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 1001 - 1025 of 4621 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism
DOID:0080762
  • autosomal recessive limb-girdle muscular dystrophy type 2Z
  • Aliases:
    • limb-girdle muscular dystrophy 21
Homo sapiens (human)
DOID:0080768
  • pyridoxine-dependent epilepsy
Homo sapiens (human)
DOID:0080784
  • urinary tract infection
  • Aliases:
    • UTI
Homo sapiens (human)
DOID:0080797
  • nasal type extranodal NK/T-cell lymphoma
Homo sapiens (human)
DOID:0080821
  • exercise-induced bronchoconstriction
  • Aliases:
    • exercise-induced asthma
Homo sapiens (human)
DOID:0080822
  • aspirin-induced respiratory disease
  • Aliases:
    • aspirin-sensitive asthma
Homo sapiens (human)
DOID:0080844
  • omodysplasia 1
Homo sapiens (human)
DOID:0080855
  • Parkinsonism
Homo sapiens (human)
DOID:0080886
  • vitamin D-dependent rickets type 1A
Homo sapiens (human)
DOID:0080887
  • vitamin D-dependent rickets type 1B
Homo sapiens (human)
DOID:0080899
  • lung pleomorphic carcinoma
Homo sapiens (human)
DOID:0080909
  • castration-resistant prostate carcinoma
Homo sapiens (human)
DOID:0080923
  • bilateral parasagittal parieto-occipital polymicrogyria
  • Aliases:
    • bilateral temporooccipital polymicrogyria
Homo sapiens (human)
DOID:0080932
  • primary localized cutaneous amyloidosis 3
  • Aliases:
    • Amyloidosis cutis dyschromica
Homo sapiens (human)
DOID:0080941
  • acquired angioedema
Homo sapiens (human)
DOID:0080950
  • alopecia-mental retardation syndrome 4
Homo sapiens (human)
DOID:0080952
  • AMED syndrome
  • Aliases:
    • AMEDS
Homo sapiens (human)
DOID:0080998
  • acute necrotizing pancreatitis
Homo sapiens (human)
DOID:0081001
  • Cowden syndrome 5
Homo sapiens (human)
DOID:0081002
  • Cowden syndrome 6
Homo sapiens (human)
DOID:0081023
  • retinal cone dystrophy 4
Homo sapiens (human)
DOID:0081097
  • Rafiq syndrome
  • Aliases:
    • MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15
Homo sapiens (human)
DOID:0081120
  • Graves ophthalmopathy
  • Aliases:
    • Graves orbitopathy
    • Thyroid associated ophthalmopathy
    • thyroid eye disease
Homo sapiens (human)
DOID:0081122
  • Catel Manzke syndrome
  • Aliases:
    • Hyperphalangy-clinodactyly of index finger with Pierre Robin syndrome
    • Micrognathia digital syndrome
Homo sapiens (human)
DOID:0081168
  • HMG-CoA synthase 2 deficiency
  • Aliases:
    • 3-hydroxy-3-methylglutaryl-CoA synthase-2 deficiency
Homo sapiens (human)

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Last updated: August 19, 2024