• Museums & Museum Activities

• 118.

Prader Willi Association of New England Inc

PWS is a non-inherited genetic disorder which is associated with a random deletion of the 15th chromosome.

• Birth Defects, Genetic Diseases Research

• 119.

Hope for Pdcd Foundation

Fundraising for a cure for Pyruvate Dehydrogenase Complex Deficiency (PDCD) & advancing research for rare diseases.

• Birth Defects, Genetic Diseases Research

• 120.

Spata Foundation Inc

Our mission is to advocate, educate, and raise funds for research towards SPATA5 & SPATA5L1 Disorders The SPATA Foundation's Mission is to advocate, educate, and drive research towards SPATA5 and SPATA5L1 Related Disorders.

• Alliance/Advocacy Organizations

• 121.

The Shank2 Foundation

To improve the quality of life for individuals affected by SHANK2 disorders.

Willstrong Foundation Trust

WillStrong is dedicated to providing financial support for research to bring more precise and effective treatments to children and young adults diagnosed with acute myeloid and other high-risk leukemia.

• Health - General & Rehabilitative N.E.C.

• 123.

4P-Support Group

Our mission is to serve our membership by providing information, education and support; uniting families, researchers, and professionals; and promoting awareness and understanding of 4p- syndrome, with Wolf-Hirschhorn Syndrome as the main condition, and the related 4th chromosome abnormalities.

• Fund Raising and/or Fund Distribution

• 124.

The Children's Rare Disorders Fund

Dedicated to curing rare genetic disorders Founded in July 2022 by parents of a toddler affected by FOXG1, The CRD Fund focuses on under served communities in the rare disorder space.

• Patient Services�Entertainment, Recreation

• 125.

SCID Foundation

Disease awareness, support, education, and support of research for Severe Combined Immune Deficiency (SCID) The SCID Foundation is committed to increasing awareness, providing a safe environment for families to connect, advocating for the common concerns voiced by SCID patients or their families, and providing parent and family education for those affected by Severe Combined Immune Deficiency.

• Cancer

• 126.

CHILDREN'S NEUROBLASTOMA CANCER

The Children’s Neuroblastoma Cancer Foundation (CNCF) is the premier source for neuroblastoma information and resources.