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 7251 - 7275 of 7942 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism
DOID:0110458
  • dilated cardiomyopathy 1BB
  • Aliases:
    • CMD1BB
Homo sapiens (human)
DOID:0110443
  • dilated cardiomyopathy 1B
Homo sapiens (human)
DOID:118
  • pericardial effusion
Homo sapiens (human)
DOID:11482
  • hemopericardium
  • Aliases:
    • Haemopericardium
Homo sapiens (human)
DOID:0050820
  • atrioventricular block
  • Aliases:
    • AV block
Homo sapiens (human)
DOID:0110429
  • dilated cardiomyopathy 1H
  • Aliases:
    • dilated cardiomyopathy with conduction defect
Homo sapiens (human)
DOID:12678
  • hypercalcemia
Homo sapiens (human)
DOID:2485
  • phosphorus metabolism disease
  • Aliases:
    • Phosphorus disorder
    • disorder of phosphorus metabolism
    • phosphorus metabolism disorder
Homo sapiens (human)
DOID:12679
  • nephrocalcinosis
Homo sapiens (human)
DOID:10003
  • sensorineural hearing loss
  • Aliases:
    • High Frequency Hearing Loss
    • High frequency deafness
    • Perceptive deafness
    • Perceptive hearing loss
    • Perceptive hearing loss or deafness
    • Sensorineural Deafness
    • Sensory hearing loss
    • central hearing loss
    • high-frequency hearing loss
Homo sapiens (human)
DOID:1142
  • alternating exotropia
Homo sapiens (human)
DOID:1143
  • exotropia
  • Aliases:
    • Divergent Strabismus
    • Divergent concomitant strabismus
Homo sapiens (human)
DOID:11853
  • monocular exotropia
Homo sapiens (human)
DOID:14692
  • Smith-Lemli-Opitz syndrome
  • Aliases:
    • Rutledge lethal multiple congenital anomaly syndrome
    • Smith-Opitz-Inborn syndrome
Homo sapiens (human)
DOID:0060336
  • 3-methylglutaconic aciduria
Homo sapiens (human)
DOID:10907
  • microcephaly
  • Aliases:
    • Microcephalus
    • microencephaly
Homo sapiens (human)
DOID:0060810
  • syndromic X-linked intellectual disability type 10
  • Aliases:
    • HSD10 deficiency, atypical type
    • HSD10 disease, atypical type
    • MRXS10
    • X-linked intellectual disability-choreoathetosis-abnormal behavior syndrome
    • mental retardation, X-linked syndromic 10
Homo sapiens (human)
DOID:9923
  • developmental coordination disorder
Homo sapiens (human)
DOID:4090
  • agnosia
  • Aliases:
    • Dyspraxia
    • Dyspraxia syndrome
Homo sapiens (human)
DOID:0060587
  • Noonan syndrome 9
  • Aliases:
    • NS9
Homo sapiens (human)
DOID:14796
  • Dubowitz syndrome
  • Aliases:
    • Dubowitz's syndrome
Homo sapiens (human)
DOID:0060586
  • Noonan syndrome 8
  • Aliases:
    • NS8
Homo sapiens (human)
DOID:0060767
  • autosomal dominant Robinow syndrome 3
  • Aliases:
    • DRS3
Homo sapiens (human)
DOID:0060254
  • Robinow syndrome
  • Aliases:
    • Robinow dwarfism
    • acral dysostosis with facial and genital abnormalities
    • fetal face syndrome
Homo sapiens (human)
DOID:0060765
  • autosomal dominant Robinow syndrome 2
  • Aliases:
    • DRS2
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