Creutzfeldt-Jakob disease

Summary
Synonym
  • CJD
  • Creutzfeldt Jacob syndrome
  • Creutzfeldt Jakob disease
  • Creutzfeldt-Jacob disease
  • Jakob-Creutzfeldt disease
  • Subacute spongiform encephalopathy
  • Transmissible virus dementia
Super Class
prion disease
External Links
Disease Ontology
DOID:11949
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying entries 11 - 20 of 51 in total
Gene ID Gene Symbol Description Source
1636 ACE angiotensin I converting enzyme
1718 DHCR24 24-dehydrocholesterol reductase
2023 ENO1 enolase 1
2026 ENO2 enolase 2
2220 FCN2 ficolin 2
2539 G6PD glucose-6-phosphate dehydrogenase
2581 GALC galactosylceramidase
2821 GPI glucose-6-phosphate isomerase
3251 HPRT1 hypoxanthine phosphoribosyltransferase 1
3425 IDUA alpha-L-iduronidase
Displaying 1 entry
Gene ID Gene Symbol Description Source
14420 Galc galactosylceramidase
Displaying 1 entry
Gene ID Gene Symbol Description Source
449649 galca galactosylceramidase a
Displaying all 2 entries
Gene ID Gene Symbol Description Source Organism
446948 galc.L galactosylceramidase L homeolog Xenopus laevis (African clawed frog)
779723 galc galactosylceramidase Xenopus tropicalis (tropical clawed frog)
Displaying 1 entry
Gene ID Gene Symbol Description Source
183002 C29E4.10 Putative galactocerebrosidase
The Human Phenotype Ontology
Displaying entries 1 - 10 of 58 in total
HPO ID HPO Term
HP:0000504 Abnormality of vision
HP:0000605 Supranuclear gaze palsy
HP:0000639 Nystagmus
HP:0000712 Emotional lability
HP:0000716 Depression
HP:0000726 Dementia
HP:0000736 Short attention span
HP:0000737 Irritability
HP:0000738 Hallucinations
HP:0000739 Anxiety
Displaying 1 entry
Gene ID Gene Symbol Description
5621 PRNP prion protein (Kanno blood group)

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024