Mucopolysaccharidosis type II detection by Naïve Bayes Classifier: An example of patient classification for a rare disease using electronic medical records from the Canadian Primary Care Sentinel Surveillance Network

Identifying patients with rare diseases associated with common symptoms is challenging. Hunter syndrome, or Mucopolysaccharidosis type II is a progressive rare disease caused by a deficiency in the activity of the lysosomal enzyme, iduronate 2-sulphatase. It is inherited in an X-linked manner result...

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Detalles Bibliográficos
Autores principales: Ehsani-Moghaddam, Behrouz, Queenan, John A., MacKenzie, Jennifer, Birtwhistle, Richard V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6300265/
https://www.ncbi.nlm.nih.gov/pubmed/30566525
http://dx.doi.org/10.1371/journal.pone.0209018

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6300265/
https://www.ncbi.nlm.nih.gov/pubmed/30566525
http://dx.doi.org/10.1371/journal.pone.0209018

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