Collecting sexual orientation and gender identity data in electronic health records [electronic resource] : workshop summary / Joe Alper, Monica N. Feit, and Jon Q. Sanders, rapporteurs ; Board on the Health of Select Populations, Institute of Medicine of the National Academies.

Introduction and overview
Clinical rationale for collecting sexual orientation and gender identity data
Federal perspective on the use of electronic health records to collect sexual orientation and gender indentity data
Existing data collection practices in clinical settings
Developing and implementing questions for collecting data on sexual orientation and gender identity
Closing remarks.