Medical Subject Headings

Last uploaded: August 27, 2019
Preferred Name

Creutzfeldt-Jakob Syndrome

Synonyms

Disease, Familial Creutzfeldt-Jakob

Definitions

A rare transmissible encephalopathy most prevalent between the ages of 50 and 70 years. Affected individuals may present with sleep disturbances, personality changes, ATAXIA; APHASIA, visual loss, weakness, muscle atrophy, MYOCLONUS, progressive dementia, and death within one year of disease onset. A familial form exhibiting autosomal dominant inheritance and a new variant CJD (potentially associated with ENCEPHALOPATHY, BOVINE SPONGIFORM) have been described. Pathological features include prominent cerebellar and cerebral cortical spongiform degeneration and the presence of PRIONS. (From N Engl J Med, 1998 Dec 31;339(27))

ID

http://purl.bioontology.org/ontology/MESH/D007562

altLabel

Disease, Familial Creutzfeldt-Jakob

Creutzfeldt Jakob Disease, New Variant

Disease, Creutzfeldt Jacob

CJD (Creutzfeldt Jakob Disease)

Creutzfeldt-Jakob Disease, Variant

Creutzfeldt-Jakob Diseases, Familial

Variant Creutzfeldt-Jakob Disease

Spongiform Encephalopathy, Subacute

Disease, Creutzfeldt-Jakob

Syndrome, Creutzfeldt-Jakob

Creutzfeldt-Jakob Disease, Familial

Creutzfeldt Jakob Disease

Creutzfeldt Jakob Disease, Familial

V-CJD (Variant-Creutzfeldt-Jakob Disease)

Familial Creutzfeldt Jakob Disease

Syndrome, Jakob-Creutzfeldt

Creutzfeldt Jakob Syndrome

Familial Creutzfeldt-Jakob Diseases

Jakob-Creutzfeldt Syndrome

Creutzfeldt-Jakob Disease, New Variant

Jakob-Creutzfeldt Disease

CJD (Creutzfeldt-Jakob Disease)

Familial Creutzfeldt-Jakob Disease

Subacute Spongiform Encephalopathies

Disease, Jakob-Creutzfeldt

Jacob Disease, Creutzfeldt

Jakob Creutzfeldt Disease

V CJD (Variant Creutzfeldt Jakob Disease)

Spongiform Encephalopathies, Subacute

Creutzfeldt Jacob Disease

New Variant Creutzfeldt-Jakob Disease

Jakob Creutzfeldt Syndrome

Encephalopathies, Subacute Spongiform

Subacute Spongiform Encephalopathy

Encephalopathy, Subacute Spongiform

Variant Creutzfeldt Jakob Disease

Creutzfeldt-Jakob Disease

Creutzfeldt Jakob Disease, Variant

New Variant Creutzfeldt Jakob Disease

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

C0376329

C0751254

C0022336

DC

1

definition

A rare transmissible encephalopathy most prevalent between the ages of 50 and 70 years. Affected individuals may present with sleep disturbances, personality changes, ATAXIA; APHASIA, visual loss, weakness, muscle atrophy, MYOCLONUS, progressive dementia, and death within one year of disease onset. A familial form exhibiting autosomal dominant inheritance and a new variant CJD (potentially associated with ENCEPHALOPATHY, BOVINE SPONGIFORM) have been described. Pathological features include prominent cerebellar and cerebral cortical spongiform degeneration and the presence of PRIONS. (From N Engl J Med, 1998 Dec 31;339(27))

DX

19730101

HN

1991; use JAKOB-CREUTZFELDT SYNDROME 1981-1990, use CREUTZFELDT-JAKOB DISEASE 1969-1980

Inverse of AQ

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

http://purl.bioontology.org/ontology/MESH/Q000150

http://purl.bioontology.org/ontology/MESH/Q000188

http://purl.bioontology.org/ontology/MESH/Q000517

http://purl.bioontology.org/ontology/MESH/Q000201

http://purl.bioontology.org/ontology/MESH/Q000145

http://purl.bioontology.org/ontology/MESH/Q000503

http://purl.bioontology.org/ontology/MESH/Q000453

http://purl.bioontology.org/ontology/MESH/Q000208

http://purl.bioontology.org/ontology/MESH/Q000134

http://purl.bioontology.org/ontology/MESH/Q000821

http://purl.bioontology.org/ontology/MESH/Q000382

http://purl.bioontology.org/ontology/MESH/Q000601

http://purl.bioontology.org/ontology/MESH/Q000235

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

http://purl.bioontology.org/ontology/MESH/Q000276

http://purl.bioontology.org/ontology/MESH/Q000191

http://purl.bioontology.org/ontology/MESH/Q000652

http://purl.bioontology.org/ontology/MESH/Q000662

http://purl.bioontology.org/ontology/MESH/Q000151

http://purl.bioontology.org/ontology/MESH/Q000628

http://purl.bioontology.org/ontology/MESH/Q000196

http://purl.bioontology.org/ontology/MESH/Q000534

http://purl.bioontology.org/ontology/MESH/Q000635

http://purl.bioontology.org/ontology/MESH/Q000266

http://purl.bioontology.org/ontology/MESH/Q000532

http://purl.bioontology.org/ontology/MESH/Q000139

http://purl.bioontology.org/ontology/MESH/Q000378

http://purl.bioontology.org/ontology/MESH/Q000175

http://purl.bioontology.org/ontology/MESH/Q000000981

http://purl.bioontology.org/ontology/MESH/Q000097

http://purl.bioontology.org/ontology/MESH/Q000473

http://purl.bioontology.org/ontology/MESH/Q000451

http://purl.bioontology.org/ontology/MESH/Q000209

http://purl.bioontology.org/ontology/MESH/Q000178

http://purl.bioontology.org/ontology/MESH/Q000469

Inverse of SIB

http://purl.bioontology.org/ontology/MESH/D006816

http://purl.bioontology.org/ontology/MESH/D034062

http://purl.bioontology.org/ontology/MESH/D020232

http://purl.bioontology.org/ontology/MESH/D016098

http://purl.bioontology.org/ontology/MESH/D016643

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

http://purl.bioontology.org/ontology/MESH/D055956

http://purl.bioontology.org/ontology/MESH/D057174

http://purl.bioontology.org/ontology/MESH/D015140

http://purl.bioontology.org/ontology/MESH/D007729

http://purl.bioontology.org/ontology/MESH/D018888

http://purl.bioontology.org/ontology/MESH/D020961

http://purl.bioontology.org/ontology/MESH/D000544

http://purl.bioontology.org/ontology/MESH/D034081

http://purl.bioontology.org/ontology/MESH/D015526

Machine permutation

1991; see JAKOB-CREUTZFELDT SYNDROME 1981-1990, see CREUTZFELDT-JAKOB DISEASE 1973-1980

Mapped from

http://purl.bioontology.org/ontology/MESH/C538481

http://purl.bioontology.org/ontology/MESH/C565143

http://purl.bioontology.org/ontology/MESH/C566981

MDA

19990101

MMR

20150603

MN

C10.228.228.800.230

C10.228.140.380.165

F03.615.400.300

notation

D007562

prefLabel

Creutzfeldt-Jakob Syndrome

TERMUI

T022729

T367209

T022732

T752045

T022734

T367208

T367207

T022730

T367210

T812338

T022731

T367205

T752046

T367204

TH

NLM (1991)

UNK (19XX)

NLM (2000)

NLM (2010)

ORD (2010)

NLM (1997)

OMIM (2013)

NLM (1969)

tui

T047

subClassOf

http://purl.bioontology.org/ontology/MESH/D003704

http://purl.bioontology.org/ontology/MESH/D017096

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http://purl.bioontology.org/ontology/MDRFRE/10023116 MDRFRE CUI
http://ontology.apa.org/apaonto/termsonlyOUT%20(5).owl#Creutzfeldt_Jakob_Syndrome APANEUROCLUSTER LOOM
http://ontology.apa.org/apaonto/termsonlyOUT%20(5).owl#Creutzfeldt_Jakob_Syndrome APAONTO LOOM
http://ontology.apa.org/apaonto/termsonlyOUT%20(5).owl#Creutzfeldt_Jakob_Syndrome APADISORDERS LOOM
http://purl.bioontology.org/ontology/WHOFRE/1527 WHOFRE CUI
http://purl.bioontology.org/ontology/SNMI/DE-3B020 SNMI CUI
http://purl.bioontology.org/ontology/ICD9CM/046.1 ICD9CM CUI
http://purl.bioontology.org/ontology/WHO/1527 WHO-ART CUI
http://purl.bioontology.org/ontology/SNMI/DE-36210 SNMI CUI
http://purl.bioontology.org/ontology/OMIM/176640 OMIM CUI
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.228.140.380.165 RH-MESH LOOM
http://purl.bioontology.org/ontology/CSP/2042-5006 CRISP CUI
http://sbmi.uth.tmc.edu/ontology/ochv#6985 OCHV LOOM
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0376329 MEDLINEPLUS CUI
http://purl.bioontology.org/ontology/ICD10/A81.0 ICD10 CUI
http://purl.bioontology.org/ontology/MDRFRE/10023117 MDRFRE CUI
http://purl.bioontology.org/ontology/MEDDRA/10009217 MEDDRA CUI
http://purl.bioontology.org/ontology/MEDDRA/10023116 MEDDRA CUI
http://purl.bioontology.org/ontology/NDFRT/N0000001713 NDFRT CUI
http://purl.bioontology.org/ontology/MSHFRE/D007562 MSHFRE CUI
http://purl.bioontology.org/ontology/MSHFRE/D007562 MSHFRE CUI
http://purl.bioontology.org/ontology/MSHFRE/D007562 MSHFRE CUI
http://purl.bioontology.org/ontology/RCD/XaA1S RCD CUI
http://purl.bioontology.org/ontology/MDRFRE/10009216 MDRFRE CUI
http://bioontology.org/projects/ontologies/birnlex#birnlex_12687 BIRNLEX LOOM
http://purl.bioontology.org/ontology/MDRFRE/10055172 MDRFRE CUI
http://purl.bioontology.org/ontology/ICD10CM/A81.09 ICD10CM CUI
http://purl.bioontology.org/ontology/MDRFRE/10064199 MDRFRE CUI
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D007562 RH-MESH LOOM
http://www.owl-ontologies.com/NPOntology.owl#DOID_11949 NATPRO LOOM
http://purl.bioontology.org/ontology/MDRFRE/10011382 MDRFRE CUI
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0022336 MEDLINEPLUS CUI
http://purl.bioontology.org/ontology/MDRFRE/10011384 MDRFRE CUI
http://purl.bioontology.org/ontology/SNOMEDCT/304603007 SNOMEDCT CUI
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.228.228.800.230 RH-MESH LOOM
http://purl.bioontology.org/ontology/RCD/A411. RCD CUI
http://purl.bioontology.org/ontology/ICD10CM/A81.0 ICD10CM CUI
http://purl.bioontology.org/ontology/SCTSPA/304603007 SCTSPA CUI
http://purl.bioontology.org/ontology/MEDDRA/10011384 MEDDRA CUI
http://purl.bioontology.org/ontology/SNOMEDCT/792004 SNOMEDCT CUI
http://uri.neuinfo.org/nif/nifstd/birnlex_12687 NIFDYS LOOM
http://uri.neuinfo.org/nif/nifstd/birnlex_12687 NIFSTD LOOM
http://purl.bioontology.org/ontology/MEDDRA/10009216 MEDDRA CUI
http://purl.bioontology.org/ontology/MEDDRA/10023117 MEDDRA CUI
http://phenomebrowser.net/ontologies/mesh/mesh.owl#F03.087.400.300 RH-MESH LOOM
http://purl.bioontology.org/ontology/OMIM/123400 OMIM CUI
http://purl.bioontology.org/ontology/OMIM/123400 OMIM CUI
http://purl.bioontology.org/ontology/OMIM/123400 OMIM CUI
http://purl.bioontology.org/ontology/ICD10CM/A81.00 ICD10CM CUI
http://purl.bioontology.org/ontology/ICD9CM/046.11 ICD9CM CUI
http://purl.bioontology.org/ontology/MEDDRA/10011382 MEDDRA CUI
http://purl.bioontology.org/ontology/MDRFRE/10009217 MDRFRE CUI
http://purl.bioontology.org/ontology/MEDDRA/10064199 MEDDRA CUI
http://purl.bioontology.org/ontology/SCTSPA/792004 SCTSPA CUI
http://purl.bioontology.org/ontology/ICD10CM/A81.01 ICD10CM CUI
http://purl.bioontology.org/ontology/MEDDRA/10055172 MEDDRA CUI