Online Population-Based Patient Registry to Collect and Share Health-related Data of Rare Disease Patients

Mizuki Morita, Soichi Ogishima, Kunihiro Nishimura, Eiji Aramaki, Tateo Ito. Online Population-Based Patient Registry to Collect and Share Health-related Data of Rare Disease Patients. In Data Driven Wellness: From Self-Tracking to Behavior Change, Papers from the 2013 AAAI Spring Symposium, Palo Alto, California, USA, March 25-27, 2013. Volume SS-13-03 of AAAI Technical Report, AAAI, 2013. [doi]

Abstract

Abstract is missing.