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SELECT ?title WHERE { ?? (rdfs:label|skos:prefLabel|schema:name) ?title . } familiäre Creutzfeldt-Jakob-Krankheit

SELECT ?class WHERE { ?? (rdf:type|owl:type) ?class . } DefinedTerm, Term, Validated Entry

SELECT ?description WHERE { ?? (rdfs:comment|schema:description) ?description . }

SELECT ?property ?value WHERE { BIND (?? AS ?s) ?s ?property ?value . FILTER (isLiteral(?value)) } LIMIT 1000

Attributes

Name
familiäre Creutzfeldt-Jakob-Krankheit
Name
maladie de Creutzfeldt-Jakob familiale
Name
malattia di Creutzfeldt-Jakob familiare
Name
familial Creutzfeldt–Jakob disease
dateModified
2025-07-28T06:02:12.2913510Z
Identifier
515716
Alternate name
fCJD
Alternate name
fMCJ
Alternate name
fCJK, fCJD
Alternate name
MCJf; fCJD
URL
https://www.termdat.bk.admin.ch/entry/515716
citation
Manuel MSD, Professisonnels > Troubles neurologiques > Maladies à prions > Maladie de Creutzfeldt-Jakob ([Internet, 2024-12-10](https://www.msdmanuals.com/fr/professional/troubles-neurologiques/maladies-%C3%A0-prions/maladie-de-creutzfeldt-jakob))
citation
Manuale MSD, Professionisti > Malattie neurologiche > Malattie prioniche > Malattia di Creutzfeldt-Jakob ([Internet, 2024-12-10](https://www.msdmanuals.com/it/professionale/malattie-neurologiche/malattie-prioniche/malattia-di-creutzfeldt-jakob))
citation
MGZ, Diagnostik > Erkrankungen > Neurogenetische Erkrankungen/Ataxie > Prion-Erkrankungen, erblich bedingt ([Internet, 2025-01-07](https://www.mgz-muenchen.de/erkrankungen/diagnose/prion-erkrankungen-erblich-bedingt.html#:~:text=Famili%C3%A4re%20Creuzfeldt%2DJakob%2DKrankheit%20%28,%2C%20progrediente%20Dysarthrie%29%20und%20Myoklonus.))
citation
Physiopedia, Prion Diseases (or Transmissible Spongiform Encephalopathies) ([Internet, 2025-07-11](https://www.physio-pedia.com/Prion_Diseases_%28or_Transmissible_Spongiform_Encephalopathies%29?et_blog&utm_source=meta&utm_medium=cpc&utm_campaign=landing-deporte&fbclid=IwZXh0bgNhZW0BMAABHXzdVJdpQDdpA3h6Nraw22tJ7EvYxGe1sFe7HVXyLGT4FQZKjWVHs0pRsA_aem_hyB9Oi23rwSlDFmWKf0ArQ&utm_id=6630696416988&utm_content=6630872179788&utm_term=6630696417388))
position
1
Term Note
EXP: familiär vererbbare Form der Creutzfeldt-Jakob-Krankheit, die sich bereits mit 50 Jahren bemerkbar machen kann
Term Note
EXP: "fMCJ" est l'abréviation de l'anglais "familial Creutzfeldt-Jakob Disease"
Term Note
EXP: causata da un'anomalia di uno dei due geni della proteina prionica cellulare che una persona eredita dai propri genitori; questa anomalia (mutazione) favorisce la formazione del prione nel cervello durante l'età adulta dando luogo ai sintomi della malattia, che di solito si sviluppano intorno ai 50-55 anni di età
Term Note
USG: the term is usually written with "disease" in lowercase: "familial Creutzfeldt–Jakob disease"; capitalisation of "Disease" is also occasionally seen: "familial Creutzfeldt–Jakob Disease"; EXP: the tendency to develop pathogenic prions is inherited and cases of fCJD can manifest themselves from age 50 onwards
termNoteCitation
nach MeinMed.at, Krankheiten von A bis Z > Neurologie und Psychiatrie > Creutzfeldt-Jakob-Erkrankung ([Internet, 2025-01-07](https://www.meinmed.at/krankheit/creutzfeldt-jakob-krankheit/1904)) und BAG, Krankheiten > Krankheiten im Überblick > Creutzfeldt-Jakob-Krankheit ([Internet, 2024-12-04](https://www.bag.admin.ch/bag/de/home/krankheiten/krankheiten-im-ueberblick/cjk.html))
termNoteCitation
secondo IT, Istituto superiore di Sanità ISS, ISSalute, Malattia di Creutzfeldt-Jacob (MCJ) ([Internet, 2025-03-12](https://www.issalute.it/index.php/la-salute-dalla-a-alla-z-menu/m/malattia-di-creutzfeldt-jacob-mcj))
termNoteCitation
(USG) FCh, English Language Service, 2025; (EXP) after FOPH, Creutzfeldt-Jakob Disease (CJD), 2024-07-06 ([Internet, 2025-07-11](https://www.bag.admin.ch/en/creutzfeldt-jakob-disease-cjd))
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Outgoing Relationships

property object
inDefinedTermSet Terminology of medicine (anatomy, pathology)
inDefinedTermSet Swiss Federal Administration
has part genetische Creutzfeldt-Jakob-Krankheit
has part maladie de Creutzfeldt-Jakob d'origine génétique
has part forma familiare della malattia di Creutzfeldt-Jakob
has part familiäre Form der Creutzfeldt-Jakob-Erkrankung
has part fCJD
has part MCJ familiale
has part familiäre CJK
has part malattia di Creutzfeldt-Jacob genetica
hypernym Creutzfeldt–Jakob disease
Reliability code Linguistic/formal check completed
termDomain MEDICINE
termDomain Pathology
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Incoming Relationships

property subject
hyponym Creutzfeldt–Jakob disease
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