• Cultural/Ethnic Awareness

• 361.

National Phillipine Cultural Foundation Inc

The National Pediatric Cancer Foundation is dedicated to research and clinical trials to find less toxic, more effective treatments for #pediatriccancer NPCF is a nonprofit organization dedicated to research and clinical trials to treat pediatric cancer.

• Alliance/Advocacy Organizations

• 362.

PTEN Hamartoma Tumor Syndrome Foundation

PTEN is a tumor suppressor gene. When mutated at birth a patient is at higher risk for many #cancers and #autism.

• Birth Defects, Genetic Diseases

• 363.

Xeroderma Pigmentosum Family Support Group

The XP Family Support Group is dedicated to improving the quality of life of those with xeroderma pigmentosum.

USHER 1F COLLABORATIVE INC

Founded in December 2013, Usher 1F Collaborative is a 501c3 nonprofit foundation whose mission is to fund medical research to find an effective treatment to save or restore the vision of those with Usher Syndrome type 1F.

• Family Violence Shelters and Services

• 365.

New Beginnings Life Center Services NFP

FROM SURVIVING TO THRIVING. FROM SURVIVING TO THRIVING.

• Fund Raising and/or Fund Distribution

• 366.

Arid1B Research Foundation

Accelerating the development of disease-modifying treatments for #ARID1B-RD (haploinsufficiency) - the most frequently mutated gene in de novo NDDs (ASD, ID).

United MSD Foundation

Our mission is simple, yet powerful: To cure Multiple Sulfatase Deficiency.

• Human Service Organizations

• 368.

Chd Tablet Talk Foundation

CHD TABLET TALK FOUNDATION® A 501c3 Nonprofit Organization Keeping children with complex congenital heart disease (CHD) connected and engaged by providing resources, education, support, and mentorship 💙❤️ © 2020 All rights reserved The CHD Tablet Talk mission is to keep children with complex CHD, who are experiencing lengthy hospital stays, connected and engaged while they battle their illness.

• Brain Disorders

• 369.

THE PIERCE FAMILY FRAGILE X FOUNDATION

The Pierce Family Fragile X Foundation is a non-profit created to fund research, development of treatments, and community awareness to find a cure for Fragile X Created to fund dedicated research, development of treatments, and community awareness for Fragile X The Pierce Family Fragile X Foundation is a nonprofit organization that has been created to fund dedicated research development of treatments and community awareness in support of finding a cure for Fragile X Syndrome affecting our beautiful boys Graham and Reid.