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.

Race for Adam Foundation

Adam Recke was diagnosed in 2005 with an extremely rare, degenerative terminal disease, Type-C Niemann-Pick Syndrome.

Phelan McDermid Syndrome Foundation

Official site of the Phelan-McDermid Syndrome Foundation.

• Birth Defects, Genetic Diseases

• 67.

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.

• Birth Defects, Genetic Diseases

• 68.

Uba5 Foundation

This page is to help raise awareness and connect with others that have been diagnosed UBA5 gene mutation.

Hunters CMT4B3 Research Foundation Inc

Pioneering cutting edge scientific research to develop treatments for CMT4B3 patients and children with rare neuromuscular diseases.

• Birth Defects, Genetic Diseases

• 70.

Irf2Bpl Foundation

Raising Awareness and Research Funds for IRF2BPLDisorder This website provides the information onIRF2BPLrelated disorders for patients family members physicians and biomedical scientists working all together to solve the medical mystery on IRF2BPL.

• Birth Defects, Genetic Diseases

• 71.

DADA2 Foundation

We're a nonprofit looking for innovative ways to accelerate research into the rare inflammatory disease DADA2.

• Group Home (Long-Term, Primarily Assisted Living)

• 72.

Prader-Willi Homes of California

PraderWilli Syndrome Center France ABOUT PWS PraderWilli Syndrome PWS is a complex rare and random genetic disorder that affects one in twelve to fifteen thousand people.