• Specifically Named Diseases Research

• 496.

Juvenile Diabetes Research Foundation KC Chapter

As we drive toward curing type 1 diabetes, we help make everyday life better for the people who face it.

• Fund Raising and/or Fund Distribution

• 497.

Receptions for Research

Carolina’s family relief program for pediatric cardiovascular patients ❤️💚 The Foundation supports families of children with congenital heart disease with in-home nursing care and comprehensive medical services.

American Behcet's Disease Association (ABDA)

Bringing national focus, advocacy, research and awareness of Behcet's Disease Support.

NOTHING PINK INC

NothingPink is a Non-Profit Organization with an objective of achieving the following mission: To make genetic testing more accessible to women.

• Hospitals and Primary Medical Care Facilities

• 500.

Foundation for Mount Nittany Medical Center

Mount Nittany Health: A modern comprehensive healthcare system with 220 providers and 30+ specialties The Foundation for Mount Nittany Medical Center is dedicated to improving the quality of life for people of our region by supporting the advancement of healthcare at Mount Nittany Medical Center.

• Birth Defects, Genetic Diseases

• 501.

Irf2Bpl Foundation

Raising Awareness and Research Funds for IRF2BPLDisorder This website provides the information onIRF2BPLrelated disorders for patients family members physicians and biomedical scientists working all together to solve the medical mystery on IRF2BPL.

CANAVAN RESEARCH ILLINOIS

Join the worldwide mission to cure Canavan disease.

• Birth Defects, Genetic Diseases

• 503.

BPAN WARRIORS

Community resources, research and CONNECTION for BPAN Warrior families (WDR45, NBIA, Rare Disease, Parkinsons, Dementia, Epilepsy, Neurodegeneration, Genetics) BPAN Warriors is a growing international community of individuals who have loved ones directly affec BPAN WARRIORS CONNECT COLLABORATE CURE HOME RESEARCH PATIENT RESOURCES OUR TRIBE OUR PARTNERS DONATE RARE POV BLOG More 414 909BPAN RAREX unveils plan to radically change data collection and sharing to accelerate advances for patients in rare disease How One Rare Disease Advocate Learned to Look Across Diseases Study Makes Economic Case for Benefits of Data Sharing to Improve Diagnosis and Treatment of Rare Disease Patients Harnessing Machine Learning to Improve Diagnosis and Treatment of Rare Diseases Making Collaboration the Rule Rather than the Exception Why Data Sharing Is Critical for Accelerating Progress in Rare Disease PatientPowered Registry Boosts the Study of a Rare Disease What is Data Governance.

• Organ and Tissue Bank

• 504.

SUMMIT FOR STEM CELL FOUNDATION

Summit is a 501(c)(3), charitable organization working towards a victory over Parkinson’s About Summit Donate NOW Our mission Summit for Stem Cell Foundations mission is to support educate and raise awareness about the development of todays and tomorrows evidencebased regenerative medical therapies focused on Stem Cells 101 Donate Today Download Document What are Stem Cells.