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 976 - 1000 of 4621 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism
DOID:0080572
  • congenital disorder of glycosylation Iw
  • Aliases:
    • congenital disorder of glycosylation 1w
Homo sapiens (human)
DOID:0080573
  • congenital disorder of glycosylation Ix
  • Aliases:
    • congenital disorder of glycosylation 1x
Homo sapiens (human)
DOID:0080575
  • Larsen-like syndrome B3GAT3 type
  • Aliases:
    • Larsen-like syndrome, B3GAT3 type
    • multiple joint dislocations-short stature-craniofacial dysmorphism-congenital heart defects syndrome
Homo sapiens (human)
DOID:0080576
  • spondyloepimetaphyseal dysplasia, Genevieve-type
Homo sapiens (human)
DOID:0080582
  • hypotrichosis 14
Homo sapiens (human)
DOID:0080587
  • congenital myasthenic syndrome 22
Homo sapiens (human)
DOID:0080596
  • hyper IgE recurrent infection syndrome 4
Homo sapiens (human)
DOID:0080599
  • Coronavirus infectious disease
Homo sapiens (human)
DOID:0080600
  • COVID-19
  • Aliases:
    • 2019 Novel Coronavirus (2019-nCoV)
    • 2019-nCoV infection
    • COVID19
    • SARS-CoV-2 infection
    • Wuhan coronavirus infection
    • Wuhan seafood market pneumonia virus infection
Homo sapiens (human)
DOID:0080611
  • anterior segment dysgenesis 6
Homo sapiens (human)
DOID:0080626
  • corticosterone methyloxidase deficiency 1
  • Aliases:
    • aldosterone synthase deficiency
Homo sapiens (human)
DOID:0080630
  • B-lymphoblastic leukemia/lymphoma
  • Aliases:
    • B lymphoblastic leukemia/lymphoma
    • B-ALL
    • precursor B lymphoblastic lymphoma/leukemia
Homo sapiens (human)
DOID:0080633
  • developmental cardiac valvular defect
Homo sapiens (human)
DOID:0080664
  • diaphyseal medullary stenosis with malignant fibrous histiocytoma
  • Aliases:
    • Hardcastle syndrome
    • bone dysplasia-medullary fibrosarcoma syndrome
    • diaphyseal medullary stenosis-malignant fibrous histiocytoma syndrome
Homo sapiens (human)
DOID:0080665
  • warfarin resistance
Homo sapiens (human)
DOID:0080678
  • mucolipidosis III gamma
Homo sapiens (human)
DOID:0080693
  • Noonan syndrome-like disorder with loose anagen hair 2
Homo sapiens (human)
DOID:0080718
  • GNE myopathy
  • Aliases:
    • Distal myopathy, Nonaka type
    • Hereditary Inclusion Body Myopathy
    • Nonaka myopathy
    • inclusion body myopathy 2
Homo sapiens (human)
DOID:0080721
  • calvarial doughnut lesions with bone fragility
Homo sapiens (human)
DOID:0080736
  • Ehlers-Danlos syndrome musculocontractural type 1
Homo sapiens (human)
DOID:0080737
  • Ehlers-Danlos syndrome musculocontractural type 2
Homo sapiens (human)
DOID:0080738
  • Ehlers-Danlos syndrome spondylodysplastic type 1
Homo sapiens (human)
DOID:0080750
  • erythema nodosum
Homo sapiens (human)
DOID:0080753
  • keratosis follicularis spinulosa decalvans
Homo sapiens (human)
DOID:0080759
  • Fanconi renotubular syndrome 3
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: August 19, 2024