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
Disease Ontology
DOID:11949
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
GARD
MGI genotype (from TogoID)
Related Genes
Displaying all 3 entries
Gene ID Gene Symbol Description Source
3119 HLA-DQB1 major histocompatibility complex, class II, DQ beta 1
5621 PRNP prion protein (Kanno blood group)
6804 STX1A syntaxin 1A
Displaying 1 entry
Gene ID Gene Symbol Description Source
19122 Prnp prion protein
Related Glycoprotein
The Human Phenotype Ontology
Displaying entries 41 - 50 of 58 in total
HPO ID HPO Term
HP:0010846 EEG with persistent abnormal rhythmic activity
HP:0011099 Spastic hemiparesis
HP:0012332 Abnormal autonomic nervous system physiology
HP:0012672 Akinetic mutism
HP:0100256 Senile plaques
HP:0100292 Amyloidosis of peripheral nerves
HP:0100661 Trigeminal neuralgia
HP:0100785 Insomnia
HP:0100786 Hypersomnia
HP:0000006 Autosomal dominant inheritance
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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