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 1201 - 1225 of 4621 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism
DOID:11400
  • pyelonephritis
Homo sapiens (human)
DOID:1063
  • interstitial nephritis
  • Aliases:
    • renal tubulo-interstitial disease
Homo sapiens (human)
DOID:2744
  • pyelitis
Homo sapiens (human)
DOID:0090053
  • episodic kinesigenic dyskinesia 1
  • Aliases:
    • Paroxysmal kinesigenic choreoathetosis
Homo sapiens (human)
DOID:2746
  • glycogen storage disease V
  • Aliases:
    • Glycogen storage disease 5
    • Glycogen storage disease, type V
    • McArdle's disease
    • glycogen storage disease type V
    • myophosphorylase deficiency
Homo sapiens (human)
DOID:13001
  • carotid stenosis
  • Aliases:
    • Carotid artery stenosis
    • Stenosis, carotid artery
Homo sapiens (human)
DOID:3410
  • carotid artery thrombosis
Homo sapiens (human)
DOID:10554
  • meningoencephalitis
Homo sapiens (human)
DOID:0070161
  • hereditary sensory and autonomic neuropathy type 2
  • Aliases:
    • HSAN2
    • hereditary sensory and autonomic neuropathy type II
Homo sapiens (human)
DOID:1926
  • Gaucher's disease
  • Aliases:
    • Gaucher disease
    • acid beta-glucosidase deficiency
    • glocucerebrosidase deficiency
    • glucosylceramide beta-glucosidase deficiency
    • kerasin thesaurismosis
Homo sapiens (human)
DOID:820
  • myocarditis
  • Aliases:
    • Myocardial inflammation
Homo sapiens (human)
DOID:0050651
  • atrioventricular septal defect
  • Aliases:
    • AVCD
    • AVSD
    • ECD
    • atrioventricular canal defect
    • endocardial cushion defect
Homo sapiens (human)
DOID:0060000
  • infective endocarditis
Homo sapiens (human)
DOID:0060257
  • dyschromatosis symmetrica hereditaria
  • Aliases:
    • reticulate acropigmentation of Dohi
Homo sapiens (human)
DOID:10024
  • migraine with aura
  • Aliases:
    • classic migraine
Homo sapiens (human)
DOID:483
  • cavernous hemangioma
  • Aliases:
    • Cavernoma
    • Cavernous haemangioma
Homo sapiens (human)
DOID:2725
  • capillary hemangioma
  • Aliases:
    • Capillary haemangioma
    • Congenital vascular hamartoma
    • Congenital vascular naevus
    • Infantile hemangioma
    • Juvenile hemangioma
    • Strawberry haemangioma
    • Strawberry nevus
    • Strawberry nevus of skin
    • cellular hemangioma of Infancy
Homo sapiens (human)
DOID:4028
  • angioma serpiginosum
  • Aliases:
    • Angioma serpiginosum of skin
Homo sapiens (human)
DOID:841
  • extrinsic allergic alveolitis
  • Aliases:
    • alveolitis
    • hypersensitivity pneumonitis
Homo sapiens (human)
DOID:0080205
  • CAKUT
  • Aliases:
    • Congenital anomalies of the kidney and urinary tract
    • Renal or urinary tract malformation
Homo sapiens (human)
DOID:9675
  • pulmonary emphysema
Homo sapiens (human)
DOID:854
  • collagen disease
  • Aliases:
    • collagen disorder
Homo sapiens (human)
DOID:0080491
  • cerebral cavernous malformation 1
Homo sapiens (human)
DOID:11111
  • hydronephrosis
Homo sapiens (human)
DOID:11123
  • Henoch-Schoenlein purpura
  • Aliases:
    • Allergic purpura
    • Autoimmune purpura
    • Henoch-Sch?nlein purpura
    • Henoch-Sch@nlein purpura
    • Henoch-Scholein purpura
    • Henoch-Schonlein Purpura
    • Purpura, autoimmune
Homo sapiens (human)

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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