• Birth Defects, Genetic Diseases Research

• 91.

NEW YORK STEM CELL FOUNDATION INC

The NYSCF Research Institute is a non-profit organization whose mission is to cure the major diseases of our time through stem cell research.

• Fund-Raising Organizations that Cross Categories (includes Community Funds/Trusts and Federated Giving Programs) e.g. United Way

• 92.

Marcum Foundation Inc

Our mission is to support causes that focus on improving the health and wellbeing of children.

• Diseases, Disorders, Medical Disciplines N.E.C.

• 93.

LYMPHANGIOMATOSIS & GORHAMS DISEASE ALLIANCE INC

Patient-driven solutions for complex lymphatic anomalies: GLA, GSD, KLA, CCLA • Support-Research-Education • Somatic mutations PIK3/mTor & RAS/MAPK pathways Patient advocacy group dedicated to patient driven solutions for complex lymphatic anomalies We connect patients and families to peers and networks of care, partner to advance new research, and educate the medical community to help all people navigating complex lymphatic anomalies have hope for a healthier tomorrow.

Rheumatology Research Foundation

Advancing research and training to improve the health of people with rheumatic diseases.

The Evelyn Swierczynski Foundation

The Evelyn Swierczynski Foundation’s mission is to support CHLA through fundraising events and events like our annual holiday book drive and bi-annual blood/bone marrow drives.

• Birth Defects, Genetic Diseases Research

• 96.

Rory Belle Foundation

We are a family run foundation established to raise funding and awareness for a gene therapy cure for the NARS1 disease.

CMT Research Foundation Inc

The CMT Research Foundation has one mission: Deliver treatments and cures for #CMT.

SICKLE CELL DISEASE FOUNDATION

Providing education and life-enhancing programs to individuals with sickle cell disease.

• Alliance/Advocacy Organizations

• 99.

Ctx Alliance NFP

Providing education, support, advocacy, and promoting research for CTX patients, their families, and medical professionals who treat and study this rare disease Providing education, support, advocacy, and promoting research for CTX patients, their families, and medical professionals who treat and study this rare disease.