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 726 - 750 of 4621 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism
DOID:11262
  • ornithosis
  • Aliases:
    • psittacosis
Homo sapiens (human)
DOID:11265
  • trachoma
  • Aliases:
    • active stage trachoma
    • trachoma dubium
Homo sapiens (human)
DOID:0050854
  • Muckle-Wells syndrome
  • Aliases:
    • MWS
    • neutrophilic urticaria
Homo sapiens (human)
DOID:11121
  • pulpitis
  • Aliases:
    • pulp stones
Homo sapiens (human)
DOID:0050879
  • fragile X-associated tremor/ataxia syndrome
  • Aliases:
    • FXTAS syndrome
Homo sapiens (human)
DOID:0081312
  • T-cell non-Hodgkin lymphoma
Homo sapiens (human)
DOID:1060
  • Hartnup disease
  • Aliases:
    • Neutral 1 amino acid transport defect
    • deficiency of tryptophan oxygenase
    • neutral amino acid transport defect
Homo sapiens (human)
DOID:4723
  • intracranial hypotension
Homo sapiens (human)
DOID:0111389
  • mucopolysaccharidosis Ih/s
  • Aliases:
    • MPS1H/S
    • MPSIH/S
    • Mucopolysaccharidosis type 1H/S
Homo sapiens (human)
DOID:0050466
  • Loeys-Dietz syndrome
Homo sapiens (human)
DOID:0060834
  • Griscelli syndrome type 3
  • Aliases:
    • GS3
    • Griscelli-Prunieras syndrome type 3
Homo sapiens (human)
DOID:0060832
  • Griscelli syndrome type 1
  • Aliases:
    • GS1
    • Griscelli syndrome with neurological impairment
    • Griscelli syndrome, cutaneous and neurological type
    • Griscelli-Prunieras syndrome type 1
    • hypopigmentation-neurologic impairment syndrome
Homo sapiens (human)
DOID:0110949
  • Waardenburg syndrome type 3
  • Aliases:
    • Klein-Waardenburg syndrome
    • WS3
    • Waardenburg syndrome type III
    • Waardenburg syndrome with upper limb anomalies
Homo sapiens (human)
DOID:0090100
  • ocular albinism with sensorineural deafness
  • Aliases:
    • WS2-OA
    • autosomal recessive Waardenburg syndrome type 2 with ocular albinism
    • digenic Waardenburg syndrome/albinism
    • digenic Waardenburg syndrome/ocular albinism
Homo sapiens (human)
DOID:8442
  • paralytic ileus
Homo sapiens (human)
DOID:3878
  • obsolete intestinal pseudo-obstruction
Homo sapiens (human)
DOID:0110409
  • retinitis pigmentosa 46
  • Aliases:
    • RP46
Homo sapiens (human)
DOID:0112147
  • retinitis pigmentosa 90
  • Aliases:
    • RP90
Homo sapiens (human)
DOID:0080005
  • bone remodeling disease
Homo sapiens (human)
DOID:6951
  • telangiectatic osteogenic sarcoma
  • Aliases:
    • Telangiectatic osteosarcoma
Homo sapiens (human)
DOID:0111352
  • D-2-hydroxyglutaric aciduria 2
  • Aliases:
    • D2HGA2
Homo sapiens (human)
DOID:369
  • olfactory neuroblastoma
  • Aliases:
    • Asthesioneuroblastoma
    • Esthesioneuroblastoma
    • Esthesioneuroepithelioma
    • Olfactory Esthesioneuroblastoma
    • paranasal sinus Olfactory neuroblastoma
Homo sapiens (human)
DOID:4853
  • pilocytic astrocytoma of cerebellum
  • Aliases:
    • Cerebellar Pilocytic astrocytoma
Homo sapiens (human)
DOID:14174
  • central neurocytoma
  • Aliases:
    • Neurolipocytoma
Homo sapiens (human)
DOID:3372
  • chondroblastic osteosarcoma
  • Aliases:
    • chondrosarcomatous Osteogenic sarcoma
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