• Birth Defects, Genetic Diseases

• 316.

Cystic Fibrosis Awareness Foundation A New Jersey Nonprofit

The mission of the CFAF is to increase public awareness of Cystic Fibrosis.

• Alliance/Advocacy Organizations

• 317.

The Charles E. Holman Morgellons Disease Foundation

The Charles E. Holman Foundation is a #grassroots organization that supports research, education, diagnosis and treatment of #Morgellons Disease.

• Nerve, Muscle, and Bone Research

• 318.

Joshuas Future of Promises Inc

Joshua’s Future Of Promises is a non-profit organization set up by Joshua Scoble’s family.

• Nerve, Muscle, and Bone Diseases

• 319.

Cohen Syndrome Association

Welcome to the Official fan page of the Cohen Syndrome Association ®.

• Organ and Tissue Bank

• 320.

Kidney Champion Foundation

The Kidney Champion Foundation educates historically marginalized and underserved communities about kidney disease while fighting for inclusive and equitable access to care.

• Nonmonetary Support N.E.C.*

• 321.

N 1 Collaborative Inc

OUR MISSION IS TO MAKE INDIVIDUALIZED MEDICINES ROUTINELY AND RAPIDLY ACCESSIBLE TO RARE DISEASE PATIENTS WORLDWIDE.

• Birth Defects, Genetic Diseases

• 322.

Kinslow Tubb4a Foundation Inc

Our mission is to provide information on accessible and equitable treatment options for every child affected by TUBB4A-related leukodystrophy, regardless of their geographical location or socioeconomic status.

Rarekc Foundation

Our mission is to drive innovation in the diagnosis, care and treatment of rare diseases by connecting and inspiring our community.

• Health Support Services

• 324.

ConnectMyVariant

Prevention through Connection An innovative nonprofit that builds communities dedicated to communication with relatives about genetic testing and hereditary disease prevention Get free help reaching out to relatives and find a community of others who have your variant.