serw-MX  [xml]  
 


    
 DeCS Categories

C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.228 Central Nervous System Infections .
C10.228.228.800 Prion Diseases .
C10.574 Neurodegenerative Diseases .
C10.574.843 Prion Diseases .
C25 Chemically-Induced Disorders .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Chemically-Induced Disorders .
Chemically Induced Disorders .
Chemically-Induced Disorder .
Disorder, Chemically-Induced .
Disorders, Chemically-Induced .
Disorders caused by the intentional or unintentional ingestion or exposure to chemical substances such as PHARMACEUTICAL PREPARATIONS; NOXAE; and PESTICIDES. .
1.00
021
 
/chemically induced .
Used for biological phenomena, diseases, syndromes, congenital abnormalities, or symptoms caused by endogenous or exogenous substances. .
0.82
 
Prion Diseases .
Encephalopathies, Spongiform, Transmissible .
Human Transmissible Spongiform Encephalopathies, Inherited .
Inherited Human Transmissible Spongiform Encephalopathies .
Prion Disease .
Prion Protein Diseases .
Prion-Associated Disorders .
Prion-Induced Disorder .
Prion-Induced Disorders .
Transmissible Spongiform Encephalopathies .
Dementia, Transmissible .
Disorder, Prion-Induced .
Disorders, Prion-Induced .
Encephalopathies, Transmissible Spongiform .
Encephalopathy, Transmissible Spongiform .
Prion Induced Disorder .
Prion Protein Disease .
Spongiform Encephalopathy, Transmissible .
Transmissible Dementia .
Transmissible Spongiform Encephalopathy .
Dementias, Transmissible .
Spongiform Encephalopathies, Transmissible .
Transmissible Dementias .
ENCEPHALOPATHIES, SPONGIFORM .
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) .
0.67
654101