prion disease
Information
- Disease name
- prion disease
- Disease ID
- DOID:649
- Description
- "A brain disease that is characterized by brain damage resulting from the abnormal folding, clumping and accumulation of cellular proteins in the brain induced by prion proteins." [url:http\://en.wikipedia.org/wiki/Prion, url:http\://www.cdc.gov/ncidod/dvrd/prions/]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT06153966 | Active, not recruiting | Phase 1/Phase 2 | PrProfile: A Study to Assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of ION717. | January 4, 2024 | October 2025 |
| NCT00104663 | Completed | N/A | PRION-1: Quinacrine for Human Prion Disease | June 2004 | March 2007 |
| NCT02629640 | Completed | Enhanced CJD Surveillance in the Older Population | January 19, 2016 | March 31, 2022 |
- Disase is a (Disease Ontology)
- DOID:936
- Cross Reference ID (Disease Ontology)
- ICD10CM:A81.9
- Cross Reference ID (Disease Ontology)
- KEGG:05020
- Cross Reference ID (Disease Ontology)
- MESH:D017096
- Cross Reference ID (Disease Ontology)
- NCI:C128346
- Cross Reference ID (Disease Ontology)
- SNOMEDCT_US_2023_03_01:20484008
- Cross Reference ID (Disease Ontology)
- UMLS_CUI:C0162534
- Exact Synonym (Disease Ontology)
- Prion disease pathway
- Exact Synonym (Disease Ontology)
- prion induced disorder
- Exact Synonym (Disease Ontology)
- Prion protein disease
- Exact Synonym (Disease Ontology)
- Spongiform Encephalopathy
- Exact Synonym (Disease Ontology)
- transmissible spongiform encephalopathy