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 13076 - 13100 of 15957 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism Source
DOID:8778
  • Crohn's disease
  • Aliases:
    • Crohn disease
    • Crohn's disease of colon
    • Crohn's disease of large bowel
    • Granulomatous Colitis
    • Pediatric Crohn's disease
Rattus norvegicus (Norway rat)
DOID:0111630
  • familial erythrocytosis 8
  • Aliases:
    • BPGM deficiency
    • DPGM deficiency
    • ECYT8
    • bisphosphoglycerate mutase deficiency
    • bisphosphoglyceromutase deficiency
    • diphosphoglycerate mutase deficiency of erythrocyte
    • hemolytic anemia due to diphosphoglycerate mutase deficiency
Mus musculus (house mouse)
DOID:8677
  • perinatal necrotizing enterocolitis
  • Aliases:
    • ENTEROCOLITIS NECROTIZING
    • Necrotizing enterocolitis in fetus OR newborn
    • Perinatal necrotising enterocolitis
    • Pseudomembranous enterocolitis in newborn
    • necrotizing enterocolitis
Mus musculus (house mouse)
DOID:14250
  • Down syndrome
  • Aliases:
    • Complete trisomy 21 syndrome
    • Down's syndrome
    • Down's syndrome - trisomy 21
    • Downs syndrome
    • G Trisomy
    • trisomy 21 syndrome
Mus musculus (house mouse)
DOID:0081268
  • pulmonary venoocclusive disease 1
Mus musculus (house mouse)
DOID:1681
  • heart septal defect
  • Aliases:
    • Cardiac septal defects
    • Congenital septal defect of heart
    • septal defect
Mus musculus (house mouse)
DOID:0060389
  • chromosome 10q23 deletion syndrome
Rattus norvegicus (Norway rat)
DOID:0111686
  • hereditary mixed polyposis syndrome 2
  • Aliases:
    • HMPS2
Rattus norvegicus (Norway rat)
DOID:14289
  • Ebstein anomaly
  • Aliases:
    • Ebstein's anomaly
    • Ebstein's anomaly of common atrioventricular valve
    • Ebstein's anomaly of right atrioventricular valve
    • Ebstein's anomaly of tricuspid valve
Rattus norvegicus (Norway rat)
DOID:5295
  • intestinal disease
Rattus norvegicus (Norway rat)
DOID:384
  • Wolff-Parkinson-White syndrome
  • Aliases:
    • Anomalous A-V excitation
    • Wolff-Parkinson-White pattern
    • anomalous atrioventricular excitation
Rattus norvegicus (Norway rat)
DOID:0060389
  • chromosome 10q23 deletion syndrome
Mus musculus (house mouse)
DOID:14289
  • Ebstein anomaly
  • Aliases:
    • Ebstein's anomaly
    • Ebstein's anomaly of common atrioventricular valve
    • Ebstein's anomaly of right atrioventricular valve
    • Ebstein's anomaly of tricuspid valve
Mus musculus (house mouse)
DOID:0111686
  • hereditary mixed polyposis syndrome 2
  • Aliases:
    • HMPS2
Mus musculus (house mouse)
DOID:384
  • Wolff-Parkinson-White syndrome
  • Aliases:
    • Anomalous A-V excitation
    • Wolff-Parkinson-White pattern
    • anomalous atrioventricular excitation
Mus musculus (house mouse)
DOID:12556
  • acute kidney tubular necrosis
  • Aliases:
    • ATN - acute tubular necrosis
    • acute renal Failure with tubular necrosis
    • acute renal failure with lesion of tubular necrosis
    • acute tubular necrosis
    • acute tubule necrosis
Mus musculus (house mouse)
DOID:0060306
  • Meier-Gorlin syndrome
  • Aliases:
    • ear-patella-short stature syndrome
Mus musculus (house mouse)
DOID:0080404
  • orofacial cleft 11
  • Aliases:
    • nonsyndromic cleft lip with or without cleft palate 11
Mus musculus (house mouse)
DOID:0110122
  • Axenfeld-Rieger syndrome type 3
  • Aliases:
    • Axenfeld-Rieger anomaly with or without cardiac defects and/or sensorineural hearing loss
    • RIEG3
    • Rieger syndrome type 3
    • anterior chamber cleavage syndrome
    • anterior segment mesenchymal dysgenesis
Mus musculus (house mouse)
DOID:0111805
  • syndromic microphthalmia 6
  • Aliases:
    • Bakrania-Ragge syndrome
    • MCOPS6
    • anophthalmia clinical with micrognathia malformed ears digital anomalies and abnormal external genitalia
    • microphthalmia and pituitary anomalies
    • microphthalmia with brain and digit anomalies
    • syndromic microphthalmia type 6
Mus musculus (house mouse)
DOID:540
  • strabismus
Mus musculus (house mouse)
DOID:1222
  • cartilage disease
  • Aliases:
    • Cartilage disorder
    • Chondropathy
Mus musculus (house mouse)
DOID:0080015
  • physical disorder
  • Aliases:
    • congenital disorder
Mus musculus (house mouse)
DOID:668
  • myositis ossificans
  • Aliases:
    • Myisitis ossificans
    • Ossification - muscle
Mus musculus (house mouse)
DOID:18
  • urinary system disease
  • Aliases:
    • Non-neoplastic urinary tract disease
    • urinary tract disease
Mus musculus (house mouse)

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