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 3201 - 3225 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:893
  • Wilson disease
  • Aliases:
    • Cerebral pseudosclerosis
    • Westphal pseudosclerosis
    • Westphal-Strumpell syndrome
    • Wilson's disease
    • hepatolenticular degeneration
Homo sapiens (human)
DOID:0112223
  • developmental and epileptic encephalopathy 89
  • Aliases:
    • DEE89
    • early infantile epileptic encephalopathy 89
Homo sapiens (human)
DOID:557
  • kidney disease
  • Aliases:
    • impaired renal function disease
    • nephropathy
Homo sapiens (human)
DOID:10320
  • asbestosis
Homo sapiens (human)
DOID:0080158
  • herpes simplex virus keratitis
  • Aliases:
    • dendritic keratitis
Homo sapiens (human)
DOID:5379
  • hemoglobin E disease
  • Aliases:
    • Hb-E disease
Homo sapiens (human)
DOID:3827
  • congenital diaphragmatic hernia
  • Aliases:
    • Diaphragmatic Hernia
Homo sapiens (human)
DOID:0111387
  • familial isolated hypoparathyroidism
  • Aliases:
    • FIH
Homo sapiens (human)
DOID:0111027
  • hemochromatosis type 2A
  • Aliases:
    • HFE2A
Homo sapiens (human)
DOID:9544
  • refractory plasma cell neoplasm
Homo sapiens (human)
DOID:0090100
  • ocular albinism with sensorineural deafness
  • Aliases:
    • WS2-OA
    • autosomal recessive Waardenburg syndrome type 2 with ocular albinism
    • digenic Waardenburg syndrome/albinism
    • digenic Waardenburg syndrome/ocular albinism
Homo sapiens (human)
DOID:0060178
  • familial hemiplegic migraine
Homo sapiens (human)
DOID:4248
  • coronary stenosis
  • Aliases:
    • Coronary artery stenosis
Homo sapiens (human)
DOID:2800
  • acute interstitial pneumonia
  • Aliases:
    • AIP
    • Hamman-Rich disease
    • Hamman-Rich syndrome
    • Idiopathic pulmonary fibrosis, acute fatal form
    • accelerated interstitial pneumonia
    • acute interstitial pneumonitis
Homo sapiens (human)
DOID:4723
  • intracranial hypotension
Homo sapiens (human)
DOID:13207
  • proliferative diabetic retinopathy
  • Aliases:
    • PDR
Homo sapiens (human)
DOID:0060717
  • autosomal recessive congenital ichthyosis 8
  • Aliases:
    • ARCI8
    • lamellar ichthyosis 4
    • late-onset lamellar ichthyosis
Homo sapiens (human)
DOID:9498
  • pulmonary eosinophilia
Homo sapiens (human)
DOID:10071
  • larynx squamous papilloma
  • Aliases:
    • Laryngeal Squamous Cell Papilloma
Homo sapiens (human)
DOID:0080440
  • developmental and epileptic encephalopathy 3
  • Aliases:
    • early infantile epileptic encephalopathy 3
Homo sapiens (human)
DOID:11354
  • stone in bladder diverticulum
  • Aliases:
    • calculus in diverticulum of bladder
Homo sapiens (human)
DOID:4138
  • bile duct disease
  • Aliases:
    • bile duct disorder
    • disorder of bile duct
Homo sapiens (human)
DOID:0111444
  • progressive myoclonus epilepsy 4
  • Aliases:
    • AMRF
    • EPM4
    • Myoclonus-nephropathy syndrome
    • action myoclonus-renal failure syndrome
Homo sapiens (human)
DOID:1949
  • cholecystitis
  • Aliases:
    • acute and chronic cholecystitis
    • acute cholecystitis
    • acute on chronic cholecystitis
    • chronic cholecystitis
Homo sapiens (human)
DOID:0110565
  • autosomal dominant nonsyndromic deafness 3B
  • Aliases:
    • DFNA3B
    • autosomal dominant deafness 3B
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