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 5326 - 5350 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼
DOID:9952
  • acute lymphoblastic leukemia
  • Aliases:
    • ALL
    • acute lymphoblastic leukaemia
    • acute lymphocytic leukaemia
    • precursor lymphoblastic lymphoma/leukemia
Homo sapiens (human)
DOID:11201
  • parathyroid gland disease
  • Aliases:
    • disease of parathyroid glands
Homo sapiens (human)
DOID:0110235
  • cataract 2 multiple types
  • Aliases:
    • CTRCT2
    • cataract 2 multiple types with or without microcornea
Homo sapiens (human)
DOID:10348
  • blepharophimosis
Homo sapiens (human)
DOID:1824
  • status epilepticus
  • Aliases:
    • Grand mal status
Homo sapiens (human)
DOID:2883
  • prostatic adenoma
  • Aliases:
    • adenoma - prostate
    • adenoma of prostate
    • benign adenoma of prostate
    • prostate adenoma
Homo sapiens (human)
DOID:0050453
  • lissencephaly
Homo sapiens (human)
DOID:0060294
  • cold-induced sweating syndrome
  • Aliases:
    • Crisponi syndrome
    • Sohar-Crisponi syndrome
Homo sapiens (human)
DOID:9602
  • necrotizing fasciitis
Homo sapiens (human)
DOID:10393
  • secondary hypertrophic osteoarthropathy
  • Aliases:
    • Bamberger-Marie disease
    • HPOA - hypertrophic pulmonary osteoarthropathy
    • Marie Bamberger disease
    • hypertrophic pulmonary osteoarthropathy
Homo sapiens (human)
DOID:14499
  • Fabry disease
  • Aliases:
    • Alpha-galactosidase A deficiency
    • Angiokeratoma Corporis Diffusum
    • Fabry Disease, Cardiac Variant
    • Fabry's disease
    • alpha galactosidase deficiency
    • deficiency of melibiase
Homo sapiens (human)
DOID:5485
  • synovial sarcoma
Homo sapiens (human)
DOID:2862
  • glucosephosphate dehydrogenase deficiency
  • Aliases:
    • Glucose-6-phosphate dehydrogenase deficiency
    • deficiency of G-6PD
Homo sapiens (human)
DOID:3857
  • large cell medulloblastoma
  • Aliases:
    • Anaplastic medulloblastoma
Homo sapiens (human)
DOID:8970
  • subacute sclerosing panencephalitis
  • Aliases:
    • Immunosuppressive measles encephalitis
    • Van Bogaert's sclerosing leukoencephalitis
    • subacute sclerosing leukoencephalopathy
Homo sapiens (human)
DOID:5223
  • infertility
Homo sapiens (human)
DOID:5998
  • microglandular adenosis
  • Aliases:
    • Adenosis - breast
    • Adenosis of the breast
Homo sapiens (human)
DOID:0060162
  • dentatorubral-pallidoluysian atrophy
  • Aliases:
    • DRPLA
    • Haw River Syndrome
    • Naito-Oyanagi disease
Homo sapiens (human)
DOID:0060311
  • adenoid hypertrophy
  • Aliases:
    • adenoidal hypertrophy
    • enlarged adenoids
Homo sapiens (human)
DOID:13375
  • temporal arteritis
  • Aliases:
    • Horton's disease
    • giant cell arteritis
Homo sapiens (human)
DOID:13382
  • megaloblastic anemia
  • Aliases:
    • Grasbeck-Imerslund syndrome
    • Imerslund-Grasbeck syndrome
    • MGA1 Norwegian type
    • RH-MGA1
    • megaloblastic anaemia
    • recessive hereditary megaloblastic anaemia 1
    • recessive hereditary megaloblastic anemia 1
Homo sapiens (human)
DOID:0112127
  • HRPT-related hyperuricemia
  • Aliases:
    • HPRT deficiency, grade I
    • HPRT partial deficiency
    • HPRT-related gout
    • HPRT-related hyperuricemia
    • HPRT1 partial deficiency
    • Kelley-Seegmiller syndrome
    • hypoxanthine guanine phosphoribosyltransferase 1 partial deficiency
    • hypoxanthine guanine phosphoribosyltransferase deficiency, grade I
    • hypoxanthine guanine phosphoribosyltransferase partial deficiency
Homo sapiens (human)
DOID:0111239
  • congenital muscular dystrophy-dystroglycanopathy type A10
  • Aliases:
    • MDDGA10
    • Walker-Warburg syndrome or muscle-eye-brain disease, TMEM5-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A10
Homo sapiens (human)
DOID:4972
  • myelodysplastic/myeloproliferative neoplasm
  • Aliases:
    • Myeloproliferative/Myelodysplastic syndromes
    • myelodysplastic myeloproliferative cancer
Homo sapiens (human)
DOID:0080005
  • bone remodeling disease
Homo sapiens (human)

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Last updated: August 19, 2024