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Attributes

seltene Krankheit
rare disease
maladie rare
malattia rara
Krankheit, die höchstens fünf von 10'000 Personen betrifft und die lebensbedrohlich oder chronisch invalidisierend ist.
Diseases that affects a small number of people compared to the general population.
Maladie qui touche au maximum 5 personnes sur 10'000, et qui est potentiellement mortelle ou entraîne une invalidité chronique.
Malattia che colpisce al massimo cinque persone su 10 000 e che è potenzialmente mortale o provoca un'invalidità cronica.
2018-09-03T14:24:56.3030000Z
387313
https://www.termdat.bk.admin.ch/entry/387313
BAG, PM Nationales Konzept Seltene Krankheiten: Genehmigung der Umsetzungsplanung, 2015-05-13 ([Internet, 2015-08-31](https://www.admin.ch/gov/de/start/dokumentation/medienmitteilungen.msg-id-57239.html))
Health on the Net Foundation, Rare Diseases, 2009 ([Internet, 2015-08-31](http://www.hon.ch/SR/C23.550.291.906_en.html))
OFSP, Comm. pr. Concept national maladies rares : Approbation du plan de mise en œuvre, 2015-05-13 ([Internet, 2015-08-31](https://www.admin.ch/gov/fr/accueil/documentation/communiques.msg-id-57239.html))
UFSP, CS Programma nazionale malattie rare: approvato il piano d’attuazione per concretizzarlo, 2015-05-13 ([Internet, 2015-08-31](https://www.admin.ch/gov/it/pagina-iniziale/documentazione/comunicati-stampa.msg-id-57239.html))
EXP: in der Schweiz leiden schätzungsweise bis zu 580 000 Personen an einer seltenen Krankheit; oft vergeht viel Zeit, bis eine korrekte Diagnose gestellt wird und die Erkrankten eine angemessene Behandlung erhalten
EXP: a rare disease occurs in less than 5 per 10,000 individuals in the European Union; some diseases are widespread in certain parts of the world but rare in others
EXP: on estime que près de 580 000 personnes pourraient en souffrir en Suisse; ces personnes endurent bien souvent avec leurs proches une longue course d'obstacles avant qu'un diagnostic correct ne soit posé et qu'elles puissent recevoir le traitement approprié
USG: da non confondere con «malattia orfana»; EXP: molte malattie rare sono anche orfane; tuttavia alcune malattie rare hanno ricevuto un’attenzione significativa, che ha suscitato attività di ricerca puntuale, dalla quale sono derivate terapie adeguate, cosicché non possono più essere considerate orfane
nach BAG, PM Nationales Konzept Seltene Krankheiten: Genehmigung der Umsetzungsplanung, 2015-05-13 ([Internet, 2015-08-31](https://www.admin.ch/gov/de/start/dokumentation/medienmitteilungen.msg-id-57239.html))
after Health on the Net Foundation, Rare Diseases, 2009 ([Internet, 2015-08-31](http://www.hon.ch/SR/C23.550.291.906_en.html))
d'après OFSP, Comm. pr. Concept national maladies rares : Approbation du plan de mise en œuvre, 2015-05-13 ([Internet, 2015-08-31](https://www.admin.ch/gov/fr/accueil/documentation/communiques.msg-id-57239.html))
European Respiratory Society, European Lung White Book, cap. 25 «Malattie respiratorie rare e orfane», p. 297-298 ([Internet, 2016-03-03](http://www.erswhitebook.org/files/public/Italian%20PDFs/25.Orphan%20lung%20diseases.pdf))
Health on the Net Foundation, Rare Diseases, 2009 ([Internet, 2015-08-31](http://www.hon.ch/SR/C23.550.291.906_en.html))
OFSP, Comm. pr. Concept national maladies rares : Approbation du plan de mise en œuvre, 2015-05-13 ([Internet, 2015-08-31](https://www.admin.ch/gov/fr/accueil/documentation/communiques.msg-id-57239.html))
nach BAG, PM Nationales Konzept Seltene Krankheiten: Genehmigung der Umsetzungsplanung, 2015-05-13 ([Internet, 2015-08-31](https://www.admin.ch/gov/de/start/dokumentation/medienmitteilungen.msg-id-57239.html))
secondo UFSP, CS Programma nazionale malattie rare: approvato il piano d’attuazione per concretizzarlo, 2015-05-13 ([Internet, 2015-08-31](https://www.admin.ch/gov/it/pagina-iniziale/documentazione/comunicati-stampa.msg-id-57239.html))
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