GALACTOSEMIA FOUNDATION

A national, nonprofit, volunteer organization providing information, support and networking opportunities to those impacted by galactosemia since 1985 Galactosemia Foundation is a national, non-profit, volunteer organization whose mission is to provide information, support, and networking opportunities to families affected by galactosemia.

Hereditary Disease Foundation

The official Twitter feed of the Hereditary Disease Foundation.

• Birth Defects, Genetic Diseases Research

• 102.

Fam177a1 Research Fund

Founder and President, FAM177A1 Research Fund The mission of the FAM177A1 Research Fund is to improve the lives of those affected by FAM177A1 Associated Disorder through research and development of transformative therapies.

COPA Syndrome Foundation

The COPA syndrome is an inherited disorder that is caused by mutations in the COPA gene.

• Nonmonetary Support N.E.C.*

• 104.

Curedrpla Inc

I’m a parent advocate for DRPLA, a rare genetic disease.

Malan Syndrome Foundation Inc

Malan syndrome is a rare genetic disorder that is the result of a change in the NFIX gene.

Lcc Foundation Inc

The LCC Foundation’s MISSION is to help families across the United States and beyond diagnosed with Leukoencephalopathy with Brain Calcifications and Cysts (LCC) by giving them the resources they need to fight this rare and devastating disease.

• Services to Promote the Independence of Specific Populations

• 107.

Myasthenia Gravis Foundation of California

To find a cure for Myasthenia Gravis by funding cutting edge research and providing services for Myasthenia Gravis patients, as well as medical education, information and referrals.

• Fund Raising and/or Fund Distribution

• 108.

Tango2 Research Foundation Incorporated

Our mission is to lead the way in finding a cure for TANGO2 related disease.