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 1601 - 1625 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:8826
  • colon carcinoma in situ
  • Aliases:
    • carcinoma in situ of colon
    • stage 0 Colonic carcinoma
Homo sapiens (human)
DOID:6245
  • renal oncocytoma
  • Aliases:
    • Oncocytoma of kidney
    • renal epithelial Oncocytic tumor
Homo sapiens (human)
DOID:0060224
  • atrial fibrillation
  • Aliases:
    • A-fib
    • AFib
Homo sapiens (human)
DOID:0110390
  • retinitis pigmentosa 1
  • Aliases:
    • RP1
Homo sapiens (human)
DOID:0050625
  • biliary tract benign neoplasm
  • Aliases:
    • extrahepatic bile duct neoplasm
    • neoplasm of extrahepatic bile ducts
    • tumor of the extrahepatic bile duct
Homo sapiens (human)
DOID:4306
  • radiculopathy
  • Aliases:
    • pinched nerve
Homo sapiens (human)
DOID:0050570
  • congenital disorder of glycosylation type I
Homo sapiens (human)
DOID:0060463
  • NUT midline carcinoma
  • Aliases:
    • nuclear protein in testis midline carcinoma
Homo sapiens (human)
DOID:0110783
  • hereditary spastic paraplegia 32
  • Aliases:
    • SPG32
    • autosomal recessive spastic paraplegia 32
    • autosomal recessive spastic paraplegia type 32
Homo sapiens (human)
DOID:3829
  • pituitary adenoma
  • Aliases:
    • adenoma of the Pituitary gland
Homo sapiens (human)
DOID:10460
  • nasopharyngitis
  • Aliases:
    • chronic nasopharyngitis
Homo sapiens (human)
DOID:0080153
  • medium chain acyl-CoA dehydrogenase deficiency
Homo sapiens (human)
DOID:8337
  • appendicitis
  • Aliases:
    • acute appendicitis
    • acute appendicitis with generalized peritonitis
    • acute appendicitis with peritoneal abscess
Homo sapiens (human)
DOID:2280
  • hidradenitis suppurativa
  • Aliases:
    • Acne inversa, familial
Homo sapiens (human)
DOID:0050985
  • spinocerebellar ataxia type 38
Homo sapiens (human)
DOID:13096
  • Sneddon syndrome
  • Aliases:
    • Idiopathic livedo reticularis with systemic involvement
Homo sapiens (human)
DOID:4810
  • cerebrotendinous xanthomatosis
  • Aliases:
    • Cholestanol storage disease
Homo sapiens (human)
DOID:6740
  • cervix small cell carcinoma
  • Aliases:
    • small cell carcinoma of the Cervix Uteri
Homo sapiens (human)
DOID:0110722
  • neuronal ceroid lipofuscinosis 7
  • Aliases:
    • CLN7
Homo sapiens (human)
DOID:0110910
  • leukocyte adhesion deficiency 1
  • Aliases:
    • LAD1
    • LFA1 immunodeficiency
    • leukocyte adhesion deficiency type I
    • lymphocyte function-associated antigen 1 immunodeficiency
Homo sapiens (human)
DOID:4897
  • bile duct carcinoma
Homo sapiens (human)
DOID:0110240
  • cataract 20 multiple types
  • Aliases:
    • CTRCT20
Homo sapiens (human)
DOID:0050746
  • mantle cell lymphoma
Homo sapiens (human)
DOID:668
  • myositis ossificans
  • Aliases:
    • Myisitis ossificans
    • Ossification - muscle
Homo sapiens (human)
DOID:2211
  • factor XIII deficiency
  • Aliases:
    • Factor XIII deficiency disease
    • Hereditary factor XIII deficiency disease
    • deficiency, Laki-Lorand factor
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