The Global Foundation for Peroxisomal Disorders

The GFPD's mission is to improve the lives of individuals with peroxisomal disorders by funding research, championing scientific collaboration, and empowering families and professionals through educational programs and support services.

• Birth Defects, Genetic Diseases

• 38.

Cystic Fibrosis Foundation

Recognized globally, the CF Foundation has led the way in the fight against cystic fibrosis, fueling extraordinary medical and scientific progress.

• Specifically Named Diseases

• 39.

CADASIL Association

cureCADASIL is a non-profit organization committed to curing #CADASIL and improving the quality of life for those affected by this genetic disease.

• Fund Raising and/or Fund Distribution

• 40.

Curears A NJ Nonprofit Corporation

Our mission is to spread awareness, connect and provide support to affected families and fund research for the ultra-rare mtARS genes.

• Specifically Named Diseases

• 41.

Abetalipoproteinemia and Related Disorders Foundation

Abetalipoproteinemia and Related Disorders Foundation is a non-profit, volunteer organization that provides guidance on needed scientific research, diagnosis, and management of abetalipoproteinemia and related hypolipidemias.

• Cancer

• 42.

Fbxo31 Foundation

The FBXO31 Foundation was formed to eradicate FBXO31-related cerebral palsy by raising awareness and funds to accelerate research for a cure.

• Fund Raising and/or Fund Distribution

• 43.

Tough Genes Inc

Currently, there is no treatment for IRF2BPL-Related Disorder.

• Fund Raising and/or Fund Distribution

• 44.

HOPE FOR HARVEY FOUNDATION INC

Register for the 4th Annual Hope for Harvey Golf Tournament on 882025.

• Fund Raising and/or Fund Distribution

• 45.

GLUT1 DEFICIENCY FOUNDATION INC

Building a brighter future Bringing help and hope to the Glut1 Deficiency community as we work together to improve lives through awareness education advocacy and research Shining a light on Glut1 Deficiency Glucose Transporter Protein Type 1 Deficiency Syndrome Glut1 Deficiency is a rare genetic condition that impairs brain metabolism.