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 1351 - 1375 of 4621 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism
DOID:0111141
  • delayed sleep phase syndrome
  • Aliases:
    • DSPD
Homo sapiens (human)
DOID:0060282
  • persistent hyperplastic primary vitreous
Homo sapiens (human)
DOID:0111234
  • congenital muscular dystrophy-dystroglycanopathy A7
  • Aliases:
    • MDDGA7
    • Walker-Warburg syndrome or muscle-eye-brain disease ISPD-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A7
Homo sapiens (human)
DOID:0111231
  • congenital muscular dystrophy-dystroglycanopathy type A8
  • Aliases:
    • MDDGA8
    • Walker-Warburg syndrome or muscle-eye-brain disease GTDC2-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A8
Homo sapiens (human)
DOID:0070430
  • combined oxidative phosphorylation deficiency 57
  • Aliases:
    • COXPD57
Homo sapiens (human)
DOID:3783
  • Coffin-Lowry syndrome
Homo sapiens (human)
DOID:14464
  • neuroleptic malignant syndrome
Homo sapiens (human)
DOID:0080108
  • myoglobinuria
Homo sapiens (human)
DOID:0060645
  • chronic recurrent multifocal osteomyelitis
  • Aliases:
    • CRMO
    • chronic multifocal osteomyelitis
Homo sapiens (human)
DOID:4051
  • alveolar rhabdomyosarcoma
  • Aliases:
    • alveolar childhood rhabdomyosarcoma
Homo sapiens (human)
DOID:4253
  • melorheostosis
Homo sapiens (human)
DOID:0060046
  • aphasia
Homo sapiens (human)
DOID:5693
  • adult liposarcoma
Homo sapiens (human)
DOID:5695
  • childhood liposarcoma
  • Aliases:
    • pediatric liposarcoma
Homo sapiens (human)
DOID:0050730
  • coenzyme Q10 deficiency disease
  • Aliases:
    • COENZYME Q10 DEFICIENCY, PRIMARY
Homo sapiens (human)
DOID:0070238
  • primary coenzyme Q10 deficiency 1
  • Aliases:
    • COQ10D1
    • CoQ deficiency 1
    • CoQ10 deficiency, primary, 1
    • coenzyme Q deficiency 1
    • ubiquinone deficiency 1
Homo sapiens (human)
DOID:0110629
  • Wolfram syndrome 1
  • Aliases:
    • DIDMOAD
    • WFS1
    • diabetes mellitus AND insipidus with optic atrophy AND deafness
Homo sapiens (human)
DOID:10632
  • Wolfram syndrome
  • Aliases:
    • WFS
Homo sapiens (human)
DOID:10646
  • schizotypal personality disorder
Homo sapiens (human)
DOID:0090054
  • episodic kinesigenic dyskinesia 2
Homo sapiens (human)
DOID:0060165
  • Kleine-Levin syndrome
Homo sapiens (human)
DOID:0050158
  • desquamative interstitial pneumonia
  • Aliases:
    • RBILD
    • familial desquamative interstitial pneumonitis
    • respiratory bronchiolitis-associated interstitial lung disease
Homo sapiens (human)
DOID:9427
  • hypertensive encephalopathy
Homo sapiens (human)
DOID:0080169
  • tricuspid atresia
Homo sapiens (human)
DOID:0111343
  • lateral meningocele syndrome
  • Aliases:
    • Lehman syndrome
Homo sapiens (human)

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Last updated: August 19, 2024