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 1176 - 1200 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:4336
  • tinea favosa
  • Aliases:
    • favus
Homo sapiens (human)
DOID:1596
  • depressive disorder
  • Aliases:
    • mental depression
Homo sapiens (human)
DOID:14040
  • autoimmune polyendocrine syndrome
  • Aliases:
    • Autoimmune polyglandular failure
    • Lloyd's syndrome
    • autoimmune polyendocrinopathy
Homo sapiens (human)
DOID:1967
  • leiomyosarcoma
  • Aliases:
    • Leiomyosarcomas
Homo sapiens (human)
DOID:0111146
  • acquired von Willebrand syndrome
  • Aliases:
    • AVWS
Homo sapiens (human)
DOID:2426
  • gangliocytoma
  • Aliases:
    • gangliocytoma of central nervous system
Homo sapiens (human)
DOID:0060810
  • syndromic X-linked intellectual disability type 10
  • Aliases:
    • HSD10 deficiency, atypical type
    • HSD10 disease, atypical type
    • MRXS10
    • X-linked intellectual disability-choreoathetosis-abnormal behavior syndrome
    • mental retardation, X-linked syndromic 10
Homo sapiens (human)
DOID:3500
  • gallbladder adenocarcinoma
  • Aliases:
    • adenocarcinoma of the gallbladder
Homo sapiens (human)
DOID:3572
  • intracranial sinus thrombosis
Homo sapiens (human)
DOID:11328
  • schizophreniform disorder
Homo sapiens (human)
DOID:1068
  • juvenile glaucoma
  • Aliases:
    • Glaucoma of childhood
Homo sapiens (human)
DOID:0090088
  • hypogonadotropic hypogonadism 24 without anosmia
  • Aliases:
    • isolated follicle-stimulating hormone deficiency
Homo sapiens (human)
DOID:0080216
  • duodenal atresia
Homo sapiens (human)
DOID:0111756
  • Leber hereditary optic neuropathy with demyelinating disease of CNS
Homo sapiens (human)
DOID:0110199
  • Charcot-Marie-Tooth disease dominant intermediate C
  • Aliases:
    • CMTDIC
    • Charcot-Marie-Tooth neuropathy dominant intermediate C
    • DI-CMTC
    • autosomal dominant intermediate Charcot-Marie-Tooth disease type C
Homo sapiens (human)
DOID:2388
  • renal artery disease
  • Aliases:
    • renal vascular disease
    • vascular disorder of kidney
Homo sapiens (human)
DOID:0080491
  • cerebral cavernous malformation 1
Homo sapiens (human)
DOID:0050819
  • obsolete Matthew-Wood syndrome
Homo sapiens (human)
DOID:2750
  • glycogen storage disease IV
  • Aliases:
    • Amylopectinosis
    • Branching-transferase deficiency glycogenosis
    • Glycogen storage disease 4
    • Glycogen storage disease, type IV
    • brancher deficiency glycogenosis
    • deficiency of 1,4-alpha-glucan branching enzyme
Homo sapiens (human)
DOID:303
  • substance-related disorder
Homo sapiens (human)
DOID:1875
  • impotence
  • Aliases:
    • Sexual impotence
    • erectile dysfunction
Homo sapiens (human)
DOID:10974
  • oophoritis
Homo sapiens (human)
DOID:4780
  • anti-basement membrane glomerulonephritis
  • Aliases:
    • anti-GBM glomerulonephritis
Homo sapiens (human)
DOID:6432
  • pulmonary hypertension
Homo sapiens (human)
DOID:2346
  • monoclonal paraproteinemia
  • Aliases:
    • Monoclonal paraproteinaemia
Homo sapiens (human)

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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