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 1876 - 1900 of 7942 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism
DOID:9946
  • steroid-induced glaucoma
  • Aliases:
    • Corticosteroid-induced glaucoma
Homo sapiens (human)
DOID:403
  • mouth disease
Homo sapiens (human)
DOID:0111167
  • Dyggve-Melchior-Clausen disease
  • Aliases:
    • DMC disease
    • pseudo-Morquio disease type I
Homo sapiens (human)
DOID:4514
  • thyroid angiosarcoma
  • Aliases:
    • hemangiosarcoma of the Thyroid
Homo sapiens (human)
DOID:7519
  • endocervical carcinoma
  • Aliases:
    • carcinoma of endocervix
    • carcinoma of the Endocervix
Homo sapiens (human)
DOID:0080822
  • aspirin-induced respiratory disease
  • Aliases:
    • aspirin-sensitive asthma
Homo sapiens (human)
DOID:2384
  • Wernicke encephalopathy
  • Aliases:
    • Wernicke's disease
    • Wernicke's encephalopathy
Homo sapiens (human)
DOID:0111180
  • French Canadian Leigh disease
  • Aliases:
    • French Canadian type COX deficiency
    • French Canadian type Leigh syndrome
    • French Canadian type cytochrome c oxidase deficiency
    • Saguenay Lac saint Jean type COX deficiency
    • Saguenay Lac saint Jean type Leigh syndrome
    • mitochondrial complex IV deficiency nuclear type 5
Homo sapiens (human)
DOID:0050904
  • salivary gland carcinoma
Homo sapiens (human)
DOID:0111058
  • platelet-type bleeding disorder 12
  • Aliases:
    • BDPLT12
    • PGHS1 deficiency
    • platelet COX1 deficiency
    • platelet cyclooxygenase 1 deficiency
    • platelet prostaglandin-endoperoxide synthase 1 deficiency
Homo sapiens (human)
DOID:2825
  • nose disease
  • Aliases:
    • disorder of the nose
    • nasal disorder
Homo sapiens (human)
DOID:2965
  • bursitis
Homo sapiens (human)
DOID:14550
  • root resorption
Homo sapiens (human)
DOID:0111359
  • large congenital melanocytic nevus
  • Aliases:
    • Congenital pigmented nevus
    • GMN
    • Giant congenital melanocytic nevus
    • Giant pigmented hairy nevus
    • LCMN
Homo sapiens (human)
DOID:5830
  • cervical endometrioid adenocarcinoma
  • Aliases:
    • endometrioid carcinoma of the Cervix Uteri
Homo sapiens (human)
DOID:2938
  • Epstein-Barr virus infectious disease
  • Aliases:
    • EBV Infection
    • Epstein-Barr virus infection
Homo sapiens (human)
DOID:0080072
  • intestinal pseudo-obstruction
  • Aliases:
    • Chronic intestinal pseudo-obstruction
    • neuronal intestinal dysplasia
Homo sapiens (human)
DOID:7763
  • carcinoma of supraglottis
  • Aliases:
    • Supraglottic carcinoma
Homo sapiens (human)
DOID:7689
  • leptomeninges sarcoma
  • Aliases:
    • Leptomeningeal sarcoma
    • sarcoma of Leptomeninges
Homo sapiens (human)
DOID:10071
  • larynx squamous papilloma
  • Aliases:
    • Laryngeal Squamous Cell Papilloma
Homo sapiens (human)
DOID:3875
  • thrombophlebitis
  • Aliases:
    • Phlebitis and thrombophlebitis of superficial vessels of lower extremities
    • Superficial thrombophlebitis of leg
    • Thrombophlebitis of a superficial leg vein
    • Thrombophlebitis of superficial veins of lower extremity
Homo sapiens (human)
DOID:6496
  • obsolete extraskeletal myxoid chondrosarcoma
Homo sapiens (human)
DOID:0060867
  • macrocephaly-autism syndrome
  • Aliases:
    • macrocephaly-intellectual disability-autism syndrome
Homo sapiens (human)
DOID:3737
  • verrucous carcinoma
  • Aliases:
    • Warty carcinoma
    • verrucous squamous carcinoma
    • verrucous squamous cell carcinoma
Homo sapiens (human)
DOID:3279
  • spindle cell thymoma
  • Aliases:
    • Medullary Thymoma
    • Thymoma, medullary
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