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 101 - 125 of 4649 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism Source
DOID:0080199
  • colorectal carcinoma
Homo sapiens (human)
DOID:850
  • lung disease
Homo sapiens (human)
DOID:1289
  • neurodegenerative disease
  • Aliases:
    • degenerative disease
Homo sapiens (human)
DOID:3587
  • pancreatic ductal carcinoma
  • Aliases:
    • malignant neoplasm of duct of Wirsung
    • pancreatic duct cancer
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:9498
  • pulmonary eosinophilia
Homo sapiens (human)
DOID:0050679
  • blue cone monochromacy
Homo sapiens (human)
DOID:1612
  • breast cancer
  • Aliases:
    • breast tumor
    • malignant neoplasm of breast
    • malignant tumor of the breast
    • mammary cancer
    • mammary tumor
    • primary breast cancer
Homo sapiens (human)
DOID:2671
  • transitional cell carcinoma
  • Aliases:
    • transitional carcinoma
    • transitional cell tumor
    • urothelial cell carcinoma
Homo sapiens (human)
DOID:3008
  • invasive ductal carcinoma
  • Aliases:
    • Infiltrating ductal carcinoma of breast
    • Invasive ductal carcinoma, NST
    • ductal adenocarcinoma
Homo sapiens (human)
DOID:0110052
  • amelogenesis imperfecta type 1B
  • Aliases:
    • AI1B
    • AIH2
    • amelogenesis imperfecta type IB
    • autosomal dominant hypoplastic local amelogenesis imperfecta
    • hereditary localized enamel hypoplasia
Homo sapiens (human)
DOID:0110056
  • amelogenesis imperfecta type 1C
  • Aliases:
    • AI1C
    • amelogenesis imperfecta type IC
    • autosomal recessive amelogenesis imperfecta hypoplastic with or without openbite malocclusion
    • autosomal recessive amelogenesis imperfecta local hypoplastic type
Homo sapiens (human)
DOID:2394
  • ovarian cancer
  • Aliases:
    • malignant Ovarian tumor
    • malignant tumour of ovary
    • ovarian neoplasm
    • ovary neoplasm
    • primary ovarian cancer
    • tumor of the Ovary
Homo sapiens (human)
DOID:4362
  • cervical cancer
  • Aliases:
    • cervical neoplasm
    • cervix cancer
    • cervix uteri cancer
    • neoplasm of uterine cervix
    • tumor of the Cervix Uteri
    • uterine cervical neoplasm
Homo sapiens (human)
DOID:11054
  • urinary bladder cancer
  • Aliases:
    • bladder cancer
    • tumor of the bladder
Homo sapiens (human)
DOID:3459
  • breast carcinoma
  • Aliases:
    • Mammary carcinoma
    • carcinoma of breast
Homo sapiens (human)
DOID:2349
  • arteriosclerosis
  • Aliases:
    • Arteriosclerotic vascular disease
Homo sapiens (human)
DOID:303
  • substance-related disorder
Homo sapiens (human)
DOID:2871
  • endometrial carcinoma
  • Aliases:
    • carcinoma of the Endometrium
    • endometrioid carcinoma
    • endometrioid carcinoma of female Reproductive system
Homo sapiens (human)
DOID:4247
  • coronary restenosis
Homo sapiens (human)
DOID:14250
  • Down syndrome
  • Aliases:
    • Complete trisomy 21 syndrome
    • Down's syndrome
    • Down's syndrome - trisomy 21
    • Downs syndrome
    • G Trisomy
    • trisomy 21 syndrome
Homo sapiens (human)
DOID:3652
  • Leigh disease
  • Aliases:
    • Infantile necrotizing encephalomyelopathy
    • Leigh syndrome
    • juvenile subacute necrotizing encephalomyelopathy
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:0050888
  • syndromic intellectual disability
Homo sapiens (human)
DOID:0070033
  • autosomal dominant intellectual developmental disorder 3
  • Aliases:
    • MRD3
    • autosomal dominant mental retardation 3
    • autosomal dominant non-syndromic intellectual disability 3
Homo sapiens (human)

About Release Notes Help Feedback

Click here to visit the beta site.


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