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 351 - 375 of 4621 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism
DOID:0060253
  • scapuloperoneal myopathy
Homo sapiens (human)
DOID:0060254
  • Robinow syndrome
  • Aliases:
    • Robinow dwarfism
    • acral dysostosis with facial and genital abnormalities
    • fetal face syndrome
Homo sapiens (human)
DOID:0060255
  • rippling muscle disease 2
  • Aliases:
    • autosomal dominant limb-girdle muscular dystrophy type 1C
Homo sapiens (human)
DOID:0060256
  • Dowling-Degos disease
  • Aliases:
    • dark dot disease
    • reticular pigment anomaly of flexures
Homo sapiens (human)
DOID:0060257
  • dyschromatosis symmetrica hereditaria
  • Aliases:
    • reticulate acropigmentation of Dohi
Homo sapiens (human)
DOID:0060258
  • reticulate acropigmentation of Kitamura
  • Aliases:
    • RAPK
Homo sapiens (human)
DOID:0060260
  • ptosis
  • Aliases:
    • blepharoptosis
    • drooping eyelid
Homo sapiens (human)
DOID:0060261
  • congenital ptosis
Homo sapiens (human)
DOID:0060262
  • gallbladder disease
Homo sapiens (human)
DOID:0060263
  • porencephaly
Homo sapiens (human)
DOID:0060270
  • pontocerebellar hypoplasia type 2D
Homo sapiens (human)
DOID:0060276
  • pontocerebellar hypoplasia type 7
Homo sapiens (human)
DOID:0060277
  • pontocerebellar hypoplasia type 8
Homo sapiens (human)
DOID:0060278
  • pontocerebellar hypoplasia type 9
Homo sapiens (human)
DOID:0060280
  • primary pigmented nodular adrenocortical disease
Homo sapiens (human)
DOID:0060281
  • photosensitive epilepsy
  • Aliases:
    • photogenic epilepsy
    • photoparoxysmal response
Homo sapiens (human)
DOID:0060282
  • persistent hyperplastic primary vitreous
Homo sapiens (human)
DOID:0060283
  • peeling skin syndrome
  • Aliases:
    • deciduous skin
    • familial continuous skin peeling syndrome
    • keratosis exfoliativa congenita
    • peeling skin disease
Homo sapiens (human)
DOID:0060284
  • paroxysmal nocturnal hemoglobinuria
Homo sapiens (human)
DOID:0060285
  • parietal foramina
  • Aliases:
    • Caitlin marks
    • enlarged parietal foramina
    • hereditary cranium bifidum
Homo sapiens (human)
DOID:0060287
  • cornea plana
  • Aliases:
    • flat cornea
Homo sapiens (human)
DOID:0060288
  • omodysplasia
Homo sapiens (human)
DOID:0060291
  • oculodentodigital dysplasia
  • Aliases:
    • ODD syndrome
Homo sapiens (human)
DOID:0060292
  • X-linked chondrodysplasia punctata 1
  • Aliases:
    • chondrodystrophia calcificans congenita
Homo sapiens (human)
DOID:0060293
  • autosomal dominant chondrodysplasia punctata
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