PhenoTips is a tool for collecting and analyzing phenotypic information for patients with genetic disorders. It combines an easy-to-use interface, compatible with any device which runs a Web browser, with a standardized database backend. The PhenoTips user interface closely mirrors clinician workflows, to facilitate the recording of observations made during the patient encounter. By collecting, classifying, and analyzing phenotypic information during the patient encounter, PhenoTips allows streamlining of clinic workflow, efficient data entry, improved diagnosis, standardization of collected patient phenotypes, and sharing of anonymized patient phenotype data for the study of rare disorders.
|Tags||Web Computational Medicine Phenotyping|
|Operating Systems||all Java capable systems|
Release Notes: This is a quick bugfix release addressing another important regression detected in the 1.0 Milestone 12 release.
Release Notes: This is a quick bugfix release addressing 3 regressions detected in the 1.0 Milestone 12 release.
Release Notes: This is a mostly bugfix release with few new features. Hopefully, this is the last milestone before the 1.0 release candidate. The highlights of this release are better similarity score computation, improved JSON and CSV exportation, and pedigree editor improvements.
Release Notes: The highlights of this release are an improved patient report UI, support for pushing patient records to other instances, a specificity metric widget, better gene list UI, a default list of ethnicities, pedigree improvements, a new RPM package, and many other UI improvements.
Release Notes: Many bugfixes and improvements making PhenoTips easier to use in a collaborative environment. The highlights of this release are an improved homepage, pedigree drawing enabled by default, redesigned administration, and support for disease studies.