National Drug File - Reference Terminology - Prion Diseases [Disease/Finding] - Classes

Last uploaded: July 6, 2018

Id	http://purl.bioontology.org/ontology/NDFRT/N0000003530 http://purl.bioontology.org/ontology/NDFRT/N0000003530
Preferred Name	Prion Diseases [Disease/Finding]
Synonyms	Transmissible Spongiform Encephalopathies Dementias, Transmissible Transmissible Dementias Prion Diseases Prion-Induced Disorders Encephalopathies, Spongiform, Transmissible Prion Protein Diseases Prion-Associated Disorders Prion-Induced Disorder Spongiform Encephalopathies, Transmissible Prion Disease See more See less
Type	http://www.w3.org/2002/07/owl#Class

altLabel	Transmissible Spongiform Encephalopathies Dementias, Transmissible Transmissible Dementias Prion Diseases Prion-Induced Disorders Encephalopathies, Spongiform, Transmissible Prion Protein Diseases Prion-Associated Disorders Prion-Induced Disorder Spongiform Encephalopathies, Transmissible Prion Disease See more See less
prefLabel	Prion Diseases [Disease/Finding]
notation	N0000003530
MESH DEFINITION	A group of genetic, infectious, or sporadic degenerative human and animal nervous system disorders associated with abnormal PRIONS. These diseases are characterized by conversion of the normal prion protein to an abnormal configuration via a post-translational process. In humans, these conditions generally feature DEMENTIA; ATAXIA; and a fatal outcome. Pathologic features include a spongiform encephalopathy without evidence of inflammation. The older literature occasionally refers to these as unconventional SLOW VIRUS DISEASES. (From Proc Natl Acad Sci USA 1998 Nov 10;95(23):13363-83)
MESH UI	M0025975
subClassOf	http://purl.bioontology.org/ontology/NDFRT/N0000000710
Semantic type UMLS property	http://purl.bioontology.org/ontology/STY/T047
MeSH name	Prion Diseases
NDFRT kind	DISEASE_KIND
type	http://www.w3.org/2002/07/owl#Class
SNOMED CID	20484008 230284004
tui	T047
NUI	N0000003530
cui	C0162534
MESH DUI	D017096

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