APBD RESEARCH FOUNDATION

Supporting individuals and families affected by Adult Polyglucosan Body Disease (APBD), and accelerating improved APBD diagnoses, care and treatment options.

• Fund Raising and/or Fund Distribution

• 92.

Forest Hills Educational Foundation

The European Network of Patient Organizations for inherited lipid conditions #FindFH #FindHoFH #FindLpa #FindFCS Working together to provide a stronger future for individuals and families with FH and other forms of inherited/genetic dislipidemias.

• Public, Society Benefit - Multipurpose & Other N.E.C.

• 93.

CheckOrphan

CheckOrphan is the leading source for news and information about rare diseases.

• Professional Societies & Associations

• 94.

Gout Hyperuricemia and Crystal-Associated Disease Network

LAUNCH AND SUPPORT NOVEL RESEARCH AND EDUCATION INITIATIVES TO HELP FILL THE KNOWLEDGE GAP IN THE PATHOGENESIS, DIAGNOSIS, TREATMENT, AND OUTCOMES OF GOUT, HYPERURICEMIA, AND CRYSTAL DEPOSITION-ASSOCIATED DISORDERS (INCLUDING CARDIOVASCULAR DISEASES); FACILITATE THE SHARING OF RESOURCES AND INFORMATION RELATED TO GOUT, HYPERURICEMIA, AND CRYSTAL-ASSOCIATED DISEASES; AND FOSTER NETWORKING AND COLLABORATION ACROSS RELATED MEDICAL DISCIPLINES AND SCIENTIFIC COMMUNITIES THAT CARE FOR AND STUDY THESE CONDITIONS.

Cure KCNH1 Foundation

Cure KCNH1 Foundation is dedicated to advancing the development of treatments for children with KCNH1 genetic disorders.

• Birth Defects, Genetic Diseases

• 96.

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.

• Fund Raising and/or Fund Distribution

• 97.

Alexander's Way Research Fund Inc

We promote the development of a treatment or cure for the rare genetic disease known as myofibrillar myopathy 6, (MFM6).

United MSD Foundation

Our mission is simple, yet powerful: To cure Multiple Sulfatase Deficiency.

• Medical Specialty Research

• 99.

Curemapk8Ip3 Foundation

Family support network for patients and their families affected by a gene mutation in MAPK8IP3 Page for individuals and families with gene variant MAPK8IP3 Improve the lives of patients and families affected by a MAPK8IP3 gene mutation by performing the following activities: raising community awareness of MAPK8IP3-Related Neurodevelopmental Disorder; facilitating research of MAPK8IP3-Related Neurodevelopmental and related Disorders; collecting and disseminating information and resources relating to MAPK8IP3-Related Neurodevelopmental and related Disorders; supporting those affected by MAPK8IP3-Related Neurodevelopmental and related Disorders; and any other charitable educational or scientific activities that are in furtherance of the Corporation's purposes.