Preferred Name |
Prion Diseases |
|
Synonyms |
Transmissible Spongiform Encephalopathies Prion Disease |
|
Definitions |
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) |
|
ID |
http://purl.bioontology.org/ontology/MESH/D017096 |
|
altLabel |
Transmissible Spongiform Encephalopathies Disorders, Prion-Induced Dementias, Transmissible Transmissible Dementias Inherited Human Transmissible Spongiform Encephalopathies Prion Induced Disorder Encephalopathy, Transmissible Spongiform Spongiform Encephalopathy, Transmissible Dementia, Transmissible Prion-Induced Disorders Prion Protein Disease Disorder, Prion-Induced Transmissible Dementia Encephalopathies, Spongiform, Transmissible Human Transmissible Spongiform Encephalopathies, Inherited Prion Protein Diseases Prion-Associated Disorders Prion-Induced Disorder Transmissible Spongiform Encephalopathy Spongiform Encephalopathies, Transmissible Encephalopathies, Transmissible Spongiform Prion Disease |
|
AN |
general or unspecified; prefer specifics |
|
AQL |
BL CF CI CL CN CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH TM UR VE VI |
|
cui |
C0751645 C0162534 |
|
DC |
1 |
|
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) |
|
DX |
19930101 |
|
HN |
1993 |
|
Inverse of AQ |
http://purl.bioontology.org/ontology/MESH/Q000097 http://purl.bioontology.org/ontology/MESH/Q000178 http://purl.bioontology.org/ontology/MESH/Q000175 http://purl.bioontology.org/ontology/MESH/Q000628 http://purl.bioontology.org/ontology/MESH/Q000276 http://purl.bioontology.org/ontology/MESH/Q000134 http://purl.bioontology.org/ontology/MESH/Q000139 http://purl.bioontology.org/ontology/MESH/Q000266 http://purl.bioontology.org/ontology/MESH/Q000378 http://purl.bioontology.org/ontology/MESH/Q000517 http://purl.bioontology.org/ontology/MESH/Q000662 http://purl.bioontology.org/ontology/MESH/Q000469 http://purl.bioontology.org/ontology/MESH/Q000151 http://purl.bioontology.org/ontology/MESH/Q000150 http://purl.bioontology.org/ontology/MESH/Q000821 http://purl.bioontology.org/ontology/MESH/Q000191 http://purl.bioontology.org/ontology/MESH/Q000196 http://purl.bioontology.org/ontology/MESH/Q000473 http://purl.bioontology.org/ontology/MESH/Q000145 http://purl.bioontology.org/ontology/MESH/Q000382 http://purl.bioontology.org/ontology/MESH/Q000451 http://purl.bioontology.org/ontology/MESH/Q000453 http://purl.bioontology.org/ontology/MESH/Q000534 http://purl.bioontology.org/ontology/MESH/Q000532 http://purl.bioontology.org/ontology/MESH/Q000503 http://purl.bioontology.org/ontology/MESH/Q000188 http://purl.bioontology.org/ontology/MESH/Q000235 http://purl.bioontology.org/ontology/MESH/Q000201 http://purl.bioontology.org/ontology/MESH/Q000209 http://purl.bioontology.org/ontology/MESH/Q000208 http://purl.bioontology.org/ontology/MESH/Q000635 http://purl.bioontology.org/ontology/MESH/Q000601 http://purl.bioontology.org/ontology/MESH/Q000000981 http://purl.bioontology.org/ontology/MESH/Q000652 |
|
Inverse of RO | ||
Machine permutation |
1993 |
|
Mapped from | ||
MDA |
19920522 |
|
MMR |
20190617 |
|
MN |
C10.574.843 C10.228.228.800 C01.207.800 |
|
notation |
D017096 |
|
prefLabel |
Prion Diseases |
|
TERMUI |
T370039 T842325 T842327 T051045 T370038 T370040 T370037 T370041 T842326 T051042 T370036 T051044 T051043 |
|
TH |
NLM (2000) NLM (1993) GHR (2014) |
|
tui |
T047 |
|
subClassOf |