• Birth Defects, Genetic Diseases Research

• 307.

Kate Foundation for Rett Syndrome Research Inc

The Kate Foundation is a 501(c)(3) organization dedicated to raising research funding for the reversal of Rett Syndrome and related disorders.

Down Syndrome Association Northwest Indiana

Our mission is to raise awareness, provide support, advocate for inclusion, and change as our population needs us to as a steadfast resource for the Down Syndrome community.

The Global Foundation for Peroxisomal Disorders

The GFPD's mission is to improve the lives of individuals with peroxisomal disorders by funding research, championing scientific collaboration, and empowering families and professionals through educational programs and support services.

• Human Service Organizations

• 310.

ChadTough Defeat DIPG Foundation

In the fight for a DIPG/DMG cure, we help patients and families by funding game-changing research and providing navigation throughout their journey.

• Specifically Named Diseases

• 311.

3Q29 Foundation

3q29 Foundation Creating a path to treatment for chromosome 3q29 syndromes through funding research communitybuilding and increasing access to information and resources.

Rarekc Foundation

Our mission is to drive innovation in the diagnosis, care and treatment of rare diseases by connecting and inspiring our community.

• Specifically Named Diseases

• 313.

Project CASK

An innovative rare disease non-profit driving breakthroughs in treatments and a cure for CASK gene disorders.

• Nerve, Muscle, and Bone Diseases

• 314.

Lynk Up World (LUW)

Lynk Up • World (LUW) is on a mission to bring meaningful connection to children & families impacted by rare diseases through art, support and innovation.

STAR CENTER INC

The STAR Center's mission is to help any person with any disability to realize their potential.