Registry Report on Males With Hemophilia 2014-2017

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Pages in this Report
  1. Highlights & Acknowledgements
  2. Background
  3. Methods
  4. Geographic Distribution of Registry Participants
  5. Diagnosis & Severity
  6. Registry Characteristics
  7. Age
  8. Race/Ethnicity
  9. Education
  10. Weight Status
  11. Health Insurance Coverage
  12. Viral and Vaccination Status
  13. Healthcare Utilization and Absenteeism
  14. Family History and Genetic Mutation
  15. Complications
  16. Treatment
  17. Procedures and Comorbid Conditions
  18. Technical Notes
  19. Participating HTCs

The Community Counts Registry Report – Males with Hemophilia 2014–2017 – is published by the Division of Blood Disorders (DBD), National Center on Birth Defects and Developmental Disabilities (NCBDDD), Centers for Disease Control and Prevention (CDC), Atlanta, Georgia 30341.

All data are provisional.

Suggested Citation: Centers for Disease Control and Prevention. Community Counts Registry Report – Males with Hemophilia 2014–2017, Month year:X-XX

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: Brandi Dupervil, Binh Le, Vanessa Byams, Karon Abe, Meredith Oakley, J. Michael Soucie, and Laura Schieve.

Highlights & Acknowledgements