Registry Report 2014

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Pages in this Report
  1. Highlights & Acknowledgements
  2. Background
  3. Methods
  4. Geographic Distribution of Registry Participants
  5. Registry Characteristics 2014
  6. Diagnosis
  7. Sex
  8. Age
  9. Race/Ethnicity
  10. Education
  11. Weight Status
  12. Health Insurance Coverage
  13. Health Insurance Coverage by Age
  14. Viral and Vaccination Status
  15. Use of Healthcare Services and Absenteeism
  16. Chronic Diseases, Conditions, or Surgical Procedures
  17. Technical Notes
  18. Participating HTCs
Diverse groupd of young adults.

The Division of Blood Disorders, National Center on Birth Defects and Development Disabilities, and the Centers for Disease Control and Prevention (CDC) in Atlanta, Georgia published the 2014 Community Counts Registry Report.

All data are provisional.

Suggested Citation: Centers for Disease Control and Prevention. 2014 Community Counts Registry Report. https://www.cdc.gov/ncbddd/hemophilia/communitycounts/registry-report/index.html. Published August 2018. Accessed [date].

The Division of Blood Disorders, National Center on Birth Defects and Development Disabilities, and the Centers for Disease Control and Prevention (CDC) in Atlanta, Georgia published the 2014 Community Counts Registry Report. This report was prepared by the following CDC staff: Karon Abe, Brandi Dupervil, Vanessa Byams, Binh Le, Mais Aboneaaj, Meredith Oakley, and J. Michael Soucie.

Highlights & Acknowledgements