• Education N.E.C.

• 154.

Spinal Muscular Atrophy Foundation

The mission of the Spinal Muscular Atrophy Foundation is to accelerate the development of a treatment for SMA, the number one genetic killer of infants and toddlers.

THE CLINIC FOR SPECIAL CHILDREN INC

A nonprofit comprehensive medical practice focused on treating & researching rare genetic disorders.

• Nerve, Muscle, and Bone Research

• 156.

Lgmd2L Foundation

We’re a nonprofit searching for a cure for LGMD2L, a rare disease that causes muscle weakness and atrophy, pain, and eventually leads to many sufferers being unable to walk.

LIV4THECURE

Liv4TheCure’s mission is to promote awareness, help families and fund research for Wolf Hirschhorn Syndrome.

Ellie Ruby Foundation Inc

Our mission is to bring smiles and support to families battling pediatric cancer Our mission is to bring smiles and support to families battling pediatric cancer.

• Birth Defects, Genetic Diseases

• 159.

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

• 160.

The PolG Foundation

The mission of The POLG Foundation is to support and accelerate research to find effective treatments and a cure for PolG mitochondrial disorders.

• Birth Defects, Genetic Diseases Research

• 161.

Luca Gargiulo Pearson Foundation Inc

The Luca Gargiulo Pearson Foundation will support and offer financial research and development to help find a cure for Pearson Syndrome.

• Science & Technology Research Institutes, Services N.E.C.

• 162.

HUDSON-ALPHA INSTITUTE FOR

A nonprofit institute where scientists, educators, clinicians and entrepreneurs collaborate and apply genomics to improve the human condition around the globe.