• Digestive Diseases/Disorders Research

• 226.

Pediatric Digestion & Motility Disorders SOC Inc

Pediatric Digestion & Motility Disorders Society, Inc.

• Nerve, Muscle, and Bone Diseases

• 227.

Myasthenia Gravis Foundation of America, Inc.

#MyastheniaGravis Foundation of America (MGFA) is the largest nonprofit patient advocacy organization dedicated solely to improving the lives of people with MG.

• Birth Defects, Genetic Diseases

• 228.

International Rett Syndrome Association, Inc.

We are transforming lives every day in our fight to treat and cure Rett syndrome and better the lives of families living with this devastating disorder.

• Alliance/Advocacy Organizations

• 229.

Lipedema Project Inc

The Lipedema Project increases awareness and provides education, research and treatment for lipedema.

• Health (General and Financing)

• 230.

Little Zebra Fund

Universal access to clinical genetic testing.

• Professional Societies & Associations

• 231.

Hypertrophic Cardiomyopathy Medical Society

A community of physicians, scientists and medical providers dedicated to improving the diagnosis and treatment of hypertrophic cardiomyopathy Professional medical society dedicated to improving the diagnosis and treatment of people with hypertrophic cardiomyopathy through clinical excellence, research and education.

Dlg4 Research Fund

DLG4-related Synaptopathy / SHINE Syndrome *Managed by the board of the DLG4 SHINE Foundation A page for people interested in learning more about DLG4-related Synaptopathy / SHINE Syndrome *Managed by the board of the DLG4 SHINE Foundation Mission To find specific treatment options and a cure for DLG4 patients by building a collaborative network of patients, families, clinicians and scientists that will work together to raise awareness and accelerate the understanding, diagnosis and treatment of DLG4 related synaptopathy.

• Philanthropy/Charity/ Voluntarism Promotion (General)

• 233.

RARE IS BEAUTIFUL

In honor of Dee Dee Ingui, to find a cure for Peutz Jeghers Syndrome, which is a rare genetic disease.

• Fund Raising and/or Fund Distribution

• 234.

THE CHAMP FOUNDATION

Mission The Champ Foundation supports research toward better treatment and a cure for single largescale mitochondrial deletion syndromes SLSMDS like Pearson syndrome.