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...
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Veröffentlicht in: | Nature genetics 2018-04, Vol.50 (4), p.474-476 |
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Hauptverfasser: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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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. |
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ISSN: | 1061-4036 1546-1718 1546-1718 |
DOI: | 10.1038/s41588-018-0096-x |