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 4326 - 4350 of 4649 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼ Source
DOID:0111102
  • maturity-onset diabetes of the young type 3
  • Aliases:
    • MODY type 3
    • MODY3
Homo sapiens (human)
DOID:0050451
  • Brugada syndrome
  • Aliases:
    • Bangungut
    • Brugada type idiopathic ventricular fibrillation
    • Dream disease
    • Pokkuri death syndrome
    • SUNDS
    • sudden unexplained nocturnal death syndrome
Homo sapiens (human)
DOID:0060546
  • Hermansky-Pudlak syndrome 8
Homo sapiens (human)
DOID:0111105
  • maturity-onset diabetes of the young type 8
  • Aliases:
    • MODY type 8
    • MODY8
    • diabetes and pancreatic exocrine
    • maturity-onset diabetes of the young type 8 with exocrine dysfunction
Homo sapiens (human)
DOID:962
  • neurofibroma
Homo sapiens (human)
DOID:6271
  • gastric cardia adenocarcinoma
  • Aliases:
    • adenocarcinoma of Cardia of stomach
Homo sapiens (human)
DOID:0080716
  • infantile liver failure syndrome
Homo sapiens (human)
DOID:0111800
  • syndromic microphthalmia 12
  • Aliases:
    • MCOPS12
    • microphthalmia with or without pulmonary hypoplasia, diaphragmatic hernia, and/or cardiac defects
Homo sapiens (human)
DOID:2352
  • hemochromatosis
  • Aliases:
    • Haemochromatosis
    • diabetes bronze
    • iron storage disorder
Homo sapiens (human)
DOID:2975
  • cystic kidney disease
  • Aliases:
    • renal Cyst
Homo sapiens (human)
DOID:0070399
  • hypomyelinating leukodystrophy 18
  • Aliases:
    • HLD18
Homo sapiens (human)
DOID:0090050
  • dystonia 27
Homo sapiens (human)
DOID:1875
  • impotence
  • Aliases:
    • Sexual impotence
    • erectile dysfunction
Homo sapiens (human)
DOID:0070004
  • myeloid neoplasm
Homo sapiens (human)
DOID:50
  • thyroid gland disease
Homo sapiens (human)
DOID:3774
  • chordoid glioma
  • Aliases:
    • Chordoid glioma of 3rd Ventricle
    • Chordoid glioma of third ventricle
    • third ventricle chordoid glioma
Homo sapiens (human)
DOID:0081395
  • Harel-Yoon syndrome
  • Aliases:
    • Ocular anomalies-axonal neuropathy-developmental delay syndrome
Homo sapiens (human)
DOID:2562
  • suppurative periapical periodontitis
  • Aliases:
    • Apical abscess
    • Dentoalveolar abscess
    • Periapical abscess
    • Suppurative apical periodontitis
Homo sapiens (human)
DOID:0080076
  • Neu-Laxova syndrome 1
Homo sapiens (human)
DOID:0080153
  • medium chain acyl-CoA dehydrogenase deficiency
Homo sapiens (human)
DOID:620
  • blood protein disease
  • Aliases:
    • blood protein disorder
Homo sapiens (human)
DOID:0050590
  • severe congenital neutropenia
Homo sapiens (human)
DOID:0060576
  • 3MC syndrome 2
Homo sapiens (human)
DOID:1495
  • cystic echinococcosis
  • Aliases:
    • Echinococcus granulosus infection
    • Echinococcus granulosus infection of lung
    • Echinococcus granulosus infection of thyroid
    • Liver echinococcus granulosus
    • Thyroid echinococcus granulosus
    • echinococcus granulosus
    • echinococcus granulosus infectious disease
    • echinococcus granulosus infectious disease of liver
    • echinococcus granulosus infectious disease of thyroid
    • lung echinococcus granulosus
    • unilocular echinococcosis
    • unilocular hydatid disease
Homo sapiens (human)
DOID:1701
  • steroid inherited metabolic disorder
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: February 17, 2025