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 4251 - 4275 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲ Source
DOID:9637
  • stomatitis
Homo sapiens (human)
DOID:3168
  • squamous cell neoplasm
  • Aliases:
    • Epidermoid cell tumor
    • squamous cell tumor
Homo sapiens (human)
DOID:0081378
  • amyotrophic lateral sclerosis type 24
Homo sapiens (human)
DOID:3498
  • pancreatic ductal adenocarcinoma
  • Aliases:
    • ductal adenocarcinoma of the pancreas
Homo sapiens (human)
DOID:2468
  • psychotic disorder
  • Aliases:
    • mental or behavioural disorder
Homo sapiens (human)
DOID:0111381
  • IVIC syndrome
  • Aliases:
    • Instituto Venezolano de Investigaciones Cientificas syndrome
    • OORS
    • Oculootoradial syndrome
    • oculo-oto-radial syndrome
    • radial ray defects, hearing impairment, external ophthalmoplegia, and thrombocytopenia
Homo sapiens (human)
DOID:0111314
  • idiopathic generalized epilepsy 13
  • Aliases:
    • EIG13
Homo sapiens (human)
DOID:0080261
  • autosomal recessive nonsyndromic deafness 106
Homo sapiens (human)
DOID:0080224
  • autosomal dominant dystrophic epidermolysis bullosa
Homo sapiens (human)
DOID:2987
  • familial mediterranean fever
  • Aliases:
    • FMF
    • benign paroxysmal peritonitis
Homo sapiens (human)
DOID:2615
  • papilloma
  • Aliases:
    • papillomatosis
Homo sapiens (human)
DOID:0050778
  • Meckel syndrome
  • Aliases:
    • Meckel-Gruber syndrome
Homo sapiens (human)
DOID:3669
  • intermittent claudication
  • Aliases:
    • Charcot's syndrome
Homo sapiens (human)
DOID:0110500
  • autosomal recessive nonsyndromic deafness 42
  • Aliases:
    • DFNB42
    • autosomal recessive deafness 42
Homo sapiens (human)
DOID:0080597
  • Kleefstra syndrome
Homo sapiens (human)
DOID:2316
  • brain ischemia
  • Aliases:
    • Ischaemic encephalopathy
    • Ischemic encephalopathy
    • cerebral ischemia
Homo sapiens (human)
DOID:0111821
  • ichthyosis follicularis-alopecia-photophobia syndrome 1
  • Aliases:
    • IFAP syndrome 1
    • IFAP syndrome 1 with or without BRESHECK syndrome
    • ichthyosis follicularis-atrichia-photophobia syndrome 1
Homo sapiens (human)
DOID:3192
  • neurilemmoma
  • Aliases:
    • Psammomatous schwannoma
    • schwannoma
Homo sapiens (human)
DOID:0090130
  • cortical dysplasia-focal epilepsy syndrome
  • Aliases:
    • CDFE syndrome
    • CDFES
    • PTHSL1
    • Pitt-Hopkins-like syndrome-1
Homo sapiens (human)
DOID:615
  • leukopenia
  • Aliases:
    • Leucopenia
Homo sapiens (human)
DOID:12029
  • sympathetic ophthalmia
  • Aliases:
    • Sympathetic uveitis
Homo sapiens (human)
DOID:12783
  • migraine without aura
  • Aliases:
    • common migraine
Homo sapiens (human)
DOID:0070056
  • autosomal dominant intellectual developmental disorder 26
  • Aliases:
    • MRD26
    • autosomal dominant mental retardation 26
    • autosomal dominant non-syndromic intellectual disability 26
Homo sapiens (human)
DOID:2277
  • gonadal disease
Homo sapiens (human)
DOID:10966
  • lipoid nephrosis
  • Aliases:
    • Minimal Change Glomerulonephritis
    • Minimal change disease
    • Nephrotic syndrome with lesion of minimal change glomerulonephritis
    • Nephrotic syndrome with lesion of minimal change nephrotic syndrome
Homo sapiens (human)

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024