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 1851 - 1875 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism
DOID:3490
  • Noonan syndrome
  • Aliases:
    • Turner's phenotype, karyotype normal
Homo sapiens (human)
DOID:0060588
  • Noonan syndrome 10
  • Aliases:
    • NS10
Homo sapiens (human)
DOID:0060608
  • microcephalic osteodysplastic primordial dwarfism type I
  • Aliases:
    • Taybi-Linder syndrome
    • brachymelic primordial dwarfism
    • cephaloskeletal dysplasia
    • low-birth-weight dwarfism with skeletal dysplasia
    • osteodysplastic primordial dwarfism type I
Homo sapiens (human)
DOID:0060766
  • autosomal dominant Robinow syndrome 1
  • Aliases:
    • DRS1
Homo sapiens (human)
DOID:6420
  • pulmonary valve stenosis
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:0070256
  • congenital disorder of glycosylation type IId
  • Aliases:
    • CDG IId
    • CDG2D
    • CDGIId
Homo sapiens (human)
DOID:0080738
  • Ehlers-Danlos syndrome spondylodysplastic type 1
Homo sapiens (human)
DOID:9669
  • senile cataract
Homo sapiens (human)
DOID:3827
  • congenital diaphragmatic hernia
  • Aliases:
    • Diaphragmatic Hernia
Homo sapiens (human)
DOID:12642
  • hiatus hernia
  • Aliases:
    • Diaphragmatic - hiatus -hernia
    • hiatal hernia
Homo sapiens (human)
DOID:1673
  • pneumothorax
Homo sapiens (human)
DOID:14775
  • brittle cornea syndrome 1
  • Aliases:
    • type VIB Ehlers-Danlos syndrome
Homo sapiens (human)
DOID:0080736
  • Ehlers-Danlos syndrome musculocontractural type 1
Homo sapiens (human)
DOID:3590
  • gestational trophoblastic neoplasm
  • Aliases:
    • gestational trophoblastic neoplasia
    • hydatidiform mole
    • molar pregnancy
Homo sapiens (human)
DOID:9955
  • hypoplastic left heart syndrome
Homo sapiens (human)
DOID:5426
  • primary ovarian insufficiency
  • Aliases:
    • hypergonadotropic hypogonadism
    • premature ovarian failure
    • premature ovarian insufficiency
Homo sapiens (human)
DOID:8670
  • eating disorder
Homo sapiens (human)
DOID:0090004
  • progressive pseudorheumatoid arthropathy of childhood
  • Aliases:
    • spondyloepiphyseal dysplasia tarda-progressive arthropathy syndrome
Homo sapiens (human)
DOID:14693
  • Clouston syndrome
  • Aliases:
    • Clouston's hidrotic ectodermal dysplasia
    • Clouston's syndrome
    • Hidrotic ectodermal dysplasia syndrome
    • ectodermal dysplasia 2, Clouston type
    • hidrotic ectodermal dysplasia
Homo sapiens (human)
DOID:5223
  • infertility
Homo sapiens (human)
DOID:12978
  • Plasmodium vivax malaria
  • Aliases:
    • Malaria by Plasmodium vivax
    • Vivax Malaria
Homo sapiens (human)
DOID:724
  • female stress incontinence
  • Aliases:
    • Stress incontinence - female
    • female urinary stress incontinence
Homo sapiens (human)
DOID:2320
  • obstructive lung disease
  • Aliases:
    • respiratory airway obstruction
Homo sapiens (human)
DOID:0080482
  • peroxisome biogenesis disorder 7A
  • Aliases:
    • peroxisome biogenesis disorder 7A (Zellweger)
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