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 451 - 475 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:12169
  • carpal tunnel syndrome
  • Aliases:
    • CTS - Carpal tunnel syndrome
    • Median nerve entrapment
    • carpal tunnel median neuropathy
Homo sapiens (human)
DOID:2228
  • thrombocytosis
  • Aliases:
    • Thrombocythaemia
Homo sapiens (human)
DOID:7960
  • malignant spiradenoma
  • Aliases:
    • malignant eccrine spiradenoma
Homo sapiens (human)
DOID:5386
  • lung adenoma
  • Aliases:
    • adenoma of lung
    • pulmonary adenoma
Homo sapiens (human)
DOID:4451
  • renal carcinoma
  • Aliases:
    • carcinoma of kidney
    • kidney carcinoma
Homo sapiens (human)
DOID:5292
  • mediastinum leiomyosarcoma
  • Aliases:
    • leiomyosarcoma of mediastinum
Homo sapiens (human)
DOID:1703
  • Richter's syndrome
  • Aliases:
    • Richter syndrome
Homo sapiens (human)
DOID:12642
  • hiatus hernia
  • Aliases:
    • Diaphragmatic - hiatus -hernia
    • hiatal hernia
Homo sapiens (human)
DOID:13628
  • favism
Homo sapiens (human)
DOID:3512
  • neurofibrosarcoma
  • Aliases:
    • Neurosarcoma
Homo sapiens (human)
DOID:0111265
  • Boucher-Neuhauser syndrome
  • Aliases:
    • ataxia-hypogonadism-choroidal dystrophy syndrome
Homo sapiens (human)
DOID:8717
  • decubitus ulcer
  • Aliases:
    • Decubitus (pressure) ulcer
    • Decubitus ulcer any site
    • pressure sores
    • pressure ulcer
Homo sapiens (human)
DOID:349
  • systemic mastocytosis
  • Aliases:
    • SMCD - systemic mast cell disease
    • systemic tissue mast cell disease
Homo sapiens (human)
DOID:0050589
  • inflammatory bowel disease
Homo sapiens (human)
DOID:11665
  • Patau syndrome
  • Aliases:
    • D1 Trisomy
    • trisomy 13
Homo sapiens (human)
DOID:13777
  • epidermodysplasia verruciformis
Homo sapiens (human)
DOID:0060849
  • osteoporosis-pseudoglioma syndrome
  • Aliases:
    • OPPG
    • ocular form of osteogenesis imperfecta
Homo sapiens (human)
DOID:11189
  • pulp degeneration
Homo sapiens (human)
DOID:681
  • progressive bulbar palsy
Homo sapiens (human)
DOID:0080433
  • developmental and epileptic encephalopathy 51
  • Aliases:
    • DEE51
    • early infantile epileptic encephalopathy 51
Homo sapiens (human)
DOID:12450
  • pancytopenia
Homo sapiens (human)
DOID:10024
  • migraine with aura
  • Aliases:
    • classic migraine
Homo sapiens (human)
DOID:2710
  • sick building syndrome
Homo sapiens (human)
DOID:0070258
  • congenital disorder of glycosylation type IIf
  • Aliases:
    • CDG IIf
    • CDG2F
    • CDGIIdf
    • CMP-sialic acid transporter deficiency
    • Carbohydrate deficient glycoprotein syndrome type IIf
    • SLC35A1-CDG
Homo sapiens (human)
DOID:2526
  • prostate adenocarcinoma
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