Medical Subject Headings

Last uploaded: January 31, 2024
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

http://purl.bioontology.org/ontology/MESH/Q000523

http://purl.bioontology.org/ontology/MESH/Q000401

Inverse of RO

http://purl.bioontology.org/ontology/MESH/D012897

http://purl.bioontology.org/ontology/MESH/D012608

Machine permutation

1993

Mapped from

http://purl.bioontology.org/ontology/MESH/C535800

http://purl.bioontology.org/ontology/MESH/C564678

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

http://purl.bioontology.org/ontology/MESH/D002494

http://purl.bioontology.org/ontology/MESH/D019636

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http://purl.bioontology.org/ontology/MSHFRE/D017096 MSHFRE CUI
http://purl.bioontology.org/ontology/CSP/2042-5040 CRISP CUI
http://purl.bioontology.org/ontology/SNOMEDCT/20484008 SNOMEDCT CUI
http://purl.bioontology.org/ontology/LNC/LP173528-3 LOINC CUI
http://purl.bioontology.org/ontology/CSP/2042-5006 CRISP CUI
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0162534 MEDLINEPLUS CUI
http://purl.bioontology.org/ontology/MEDDRA/10080750 MEDDRA CUI
http://purl.bioontology.org/ontology/ICD10CM/A81.9 ICD10CM CUI
http://purl.bioontology.org/ontology/MEDDRA/10036760 MEDDRA CUI
http://purl.bioontology.org/ontology/MDRGER/10080750 MDRGER CUI
http://purl.bioontology.org/ontology/MDRFRE/10080750 MDRFRE CUI
http://purl.bioontology.org/ontology/SNMI/DE-3B000 SNMI CUI
http://purl.bioontology.org/ontology/RCD/X003L RCD CUI
http://purl.bioontology.org/ontology/MDRFRE/10079301 MDRFRE CUI
http://purl.bioontology.org/ontology/MDRGER/10036760 MDRGER CUI
http://purl.bioontology.org/ontology/MEDDRA/10079301 MEDDRA CUI
http://purl.bioontology.org/ontology/MDRGER/10079301 MDRGER CUI
http://purl.bioontology.org/ontology/LNC/MTHU046519 LOINC CUI
http://purl.bioontology.org/ontology/MSHFRE/D017096 MSHFRE CUI
http://purl.bioontology.org/ontology/MDRFRE/10036760 MDRFRE CUI
http://purl.bioontology.org/ontology/SCTSPA/20484008 SCTSPA CUI
http://purl.bioontology.org/ontology/NDFRT/N0000003530 NDFRT CUI
http://purl.obolibrary.org/obo/OMIT_0017503 OMIT LOOM
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0162534 MEDLINEPLUS LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#17879 OCHV LOOM
http://doe-generated-ontology.com/OntoAD#C0162534 ONTOAD LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.574.843 RH-MESH LOOM
http://www.phoc.org.cn/pmo/class/PMO_00036057 PMAPP-PMO LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.228.228.800 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D017096 RH-MESH LOOM
http://localhost/plosthes.2017-1#6052 PLOSTHES LOOM