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 926 - 950 of 4649 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▼
DOID:2876
  • laryngeal squamous cell carcinoma
  • Aliases:
    • Epidermoid carcinoma of the Larynx
    • squamous cell carcinoma of larynx
Homo sapiens (human)
DOID:2871
  • endometrial carcinoma
  • Aliases:
    • carcinoma of the Endometrium
    • endometrioid carcinoma
    • endometrioid carcinoma of female Reproductive system
Homo sapiens (human)
DOID:2870
  • endometrial adenocarcinoma
  • Aliases:
    • adenocarcinoma of endometrium
    • adenocarcinoma of the Endometrium
    • adenocarcinoma of uterus
    • endometrial adenoacanthoma
    • endometrial endometrioid adenocarcinoma
    • endometrial endometrioid adenocarcinoma with squamous differentiation
    • endometrioid adenoma or carcinoma
    • endometrioid adenomas and carcinomas
    • endometrioid carcinoma of Endometrium
Homo sapiens (human)
DOID:2862
  • glucosephosphate dehydrogenase deficiency
  • Aliases:
    • Glucose-6-phosphate dehydrogenase deficiency
    • deficiency of G-6PD
Homo sapiens (human)
DOID:2861
  • congenital nonspherocytic hemolytic anemia
  • Aliases:
    • HNSHA
    • congenital nonspherocytic hemolytic anaemia
    • hereditary nonspherocytic hemolytic anaemia
    • hereditary nonspherocytic hemolytic anemia
Homo sapiens (human)
DOID:2860
  • hemoglobinopathy
  • Aliases:
    • hemoglobinopathies
Homo sapiens (human)
DOID:2859
  • hemoglobin C disease
  • Aliases:
    • Hb-C disease
Homo sapiens (human)
DOID:2855
  • hyperthyroxinemia
Homo sapiens (human)
DOID:285
  • hairy cell leukemia
Homo sapiens (human)
DOID:2843
  • long QT syndrome
  • Aliases:
    • LQT
    • long Q-T syndrome
Homo sapiens (human)
DOID:2842
  • Jervell-Lange Nielsen syndrome
  • Aliases:
    • Jervell and Lange-Nielson syndrome
Homo sapiens (human)
DOID:2841
  • asthma
  • Aliases:
    • bronchial hyperreactivity
    • chronic obstructive asthma
    • chronic obstructive asthma with acute exacerbation
    • chronic obstructive asthma with status asthmaticus
Homo sapiens (human)
DOID:2835
  • polycythemia due to hypoxia
Homo sapiens (human)
DOID:2810
  • middle lobe syndrome
Homo sapiens (human)
DOID:28
  • endocrine system disease
Homo sapiens (human)
DOID:2799
  • bronchiolitis obliterans
  • Aliases:
    • Bronchiolitis exudativa
    • Bronchiolitis fibrosa obliterans
    • Obliterative bronchiolitis
Homo sapiens (human)
DOID:2797
  • idiopathic interstitial pneumonia
  • Aliases:
    • Diffuse idiopathic pulmonary fibrosis
    • Idiopathic fibrosing alveolitis
Homo sapiens (human)
DOID:2786
  • cerebellar disease
Homo sapiens (human)
DOID:2785
  • Dandy-Walker syndrome
  • Aliases:
    • Atresia of foramina of Magendie and Luschka
Homo sapiens (human)
DOID:2773
  • contact dermatitis
  • Aliases:
    • Contact dermatitis/eczema
    • Contact eczema
    • Dermatitis, venenata
    • dermatitis venenata
Homo sapiens (human)
DOID:2772
  • irritant dermatitis
  • Aliases:
    • irritant contact dermatitis
    • primary irritant dermatitis
Homo sapiens (human)
DOID:2755
  • Mycobacterium avium complex disease
  • Aliases:
    • Infection due to Mycobacterium intracellulare
    • MAC disease
    • Mycobacterium Avium Infection
    • Mycobacterium avium Complex
Homo sapiens (human)
DOID:2754
  • glycogen storage disease VI
  • Aliases:
    • Glycogen storage disease 6
    • Hers' disease
    • glycogen storage disease type VI
    • hepatic glycogen phosphorylase deficiency
    • hepatophosphorylase deficiency glycogenosis
Homo sapiens (human)
DOID:2750
  • glycogen storage disease IV
  • Aliases:
    • Amylopectinosis
    • Branching-transferase deficiency glycogenosis
    • Glycogen storage disease 4
    • Glycogen storage disease, type IV
    • brancher deficiency glycogenosis
    • deficiency of 1,4-alpha-glucan branching enzyme
Homo sapiens (human)
DOID:2749
  • glycogen storage disease Ia
Homo sapiens (human)

About Release Notes Help Feedback

International Collaboration

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.1.0

Last updated: December 9, 2024