Plain-language medical vocabulary for precision diagnosis

For undiagnosed patients and those with rare diseases, the affected individuals themselves are an especially critical source of phenotyping information. These patients live with their condition and develop explicit and implicit knowledge about it, whether from multiple clinician evaluations or from...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Nature genetics 2018-04, Vol.50 (4), p.474-476
Hauptverfasser: Vasilevsky, Nicole A., Foster, Erin D., Engelstad, Mark E., Carmody, Leigh, Might, Matt, Chambers, Chip, Dawkins, Hugh J. S., Lewis, Janine, Della Rocca, Maria G., Snyder, Michelle, Boerkoel, Cornelius F., Rath, Ana, Terry, Sharon F., Kent, Alastair, Searle, Beverly, Baynam, Gareth, Jones, Erik, Gavin, Pam, Bamshad, Michael, Chong, Jessica, Groza, Tudor, Adams, David, Resnick, Adam C., Heath, Allison P., Mungall, Chris, Holm, Ingrid A., Rageth, Kayli, Brownstein, Catherine A., Shefchek, Kent, McMurry, Julie A., Robinson, Peter N., Köhler, Sebastian, Haendel, Melissa A.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:For undiagnosed patients and those with rare diseases, the affected individuals themselves are an especially critical source of phenotyping information. These patients live with their condition and develop explicit and implicit knowledge about it, whether from multiple clinician evaluations or from other families and patients experiencing diagnosis for similar conditions. From these interactions, they develop a lexicon of relevant terms; these terms are frequently in plain language, but can also include clinical terms.
ISSN:1061-4036
1546-1718
1546-1718
DOI:10.1038/s41588-018-0096-x