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 October 9, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 4601 - 4625 of 4649 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism Source
DOID:0050440
  • familial partial lipodystrophy
  • Aliases:
    • Dunnigan Syndrome
    • Koberling-Dunnigan Syndrome
Homo sapiens (human)
DOID:0050439
  • Usher syndrome
Homo sapiens (human)
DOID:0050437
  • Danon disease
  • Aliases:
    • ANTOPOL DISEASE
    • PSEUDOGLYCOGENOSIS II
Homo sapiens (human)
DOID:0050436
  • mulibrey nanism
  • Aliases:
    • MUL
    • Mulibrey growth disorder
    • Muscle-Liver-Brain-Eye Nanism
    • PERICARDIAL CONSTRICTION AND GROWTH FAILURE
    • Perheentupa Syndrome
Homo sapiens (human)
DOID:0050433
  • fatal familial insomnia
Homo sapiens (human)
DOID:0050432
  • Asperger syndrome
Homo sapiens (human)
DOID:0050431
  • arrhythmogenic right ventricular cardiomyopathy
  • Aliases:
    • ARVC
    • ARVC cardiomyopathy
    • ARVD
    • arrhythmogenic right ventricular dysplasia
    • arrhythmogenic right ventricular dysplasia/cardiomyopathy
    • right ventricular ACM
Homo sapiens (human)
DOID:0050430
  • multiple endocrine neoplasia type 2A
  • Aliases:
    • MEN2A
    • Sipple syndrome
    • multiple endocrine neoplasia II
Homo sapiens (human)
DOID:0050429
  • Hailey-Hailey disease
  • Aliases:
    • BENIGN CHRONIC PEMPHIGUS
    • Pemphigus, Benign Familial
Homo sapiens (human)
DOID:0050427
  • xeroderma pigmentosum
Homo sapiens (human)
DOID:0050426
  • Stevens-Johnson syndrome
Homo sapiens (human)
DOID:0050425
  • restless legs syndrome
  • Aliases:
    • WED
    • Willis-Ekbom disease
    • Wittmaack-Ekbom syndrome
Homo sapiens (human)
DOID:0050424
  • familial adenomatous polyposis
  • Aliases:
    • adenomatous polyposis of the colon
Homo sapiens (human)
DOID:0050419
  • complement factor I deficiency
  • Aliases:
    • C3 INACTIVATOR DEFICIENCY
    • COMPLEMENT COMPONENT 3 INACTIVATOR DEFICIENCY
Homo sapiens (human)
DOID:0050387
  • nonpapillary renal cell carcinoma
Homo sapiens (human)
DOID:0050340
  • opportunistic bacterial infectious disease
Homo sapiens (human)
DOID:0050338
  • primary bacterial infectious disease
Homo sapiens (human)
DOID:0050336
  • hypophosphatemia
Homo sapiens (human)
DOID:0050331
  • lacrimoauriculodentodigital syndrome 1
  • Aliases:
    • LEVY-HOLLISTER SYNDROME
    • Lacrimo-auriculo-dento-digital syndrome 1
Homo sapiens (human)
DOID:0050328
  • congenital hypothyroidism
Homo sapiens (human)
DOID:0050214
  • Lambert-Eaton myasthenic syndrome
  • Aliases:
    • Eaton-Lambert syndrome
    • LEMS
    • Lambert-Eaton syndrome
Homo sapiens (human)
DOID:0050211
  • swine influenza
Homo sapiens (human)
DOID:0050200
  • Korean hemorrhagic fever
Homo sapiens (human)
DOID:0050185
  • erythema multiforme
Homo sapiens (human)
DOID:0050175
  • tick-borne encephalitis
  • Aliases:
    • Central European encephalitis
    • Far Eastern TBE
    • Russian spring-summer encephalitis
    • Siberian tick-borne encephalitis
    • Taiga encephalitis
    • Western European tick-borne encephalitis
    • west-Siberian encephalitis
Homo sapiens (human)

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Last updated: December 9, 2024