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 1 - 10 of 51 in total
Gene ID Gene Symbol Description Source
43 ACHE acetylcholinesterase (Yt blood group)
248 ALPI alkaline phosphatase, intestinal
250 ALPP alkaline phosphatase, placental
275 AMT aminomethyltransferase
412 STS steroid sulfatase
847 CAT catalase
945 CD33 CD33 molecule
1113 CHGA chromogranin A
1116 CHI3L1 chitinase 3 like 1
1118 CHIT1 chitinase 1
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 21 - 30 of 58 in total
HPO ID HPO Term
HP:0002067 Bradykinesia
HP:0002072 Chorea
HP:0002073 Progressive cerebellar ataxia
HP:0002283 Global brain atrophy
HP:0002312 Clumsiness
HP:0002401 Stroke-like episode
HP:0002446 Astrocytosis
HP:0002464 Spastic dysarthria
HP:0002529 Neuronal loss in central nervous system
HP:0002922 Increased CSF protein concentration
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