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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

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Facts about Familial Creutzfeldt-Jakob DiseaseRDF feed
Created5 October 2007  +
CurationStatusuncurated  +
DefiningCitationN Engl J Med, 1998 Dec 31;339(27)  +
DefinitionA 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).
DefinitionSourceMeSH  +
Idbirnlex_12688  +
LabelFamilial Creutzfeldt-Jakob Disease  +
ModifiedDate30 May 2009  +
SuperCategoryCreutzfeldt-Jakob Syndrome  +