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 7276 - 7300 of 7942 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism
DOID:0060584
  • Noonan syndrome 6
  • Aliases:
    • NS6
Homo sapiens (human)
DOID:0060581
  • Noonan syndrome 3
  • Aliases:
    • NS3
Homo sapiens (human)
DOID:0060764
  • autosomal recessive Robinow syndrome
  • Aliases:
    • COVESDEM syndrome
    • RRS
    • costovertebral segmentation defect-mesomelia syndrome
Homo sapiens (human)
DOID:0060580
  • Noonan syndrome 2
  • Aliases:
    • NS2
Homo sapiens (human)
DOID:0060583
  • Noonan syndrome 5
  • Aliases:
    • NS5
Homo sapiens (human)
DOID:0050569
  • Seckel syndrome
  • Aliases:
    • Harper's syndrome
    • Virchow-Seckel dwarfism
    • bird-headed dwarfism
    • microcephalic primordial dwarfism
Homo sapiens (human)
DOID:0060609
  • microcephalic osteodysplastic primordial dwarfism type II
  • Aliases:
    • Majewski osteodysplastic primordial dwarfism type II
    • osteodysplastic primordial dwarfism type II
Homo sapiens (human)
DOID:6683
  • X-linked Aarskog syndrome
  • Aliases:
    • Aarskog-Scott syndrome
    • Greig's syndrome
Homo sapiens (human)
DOID:0060644
  • chondrodysplasia-pseudohermaphroditism syndrome
  • Aliases:
    • Nivelon-Nivelon-Mabille syndrome
    • chondrodysplasia-disorder of sex development syndrome
Homo sapiens (human)
DOID:0060582
  • Noonan syndrome 4
  • Aliases:
    • NS4
Homo sapiens (human)
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:14681
  • Silver-Russell syndrome
  • Aliases:
    • Silver Russell Dwarfism
Homo sapiens (human)
DOID:11983
  • Prader-Willi syndrome
  • Aliases:
    • Prader Willi syndrome
Homo sapiens (human)
DOID:11725
  • Cornelia de Lange syndrome
  • Aliases:
    • Brachmann de Lange syndrome
    • De Lange syndrome
Homo sapiens (human)
DOID:0060585
  • Noonan syndrome 7
  • Aliases:
    • NS7
Homo sapiens (human)
DOID:2962
  • Cockayne syndrome
  • Aliases:
    • Neill-Dingwall syndrome
Homo sapiens (human)
DOID:0050185
  • erythema multiforme
Homo sapiens (human)
DOID:0050426
  • Stevens-Johnson syndrome
Homo sapiens (human)
DOID:12506
  • Bell's palsy
  • Aliases:
    • Bell palsy
    • Bell's (facial) palsy
Homo sapiens (human)
DOID:1756
  • facial nerve disease
Homo sapiens (human)
DOID:13934
  • facial paralysis
  • Aliases:
    • Facial Palsy
Homo sapiens (human)
DOID:0060578
  • Noonan syndrome 1
  • Aliases:
    • NS1
Homo sapiens (human)

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024