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 2926 - 2950 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼
DOID:589
  • congenital hemolytic anemia
  • Aliases:
    • congenital hemolytic anaemia
    • hereditary hemolytic anaemia
    • hereditary hemolytic anemia
Homo sapiens (human)
DOID:0050816
  • urofacial syndrome
  • Aliases:
    • Ochoa syndrome
    • hydronephrosis with peculiar facial expression
Homo sapiens (human)
DOID:0110572
  • autosomal dominant nonsyndromic deafness 49
  • Aliases:
    • DFNA49
    • autosomal dominant deafness 49
Homo sapiens (human)
DOID:0111633
  • congenital sucrase-isomaltase deficiency
  • Aliases:
    • CSID
    • SI deficiency
    • congenital sucrase-isomaltose malabsorption
    • congenital sucrose intolerance
    • disaccharide intolerance
Homo sapiens (human)
DOID:0110303
  • autosomal dominant limb-girdle muscular dystrophy type 1H
  • Aliases:
    • LGMD1H
    • muscular dystrophy limb-girdle type 1H
Homo sapiens (human)
DOID:1063
  • interstitial nephritis
  • Aliases:
    • renal tubulo-interstitial disease
Homo sapiens (human)
DOID:2527
  • nephrosis
Homo sapiens (human)
DOID:3969
  • thyroid gland papillary carcinoma
  • Aliases:
    • Papillary carcinoma of the Thyroid gland
Homo sapiens (human)
DOID:3846
  • adamantinous craniopharyngioma
  • Aliases:
    • Adamantinous Rathke's Pouch tumor
    • craniopharyngioma, adamantinomatous
Homo sapiens (human)
DOID:10423
  • acute pericementitis
  • Aliases:
    • acute periodontitis
Homo sapiens (human)
DOID:679
  • basal ganglia disease
Homo sapiens (human)
DOID:9828
  • neonatal abstinence syndrome
  • Aliases:
    • Drug withdrawal syndrome in newborn
Homo sapiens (human)
DOID:0050476
  • Barth syndrome
  • Aliases:
    • 3-methylglutaconicaciduria type 2
    • 3-methylglutaconicaciduria type II
    • MGA Type 2
    • MGA type II
Homo sapiens (human)
DOID:5389
  • oxyphilic adenoma
  • Aliases:
    • Follicular adenoma, oxyphilic cell
    • Oncocytoma
Homo sapiens (human)
DOID:0080753
  • keratosis follicularis spinulosa decalvans
Homo sapiens (human)
DOID:0110058
  • amelogenesis imperfecta type 1E
  • Aliases:
    • AIH1
    • X-linked amelogenesis imperfecta 1
    • X-linked amelogenesis imperfecta hypoplastic/hypomaturation 1
    • amelogenesis imperfecta hypomaturationtype with snow-capped teeth
    • amelogenesis imperfecta type IE
Homo sapiens (human)
DOID:0110478
  • autosomal recessive nonsyndromic deafness 20
  • Aliases:
    • DFNB20
    • autosomal recessive deafness 20
Homo sapiens (human)
DOID:9884
  • muscular dystrophy
Homo sapiens (human)
DOID:12375
  • bronchopneumonia
  • Aliases:
    • Chest infection - bronchopneumonia
    • bronchial pneumonia
    • lobular pneumonia
Homo sapiens (human)
DOID:0111248
  • cerebrocostomandibular syndrome
  • Aliases:
    • CCM syndrome
    • CCMS
    • cerebro-costo-mandibular syndrome
    • rib gap defects with micrognathia
Homo sapiens (human)
DOID:12140
  • Chagas disease
  • Aliases:
    • Chagas' disease
    • chagas' disease with digestive system involvement
    • chagas' disease with nervous system involvement
    • chagas' disease with other organ involvement
Homo sapiens (human)
DOID:0110728
  • neuronal ceroid lipofuscinosis 5
  • Aliases:
    • CLN5
    • neuronal ceroid lipofuscinosis 5 variable age of onset
Homo sapiens (human)
DOID:5442
  • eccrine acrospiroma
  • Aliases:
    • Eccrine hidradenoma
    • Eccrine hidradenoma of skin
    • Poroma
Homo sapiens (human)
DOID:0111341
  • primary failure of tooth eruption
  • Aliases:
    • PFE
    • dental noneruption
    • familial posterior openbite malocclusion
    • nonsyndromic primary failure of eruption
    • primary retention of teeth
    • unerupted second primary molar
Homo sapiens (human)
DOID:14735
  • hereditary angioedema
  • Aliases:
    • HANE
    • Hereditary angioneurotic edema
Homo sapiens (human)

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Last updated: August 19, 2024