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 October 9, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 276 - 300 of 15957 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism Source
DOID:576
  • proteinuria
Homo sapiens (human)
DOID:7147
  • ankylosing spondylitis
  • Aliases:
    • Bekhterev syndrome
    • Bekhterev's disease
    • Marie-Strumpell disease
Homo sapiens (human)
DOID:1591
  • renovascular hypertension
Homo sapiens (human)
DOID:2921
  • glomerulonephritis
Homo sapiens (human)
DOID:7693
  • abdominal aortic aneurysm
  • Aliases:
    • AORTIC ANEURYSM, FAMILIAL ABDOMINAL 1
Homo sapiens (human)
DOID:3021
  • acute kidney failure
Homo sapiens (human)
DOID:820
  • myocarditis
  • Aliases:
    • Myocardial inflammation
Homo sapiens (human)
DOID:0060224
  • atrial fibrillation
  • Aliases:
    • A-fib
    • AFib
Homo sapiens (human)
DOID:3770
  • pulmonary fibrosis
  • Aliases:
    • Fibrosis of lung
Homo sapiens (human)
DOID:5419
  • schizophrenia
  • Aliases:
    • schizophrenia-1
Homo sapiens (human)
DOID:11476
  • osteoporosis
Homo sapiens (human)
DOID:8805
  • intermediate coronary syndrome
  • Aliases:
    • Angina at rest
    • Anginal chest pain at rest
    • Impending infarction
    • Preinfarction angina
    • Unstable angina
    • Worsening angina
Homo sapiens (human)
DOID:1205
  • allergic disease
  • Aliases:
    • allergic hypersensitivity disease
    • hypersensitivity
    • hypersensitivity reaction type I disease
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)
DOID:988
  • mitral valve prolapse
  • Aliases:
    • Barlow's syndrome
    • floppy mitral valve
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:0050851
  • glomerulosclerosis
Homo sapiens (human)
DOID:11335
  • sarcoidosis
  • Aliases:
    • Boeck sarcoid
    • lymphogranulomatosis
Homo sapiens (human)
DOID:10952
  • nephritis
Homo sapiens (human)
DOID:3827
  • congenital diaphragmatic hernia
  • Aliases:
    • Diaphragmatic Hernia
Homo sapiens (human)
DOID:0110861
  • autosomal recessive polycystic kidney disease
  • Aliases:
    • Arpkd
    • Pkhd1
    • Polycystic Kidney Disease, Infantile, Type I
    • Polycystic Kidney and Hepatic Disease 1
Homo sapiens (human)
DOID:11400
  • pyelonephritis
Homo sapiens (human)
DOID:2527
  • nephrosis
Homo sapiens (human)
DOID:2355
  • anemia
  • Aliases:
    • anaemia
Homo sapiens (human)
DOID:13141
  • uveitis
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: December 9, 2024