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Familial Creutzfeldt-Jakob Disease
| Name: | Familial Creutzfeldt-Jakob Disease |
| Description: | A familial form exhibiting autosomal dominant inheritance has been described. Pathological features include prominent cerebellar and cerebral cortical spongiform degeneration and the presence of PRIONS (MeSH). |
| Super-category: | Creutzfeldt-Jakob Syndrome |
| URL: | N Engl J Med, 1998 Dec 31;339(27) |
| Id: | birnlex_12688 |
| Link to OWL / RDF: | Download this content as OWL/RDF |
- Definition Source: MeSH
Facts about Familial Creutzfeldt-Jakob DiseaseRDF feed
| Created | 5 October 2007 + |
| CurationStatus | uncurated + |
| DefiningCitation | N Engl J Med, 1998 Dec 31;339(27) + |
| Definition | A familial form exhibiting autosomal dominant inheritance has been described. Pathological features include prominent cerebellar and cerebral cortical spongiform degeneration and the presence of PRIONS (MeSH). |
| DefinitionSource | MeSH + |
| Id | birnlex_12688 + |
| Label | Familial Creutzfeldt-Jakob Disease + |
| ModifiedDate | 30 May 2009 + |
| SuperCategory | Creutzfeldt-Jakob Syndrome + |