Hereditary Disease Foundation

The official Twitter feed of the Hereditary Disease Foundation.

• Other Philanthropy, Voluntarism, and Grantmaking Foundations N.E.C.

• 38.

Proteus Syndrome Foundation

The Proteus Syndrome Foundation, a 501c3 not-for-profit organization, is dedicated improving the lives of Proteus patients by funding AKT1 research.

• Birth Defects, Genetic Diseases

• 39.

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.

• Health Support Services

• 40.

Pharmaceutical Research and Manufacturers of America Fnd Inc

The PhRMA Foundation supports early-career researchers by awarding them competitive fellowships and grants.

• Health Support Services

• 41.

Pyruvate Kinase Deficiency Foundation

The Pyruvate Kinase Deficiency International Alliance is an international nonprofit organization whose mission is to enhance the quality of life for patients and their families by providing awareness, expanding education, and promoting advocacy.

• Fund Raising and/or Fund Distribution

• 42.

Alexander's Way Research Fund Inc

We promote the development of a treatment or cure for the rare genetic disease known as myofibrillar myopathy 6, (MFM6).

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.

• Fund Raising and/or Fund Distribution

• 44.

Ara Parseghian Medical Research Foundation

The Ara Parseghian Medical Research Foundation (APMRF) was founded in 1994.

International Rett Syndrome Foundation

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.