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 676 - 700 of 4621 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism
DOID:0060336
  • 3-methylglutaconic aciduria
Homo sapiens (human)
DOID:14692
  • Smith-Lemli-Opitz syndrome
  • Aliases:
    • Rutledge lethal multiple congenital anomaly syndrome
    • Smith-Opitz-Inborn syndrome
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: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: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:0110429
  • dilated cardiomyopathy 1H
  • Aliases:
    • dilated cardiomyopathy with conduction defect
Homo sapiens (human)
DOID:0050820
  • atrioventricular block
  • Aliases:
    • AV block
Homo sapiens (human)
DOID:118
  • pericardial effusion
Homo sapiens (human)
DOID:11482
  • hemopericardium
  • Aliases:
    • Haemopericardium
Homo sapiens (human)
DOID:0110443
  • dilated cardiomyopathy 1B
Homo sapiens (human)
DOID:0110450
  • dilated cardiomyopathy 1II
  • Aliases:
    • CMD1II
Homo sapiens (human)
DOID:0110432
  • dilated cardiomyopathy 1NN
  • Aliases:
    • CMD1NN
Homo sapiens (human)
DOID:0110435
  • dilated cardiomyopathy 1GG
  • Aliases:
    • CMD1GG
Homo sapiens (human)
DOID:0110451
  • dilated cardiomyopathy 1O
  • Aliases:
    • CMD1O
    • dilated cardiomyopathy with ventricular tachycardia
Homo sapiens (human)
DOID:0110459
  • dilated cardiomyopathy 1FF
  • Aliases:
    • CMD1FF
Homo sapiens (human)
DOID:0110454
  • dilated cardiomyopathy 1S
  • Aliases:
    • CMD1S
Homo sapiens (human)
DOID:0110428
  • dilated cardiomyopathy 1AA
  • Aliases:
    • CMD1AA
    • dilated cardiomyopathy 1AA with or without left ventricular noncompaction
Homo sapiens (human)
DOID:0110434
  • dilated cardiomyopathy 1Z
  • Aliases:
    • CMD1Z
Homo sapiens (human)
DOID:0110446
  • dilated cardiomyopathy 1W
  • Aliases:
    • CMD1W
Homo sapiens (human)
DOID:0110433
  • dilated cardiomyopathy 1E
  • Aliases:
    • CDCD2
    • CMD1E
    • dilated cardiomyopathy with conduction defect 2
    • dilated cardiomyopathy with conduction disorder and arrhythmia
Homo sapiens (human)
DOID:0110430
  • dilated cardiomyopathy 1G
  • Aliases:
    • CMD1G
Homo sapiens (human)

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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