UFSP, Malattie > Panoramica delle malattie > Malattia di Creutzfeldt-Jakob ([Internet, 2024-12-04](https://www.bag.admin.ch/bag/it/home/krankheiten/krankheiten-im-ueberblick/cjk.html))
(fCJK) 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)); (fCJD) AT, Bundesministerium Soziales, Gesundheit, Pflege und Konsumentenschutz, Creutzfeldt-Jakob-Krankheit, 2024-07-23 ([Internet, 2024-12-04](https://www.sozialministerium.at/Themen/Gesundheit/Uebertragbare-Krankheiten/Infektionskrankheiten-A-Z/Creutzfeldt-Jakob-Krankheit.html))
(MCJf) OFSP, Maladies > Maladies : vue d’ensemble > Maladie de Creutzfeldt-Jakob ([Internet, 2024-12-04](https://www.bag.admin.ch/bag/fr/home/krankheiten/krankheiten-im-ueberblick/cjk.html)); (fCJD) FOPH, Diseases > Diseases from A to Z > Creutzfeldt-Jakob Disease (CJD) ([Internet, 2024-12-09](https://www.bag.admin.ch/bag/en/home/krankheiten/krankheiten-im-ueberblick/cjk.html))
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))
EXP: familiär vererbbare Form der Creutzfeldt-Jakob-Krankheit, die sich bereits mit 50 Jahren bemerkbar machen kann
EXP: "fMCJ" est l'abréviation de l'anglais "familial Creutzfeldt-Jakob Disease"
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
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
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))
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))
(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))