GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 7201 - 7225 of 7942 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism
DOID:0110111
  • atrial heart septal defect 6
  • Aliases:
    • ASD6
    • atrial septal defect 6
Homo sapiens (human)
DOID:1882
  • atrial heart septal defect
  • Aliases:
    • atrial septal defect
    • atrioseptal defect
    • auricular septal defect
    • congenital atrial septal defect
    • interatrial septal defect
    • interauricular septal defect
Homo sapiens (human)
DOID:0110107
  • atrial heart septal defect 2
  • Aliases:
    • ASD2
    • atrial septal defect 2
Homo sapiens (human)
DOID:0110113
  • atrial heart septal defect 8
  • Aliases:
    • ASD8
    • atrial septal defect 8
Homo sapiens (human)
DOID:0110108
  • atrial heart septal defect 3
  • Aliases:
    • ASD3
    • atrial septal defect 3
Homo sapiens (human)
DOID:0110112
  • atrial heart septal defect 7
  • Aliases:
    • ASD with or without atrioventricular conduction defects
    • atrial septal defect 7, with or without AV conduction defects
    • atrial septal defect-atrioventricular conduction defects syndrome
Homo sapiens (human)
DOID:9080
  • macroglobulinemia
  • Aliases:
    • primary macroglobulinemia
Homo sapiens (human)
DOID:0050747
  • obsolete lymphoplasmacytic lymphoma
Homo sapiens (human)
DOID:13372
  • alpha 1-antitrypsin deficiency
  • Aliases:
    • AAT deficiency
Homo sapiens (human)
DOID:0060679
  • catecholaminergic polymorphic ventricular tachycardia 5
  • Aliases:
    • CVPT5
Homo sapiens (human)
DOID:0060677
  • catecholaminergic polymorphic ventricular tachycardia 3
  • Aliases:
    • CVPT3
Homo sapiens (human)
DOID:0060676
  • catecholaminergic polymorphic ventricular tachycardia 2
  • Aliases:
    • CVPT2
Homo sapiens (human)
DOID:0060678
  • catecholaminergic polymorphic ventricular tachycardia 4
  • Aliases:
    • CVPT4
Homo sapiens (human)
DOID:0060674
  • catecholaminergic polymorphic ventricular tachycardia
Homo sapiens (human)
DOID:0060675
  • catecholaminergic polymorphic ventricular tachycardia 1
  • Aliases:
    • CVPT1
    • arrhythmogenic right ventricular dysplasia 2
Homo sapiens (human)
DOID:0060295
  • complement component 2 deficiency
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)

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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