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 201 - 225 of 4649 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▼
DOID:9410
  • panhypopituitarism
  • Aliases:
    • Simmond's disease
    • Simmonds' disease
    • combined pituitary hormone deficiency
Homo sapiens (human)
DOID:9409
  • diabetes insipidus
Homo sapiens (human)
DOID:9408
  • acute myocardial infarction
Homo sapiens (human)
DOID:9406
  • hypopituitarism
  • Aliases:
    • Pituitary insufficiency
    • pituitary hormone deficiency
Homo sapiens (human)
DOID:9402
  • epididymitis
Homo sapiens (human)
DOID:9383
  • iridocyclitis
  • Aliases:
    • primary iridocyclitis
Homo sapiens (human)
DOID:9368
  • keratoconjunctivitis
Homo sapiens (human)
DOID:9362
  • status asthmaticus
  • Aliases:
    • Asthma with status asthmaticus
    • Severe asthma attack
Homo sapiens (human)
DOID:936
  • brain disease
  • Aliases:
    • encephalopathy
Homo sapiens (human)
DOID:9352
  • type 2 diabetes mellitus
  • Aliases:
    • NIDDM
    • insulin resistance
    • non-insulin-dependent diabetes mellitus
    • type 2 diabetes
    • type II diabetes mellitus
Homo sapiens (human)
DOID:9351
  • diabetes mellitus
  • Aliases:
    • diabetes
Homo sapiens (human)
DOID:934
  • viral infectious disease
  • Aliases:
    • Viral Infection
    • Viral disease
    • virus infection
Homo sapiens (human)
DOID:93
  • language disorder
Homo sapiens (human)
DOID:9296
  • cleft lip
  • Aliases:
    • Labium leporinum
    • cheiloschisis
    • cleft lip, unilateral, complete
    • complete unilateral cleft lip
    • hare lip
Homo sapiens (human)
DOID:9286
  • priapism
  • Aliases:
    • Mentulagra
Homo sapiens (human)
DOID:9282
  • ocular hypertension
Homo sapiens (human)
DOID:9281
  • phenylketonuria
  • Aliases:
    • Folling's disease
    • PKU
    • maternal phenylketonuria
    • phenylalaninemia
Homo sapiens (human)
DOID:9280
  • carbamoyl phosphate synthetase I deficiency disease
  • Aliases:
    • CPS I deficiency
Homo sapiens (human)
DOID:9279
  • hyperhomocysteinemia
Homo sapiens (human)
DOID:9277
  • primary cerebellar degeneration
Homo sapiens (human)
DOID:9273
  • citrullinemia
  • Aliases:
    • ASS deficiency
    • deficiency of citrulline-aspartate ligase
Homo sapiens (human)
DOID:9271
  • ornithine carbamoyltransferase deficiency
  • Aliases:
    • deficiency of citrulline phosphorylase
    • ornithine transcarbamylase deficiency
Homo sapiens (human)
DOID:9270
  • alkaptonuria
  • Aliases:
    • Homogentisate 1,2-dioxygenase deficiency
    • alcaptonuria
Homo sapiens (human)
DOID:9269
  • maple syrup urine disease
  • Aliases:
    • Ketoacidaemia
    • branched chain ketoaciduria
Homo sapiens (human)
DOID:9268
  • glycine encephalopathy
  • Aliases:
    • Non-ketotic hyperglycinemia
    • nonketotic hyperglycinemia
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 v4.0.0

Last updated: August 19, 2024