Presenter: Grant Wood Member, HL7 Clinical Genomics Work Group; Co-Chair, HL7 Marketing Council; Senior IT Strategist, Intermountain Healthcare's Clinical Genomics Institute

This webinar will cover the HL7 Family History Model, interoperability between patient entered and clinical information systems, and its mapping between the different classes in the model (person of focus, other persons, disease, genotypic data, and risk analysis) and the requirements stated by MU Stage 2 for exchange.

Audience & Benefits
Implementers of exchange or data collection for Family Pedigree will gain an understanding of how to read the V3 Family History Model specification and MU Stage 2 related specifications.

Objectives
Upon completion of this webinar, attendees will be able to:

• Discuss personalized Medical History; value of family history in clinical care, and current methods of data collection.
• Describe the HL7 Family History Data Model, what's inside, data to transmit and display genetic results in XML.
• Provide value sets, and use the Nomenclature and Code System for MU Stage 2 Pedigree Exchange

Requirements addressed
Clinical Requirements: §170.314(a)(13)