agenesis of the dorsal pancreas
    • partial pancreatic agenesis
Homo sapiens (human)
DOID:0111103
  • maturity-onset diabetes of the young type 4
  • Aliases:
    • MODY type 4
    • MODY4
Homo sapiens (human)
DOID:0060849
  • osteoporosis-pseudoglioma syndrome
  • Aliases:
    • OPPG
    • ocular form of osteogenesis imperfecta
Homo sapiens (human)
DOID:9857
  • interstitial keratitis
Homo sapiens (human)
DOID:0070014
  • autosomal dominant dyskeratosis congenita 1
  • Aliases:
    • DKCA1
    • Dyskeratosis Congenita, Scoggins Type
Homo sapiens (human)
DOID:0111108
  • maturity-onset diabetes of the young type 10
  • Aliases:
    • MODY10
Homo sapiens (human)
DOID:0081221
  • autosomal recessive intellectual developmental disorder 59
Homo sapiens (human)
DOID:0080596
  • hyper IgE recurrent infection syndrome 4
Homo sapiens (human)
DOID:6227
  • articular cartilage disease
Homo sapiens (human)
DOID:11121
  • pulpitis
  • Aliases:
    • pulp stones
Homo sapiens (human)
DOID:5339
  • cyclic hematopoiesis
  • Aliases:
    • Cyclic neutropenia
    • Cyclical neutropenia
    • Neutropenia, periodic
    • cyclic agranulocytosis
Homo sapiens (human)
DOID:0060280
  • primary pigmented nodular adrenocortical disease
Homo sapiens (human)
DOID:0050437
  • Danon disease
  • Aliases:
    • ANTOPOL DISEASE
    • PSEUDOGLYCOGENOSIS II
Homo sapiens (human)

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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: August 19, 2024