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 14026 - 14050 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▼
DOID:0060652
  • familial erythrocytosis 1
  • Aliases:
    • ECYT1
    • autosomal dominant benign erythrocytosis
    • primary familial and congenital polycythemia
Mus musculus (house mouse)
DOID:0060652
  • familial erythrocytosis 1
  • Aliases:
    • ECYT1
    • autosomal dominant benign erythrocytosis
    • primary familial and congenital polycythemia
Xenopus laevis (African clawed frog)
DOID:0060651
  • MYH-9 related disease
Homo sapiens (human)
DOID:0060651
  • MYH-9 related disease
Mus musculus (house mouse)
DOID:0060650
  • dicarboxylic aminoaciduria
  • Aliases:
    • glutamate-aspartate transport defect
Mus musculus (house mouse)
DOID:0060650
  • dicarboxylic aminoaciduria
  • Aliases:
    • glutamate-aspartate transport defect
Caenorhabditis elegans
DOID:0060650
  • dicarboxylic aminoaciduria
  • Aliases:
    • glutamate-aspartate transport defect
Homo sapiens (human)
DOID:0060650
  • dicarboxylic aminoaciduria
  • Aliases:
    • glutamate-aspartate transport defect
Rattus norvegicus (Norway rat)
DOID:0060649
  • congenital hereditary endothelial dystrophy of cornea
  • Aliases:
    • CHED
Mus musculus (house mouse)
DOID:0060649
  • congenital hereditary endothelial dystrophy of cornea
  • Aliases:
    • CHED
Homo sapiens (human)
DOID:0060648
  • anterior segment dysgenesis
  • Aliases:
    • anterior segment developmental anomaly
    • corneal opacification and other ocular anomalies
    • sclerocornea with other ocular anomalies
Mus musculus (house mouse)
DOID:0060648
  • anterior segment dysgenesis
  • Aliases:
    • anterior segment developmental anomaly
    • corneal opacification and other ocular anomalies
    • sclerocornea with other ocular anomalies
Homo sapiens (human)
DOID:0060647
  • fetal encasement syndrome
  • Aliases:
    • cocoon syndrome
Homo sapiens (human)
DOID:0060646
  • congenital chylothorax
Mus musculus (house mouse)
DOID:0060646
  • congenital chylothorax
Homo sapiens (human)
DOID:0060646
  • congenital chylothorax
Drosophila melanogaster (fruit fly)
DOID:0060645
  • chronic recurrent multifocal osteomyelitis
  • Aliases:
    • CRMO
    • chronic multifocal osteomyelitis
Homo sapiens (human)
DOID:0060645
  • chronic recurrent multifocal osteomyelitis
  • Aliases:
    • CRMO
    • chronic multifocal osteomyelitis
Rattus norvegicus (Norway rat)
DOID:0060645
  • chronic recurrent multifocal osteomyelitis
  • Aliases:
    • CRMO
    • chronic multifocal osteomyelitis
Mus musculus (house mouse)
DOID:0060644
  • chondrodysplasia-pseudohermaphroditism syndrome
  • Aliases:
    • Nivelon-Nivelon-Mabille syndrome
    • chondrodysplasia-disorder of sex development syndrome
Saccharomyces cerevisiae S288C
DOID:0060643
  • primary sclerosing cholangitis
Mus musculus (house mouse)
DOID:0060643
  • primary sclerosing cholangitis
Saccharomyces cerevisiae S288C
DOID:0060643
  • primary sclerosing cholangitis
Drosophila melanogaster (fruit fly)
DOID:0060643
  • primary sclerosing cholangitis
Homo sapiens (human)
DOID:0060643
  • primary sclerosing cholangitis
Danio rerio (zebrafish)

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