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 5501 - 5525 of 7942 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism
DOID:14669
  • acrodysostosis
Homo sapiens (human)
DOID:0060350
  • adenine phosphoribosyltransferase deficiency
  • Aliases:
    • 2,8-dihydroxyadenine urolithiasis
    • APRT deficiency
Homo sapiens (human)
DOID:5683
  • hereditary breast ovarian cancer syndrome
  • Aliases:
    • BRCA1- and BRCA2-associated hereditary breast and ovarian cancer
    • Breast and Ovarian Cancer syndrome
    • HBOC syndrome
    • Hereditary Breast and Ovarian Cancer syndrome
    • Hereditary breast and ovarian cancer
Homo sapiens (human)
DOID:4837
  • Gorham's disease
  • Aliases:
    • Disappearing bone disease
    • Gorham disease
    • essential osteolysis
    • massive osteolysis
    • phantom bone disease
Homo sapiens (human)
DOID:5015
  • fibrolamellar carcinoma
  • Aliases:
    • Fibrolamellar hepatocellular carcinoma
    • Hepatocellular carcinoma, fibrolamellar
    • Oncocytic Hepatocellular tumor
Homo sapiens (human)
DOID:12451
  • sulfhemoglobinemia
Homo sapiens (human)
DOID:10783
  • methemoglobinemia
Homo sapiens (human)
DOID:0060358
  • multiple acyl-CoA dehydrogenase deficiency
  • Aliases:
    • MAD deficiency
    • MADD
    • electron transfer flavoprotein deficiency
    • electron transfer flavoprotein ubiquinone oxidoreductase deficiency
    • glutaric acidemia type 2
    • glutaric aciduria type 2
Homo sapiens (human)
DOID:12400
  • kleptomania
  • Aliases:
    • Pathological stealing
Homo sapiens (human)
DOID:10937
  • impulse control disorder
Homo sapiens (human)
DOID:0060098
  • osteoblastoma
Homo sapiens (human)
DOID:0050524
  • maturity-onset diabetes of the young
  • Aliases:
    • MODY
    • Mason-type diabetes
Homo sapiens (human)
DOID:14456
  • Brucella melitensis brucellosis
Homo sapiens (human)
DOID:668
  • myositis ossificans
  • Aliases:
    • Myisitis ossificans
    • Ossification - muscle
Homo sapiens (human)
DOID:13374
  • fibrodysplasia ossificans progressiva
  • Aliases:
    • Stone Man Syndrome
    • myositis ossificans progressiva
    • progressive myositis ossificans
    • progressive ossifying myositis
Homo sapiens (human)
DOID:0111253
  • neurofibromatosis 1
  • Aliases:
    • NF1
    • Peripheral Neurofibromatosis
    • Recklinghausen's neurofibromatosis
    • neurofibromatosis type I
    • von Recklinghausen Disease
Homo sapiens (human)
DOID:4647
  • trilateral retinoblastoma
Homo sapiens (human)
DOID:4648
  • familial retinoblastoma
  • Aliases:
    • Hereditary Retinoblastoma
Homo sapiens (human)
DOID:2772
  • irritant dermatitis
  • Aliases:
    • irritant contact dermatitis
    • primary irritant dermatitis
Homo sapiens (human)
DOID:3973
  • thyroid gland medullary carcinoma
  • Aliases:
    • Medullary carcinoma of the Thyroid gland
    • Ultimobranchial thyroid tumor
    • Ultimobranchial thyroid tumour
    • medullary thyroid carcinoma
Homo sapiens (human)
DOID:0050471
  • Carney complex
  • Aliases:
    • Carney Complex, Type 1
    • Carney Complex, Type 2
    • Carney Syndrome
    • Carney complex variant
    • LAMB Syndrome
    • NAME Syndrome
Homo sapiens (human)
DOID:0050523
  • adult T-cell leukemia/lymphoma
  • Aliases:
    • Adult T-cell leukemia/lymphoma (HTLV-1 positive)
    • adult T-cell leukemia
Homo sapiens (human)
DOID:12156
  • arachnoiditis
Homo sapiens (human)
DOID:9471
  • meningitis
Homo sapiens (human)
DOID:8712
  • neurofibromatosis
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: August 19, 2024