Ending the Diagnostic Odyssey Act of 2019
Official title: A bill to enable States to better provide access to whole genome sequencing clinical services for certain undiagnosed children under the Medicaid program, and for other purposes.
More subjectsShow fewer subjects
Have a question about what this bill does? Ask in plain English; the answer is drawn from the bill's actual text and official record, and it'll tell you when something isn't in the text rather than guess.
Read twice and referred to the Committee on Finance. (Sponsor introductory remarks on measure: CR S7211)
Ending the Diagnostic Odyssey Act of 2019
This bill allows state Medicaid programs to cover whole genome sequencing services for certain individuals.
Specifically, states may cover such services for individuals under the age of 21 (or a lower age, if the state chooses) and for former foster youth under the age of 26 who (1) have been referred or admitted to an intensive care unit or seen by a medical specialist for a suspected genetic or undiagnosed disease, or (2) are suspected by a medical specialist to have a neonatal- or pediatric-onset genetic disease.
The Centers for Medicare & Medicaid Services may award grants to assist states in developing plans to cover such services.
- Introduced in Senate Formatted Text PDF Formatted XML
Cite this page
U.S. Congress. (2026). S. 3116: Ending the Diagnostic Odyssey Act of 2019. 116th Congress. Open America. https://openamerica.io/bill/116-S-3116/
"S. 3116: Ending the Diagnostic Odyssey Act of 2019." 116th Congress, 2026, Open America, https://openamerica.io/bill/116-S-3116/.
S. 3116, 116th Cong. (2026), https://openamerica.io/bill/116-S-3116/.
[S. 3116: Ending the Diagnostic Odyssey Act of 2019](https://openamerica.io/bill/116-S-3116/)