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 3376 - 3400 of 4649 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▲
DOID:14040
  • autoimmune polyendocrine syndrome
  • Aliases:
    • Autoimmune polyglandular failure
    • Lloyd's syndrome
    • autoimmune polyendocrinopathy
Homo sapiens (human)
DOID:1405
  • primary angle-closure glaucoma
  • Aliases:
    • primary Angle Closure Glaucoma
Homo sapiens (human)
DOID:14067
  • Plasmodium falciparum malaria
  • Aliases:
    • Malaria fever, subtertian
    • falciparum malaria
    • malignant tertian fever
Homo sapiens (human)
DOID:14069
  • cerebral malaria
  • Aliases:
    • Malarial encephalitis
Homo sapiens (human)
DOID:1407
  • anterior uveitis
Homo sapiens (human)
DOID:14080
  • glucocorticoid-remediable aldosteronism
  • Aliases:
    • GRA
    • GRS
    • familial hyperaldosteronism type I
    • glucocorticoid-suppressible hyperaldosteronism
Homo sapiens (human)
DOID:14089
  • root caries
  • Aliases:
    • Cementum caries
    • Dental caries of root surface
Homo sapiens (human)
DOID:14095
  • boutonneuse fever
  • Aliases:
    • African tick typhus
    • Rickettsia conorii spotted fever
    • South African tick-bite fever
    • kenya tick typhus
    • marseilles fever
Homo sapiens (human)
DOID:14115
  • toxic shock syndrome
  • Aliases:
    • TSS
    • toxic shock
Homo sapiens (human)
DOID:14118
  • familial lipoprotein lipase deficiency
  • Aliases:
    • Fredrickson type I hyperlipoproteinemia
    • Fredrickson type I lipaemia
    • familial LPL deficiency
    • familial hyperlipoproteinemia type I
    • hypercholesterinaemic xanthomatosis
    • hyperchylomicronemia
    • mixed hyperglyceridemia
Homo sapiens (human)
DOID:14159
  • obstructive hydrocephalus
Homo sapiens (human)
DOID:1417
  • choroid disease
Homo sapiens (human)
DOID:14175
  • von Hippel-Lindau disease
  • Aliases:
    • Hippel Lindau syndrome
    • von Hippel-Lindau syndrome
Homo sapiens (human)
DOID:14176
  • selective IgG deficiency disease
  • Aliases:
    • Immunoglobin G subclass deficiency
    • Selective IgG Immunodeficiency
    • Selective Immunoglobulin G Subclass deficiency
    • Selective deficiency of IgG
    • Selective immunoglobulin G deficiency
Homo sapiens (human)
DOID:14179
  • X-linked agammaglobulinemia
  • Aliases:
    • BTK deficiency
    • Bruton agammaglobulinemia tyrosine kinase deficiency
    • Bruton disease
    • Bruton's Sex-Linked Agammaglobulinemia
    • Bruton's agammaglobulinaemia
    • Bruton's type agammaglobulinemia
    • Bruton-type agammaglobulinemia
Homo sapiens (human)
DOID:14183
  • alcoholic neuropathy
  • Aliases:
    • Alcohol-related polyneuropathy
    • Alcoholic polyneuropathy
Homo sapiens (human)
DOID:14184
  • polyneuropathy due to drug
Homo sapiens (human)
DOID:14213
  • hypophosphatasia
  • Aliases:
    • deficiency of alkaline phosphatase
Homo sapiens (human)
DOID:14218
  • dihydropyrimidine dehydrogenase deficiency
  • Aliases:
    • Dihydrouracil Dehydrogenase deficiency
    • familial pyrimidinaemia
    • thymine-uracilurea
Homo sapiens (human)
DOID:14219
  • renal tubular acidosis
Homo sapiens (human)
DOID:14221
  • abdominal obesity-metabolic syndrome 1
  • Aliases:
    • dysmetabolic syndrome X
    • metabolic syndrome X
Homo sapiens (human)
DOID:14227
  • azoospermia
Homo sapiens (human)
DOID:14228
  • oligospermia
Homo sapiens (human)
DOID:14250
  • Down syndrome
  • Aliases:
    • Complete trisomy 21 syndrome
    • Down's syndrome
    • Down's syndrome - trisomy 21
    • Downs syndrome
    • G Trisomy
    • trisomy 21 syndrome
Homo sapiens (human)
DOID:14256
  • adult-onset Still's disease
  • Aliases:
    • adult onset Still's disease
    • adult-onset Still disease
Homo sapiens (human)

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Last updated: December 9, 2024