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 21 - 30 of 51 in total
Gene ID Gene Symbol Description Source
3482 IGF2R insulin like growth factor 2 receptor
3635 INPP5D inositol polyphosphate-5-phosphatase D
3958 LGALS3 galectin 3
4190 MDH1 malate dehydrogenase 1
4594 MMUT methylmalonyl-CoA mutase
4684 NCAM1 neural cell adhesion molecule 1
4967 OGDH oxoglutarate dehydrogenase
5223 PGAM1 phosphoglycerate mutase 1
5290 PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha
5291 PIK3CB phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta
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 11 - 20 of 58 in total
HPO ID HPO Term
HP:0000741 Apathy
HP:0000746 Delusion
HP:0000751 Personality changes
HP:0001250 Seizure
HP:0001289 Confusion
HP:0001324 Muscle weakness
HP:0001336 Myoclonus
HP:0001337 Tremor
HP:0001350 Slurred speech
HP:0002066 Gait ataxia
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