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 4976 - 5000 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:96
  • staphyloenterotoxemia
  • Aliases:
    • Staphylococcal food poisoning
    • Staphylococcal toxaemia due to food
    • staphyloenterotoxicosis
Homo sapiens (human)
DOID:1428
  • endocrine pancreas disease
Homo sapiens (human)
DOID:12306
  • vitiligo
Homo sapiens (human)
DOID:0111083
  • Fanconi anemia complementation group D2
  • Aliases:
    • FA4
    • FAD2
    • FANCD2
    • Fanconi pancytopenia type 4
Homo sapiens (human)
DOID:2800
  • acute interstitial pneumonia
  • Aliases:
    • AIP
    • Hamman-Rich disease
    • Hamman-Rich syndrome
    • Idiopathic pulmonary fibrosis, acute fatal form
    • accelerated interstitial pneumonia
    • acute interstitial pneumonitis
Homo sapiens (human)
DOID:1540
  • parathyroid carcinoma
  • Aliases:
    • Parathyroid gland neoplasm
    • carcinoma of Parathyroid gland
    • malignant neoplasm of parathyroid gland
    • malignant neoplasm of the Parathyroid
    • malignant tumor of parathyroid gland
    • neoplasm of parathyroid gland
    • parathyroid gland cancer
    • parathyroid neoplasm
Homo sapiens (human)
DOID:0060537
  • mitochondrial complex II deficiency
  • Aliases:
    • isolated mitochondrial respiratory chain complex II deficiency
    • isolated succinate-CoQ reductase deficiency
    • isolated succinate-coenzyme Q reductase deficiency
    • isolated succinate-ubiquinone reductase deficiency
Homo sapiens (human)
DOID:12858
  • Huntington's disease
  • Aliases:
    • HD
    • Huntington disease
    • Huntington's chorea
Homo sapiens (human)
DOID:7614
  • meninges sarcoma
  • Aliases:
    • Meningeal sarcoma
    • sarcoma of meninges
Homo sapiens (human)
DOID:0110793
  • hereditary spastic paraplegia 41
  • Aliases:
    • SPG41
    • autosomal dominant spastic paraplegia 41
    • autosomal dominant spastic paraplegia type 41
Homo sapiens (human)
DOID:657
  • adenoma
  • Aliases:
    • acinar cell adenoma
    • acinic cell adenoma
    • adenomas
Homo sapiens (human)
DOID:0110509
  • autosomal recessive nonsyndromic deafness 53
  • Aliases:
    • DFNB53
    • autosomal recessive deafness 53
Homo sapiens (human)
DOID:0060582
  • Noonan syndrome 4
  • Aliases:
    • NS4
Homo sapiens (human)
DOID:12799
  • mucopolysaccharidosis II
  • Aliases:
    • Hunter syndrome
    • Hunter's syndrome
    • MPS II - Hunter syndrome
    • Mucopolysaccharidosis, MPS-II
    • deficiency of iduronate-2-sulphatase
Homo sapiens (human)
DOID:305
  • carcinoma
  • Aliases:
    • epithelial cancer
    • epithelioma
    • malignant Epithelioma
Homo sapiens (human)
DOID:0110548
  • autosomal dominant nonsyndromic deafness 17
  • Aliases:
    • DFNA17
    • autosomal dominant deafness 17
Homo sapiens (human)
DOID:3030
  • mucinous adenocarcinoma
  • Aliases:
    • Mucin-Secreting adenocarcinoma
    • Mucin-Secreting carcinoma
    • Mucous carcinoma
    • Pseudomyxoma peritonei with unknown primary site
    • mucin-producing adenocarcinoma
Homo sapiens (human)
DOID:13364
  • obsolete chronobiology disease
Homo sapiens (human)
DOID:3756
  • protein C deficiency
Homo sapiens (human)
DOID:4336
  • tinea favosa
  • Aliases:
    • favus
Homo sapiens (human)
DOID:10300
  • Raynaud disease
  • Aliases:
    • Raynaud's disease
    • Raynaud's syndrome
Homo sapiens (human)
DOID:0060245
  • Mast syndrome
  • Aliases:
    • SPG21
    • autosomal recessive spastic paraplegia 21
    • autosomal recessive spastic paraplegia type 21
    • hereditary spastic paraplegia 21
Homo sapiens (human)
DOID:12347
  • osteogenesis imperfecta
  • Aliases:
    • Lobstein's syndrome
    • Osteopsathyrosis
    • Vrolik's disease
    • brittle bone disease
Homo sapiens (human)
DOID:0080467
  • developmental and epileptic encephalopathy 2
  • Aliases:
    • DEE2
    • EIEE2
    • X-linked infantile spasm syndrome 2
    • early infantile epileptic encephalopathy 2
Homo sapiens (human)
DOID:10113
  • trypanosomiasis
Homo sapiens (human)

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Last updated: August 19, 2024