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 1901 - 1925 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼
DOID:5675
  • cribriform carcinoma
  • Aliases:
    • ductal carcinoma, cribriform type
Homo sapiens (human)
DOID:0110011
  • advanced sleep phase syndrome 1
  • Aliases:
    • FASPS1
    • familial advanced sleep phase syndrome 1
Homo sapiens (human)
DOID:0110757
  • type 1 diabetes mellitus 20
  • Aliases:
    • IDDM20
    • Insulin-Dependent Diabetes Mellitus 20
Homo sapiens (human)
DOID:4473
  • sarcomatoid renal cell carcinoma
  • Aliases:
    • renal cell carcinoma, spindle cell
Homo sapiens (human)
DOID:4376
  • milk allergy
  • Aliases:
    • milk allergic reaction
Homo sapiens (human)
DOID:9428
  • intracranial hypertension
  • Aliases:
    • Raised intracranial pressure
Homo sapiens (human)
DOID:14735
  • hereditary angioedema
  • Aliases:
    • HANE
    • Hereditary angioneurotic edema
Homo sapiens (human)
DOID:0110748
  • obsolete type 1 diabetes mellitus 9
  • Aliases:
    • IDDM9
    • Insulin-Dependent Diabetes Mellitus 9
Homo sapiens (human)
DOID:0050120
  • hemophagocytic lymphohistiocytosis
  • Aliases:
    • haemophagocytic syndrome
Homo sapiens (human)
DOID:6652
  • diffuse idiopathic skeletal hyperostosis
  • Aliases:
    • Ankylosing vertebral hyperostosis
    • DISH
    • Disseminated idiopathic skeletal hyperostosis
Homo sapiens (human)
DOID:0110741
  • type 1 diabetes mellitus 2
  • Aliases:
    • IDDM2
    • Insulin-Dependent Diabetes Mellitus 2
Homo sapiens (human)
DOID:12577
  • urethral obstruction
  • Aliases:
    • Obstruction of urethra
Homo sapiens (human)
DOID:0080569
  • congenital disorder of glycosylation Ir
  • Aliases:
    • congenital disorder of glycosylation 1r
Homo sapiens (human)
DOID:10324
  • anthracosilicosis
Homo sapiens (human)
DOID:13098
  • central retinal artery occlusion
Homo sapiens (human)
DOID:0110444
  • dilated cardiomyopathy 1X
  • Aliases:
    • CMD1X
    • dilated cardiomyopathy with mild or no proximal muscle weakness
Homo sapiens (human)
DOID:0050719
  • cerebral folate receptor alpha deficiency
  • Aliases:
    • Neurodegeneration due to cerebral folate transport deficiency
Homo sapiens (human)
DOID:0081381
  • juvenile amyotrophic lateral sclerosis type 27
Homo sapiens (human)
DOID:10159
  • osteonecrosis
  • Aliases:
    • Avascular necrosis of bone
    • aseptic necrosis
    • bone necrosis
Homo sapiens (human)
DOID:3405
  • histiocytosis
  • Aliases:
    • Hand Schuller Christian disease
    • chronic Histiocytosis X
Homo sapiens (human)
DOID:6271
  • gastric cardia adenocarcinoma
  • Aliases:
    • adenocarcinoma of Cardia of stomach
Homo sapiens (human)
DOID:0090084
  • hypogonadotropic hypogonadism 5 with or without anosmia
Homo sapiens (human)
DOID:12003
  • trachea squamous cell carcinoma
  • Aliases:
    • Tracheal Epidermoid carcinoma
Homo sapiens (human)
DOID:10881
  • hand, foot and mouth disease
  • Aliases:
    • Vesicular stomatitis and exanthem
Homo sapiens (human)
DOID:1811
  • reflex sympathetic dystrophy
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