Assessing the Hereditary Hemorrhagic Telangiectasia Algorithms in a Community-Based Patient Population

INTRODUCTION: Hereditary hemorrhagic telangiectasia (HHT) is a rare, genetic, and underdiagnosed disease that causes vascular malformations throughout the body. Two specific combinations of International Classification of Diseases, Ninth Revision-Clinical Modification diagnosis codes, the “HHT Algor...

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Bibliografiska uppgifter
I publikationen:Perm J
Huvudupphovsmän: Saparia, Tina, Faughnan, Marie E, Schneider, Jennifer L, Almers, Lucy M, Chow, Norma, Grosse, Scott D, Kim, Helen, Zaroff, Jonathan G
Materialtyp: Artigo
Språk:Inglês
Publicerad: The Permanente Journal 2019
Ämnen:
Original Research & Contributions
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC6443364/
https://ncbi.nlm.nih.gov/pubmed/30939282
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7812/TPP/18-145
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