• Birth Defects, Genetic Diseases

• 91.

The Sickle Cell Cure Foundation Inc

Sorry this product is unavailable. Please choose a different combination.

• Hospital (Specialty)

• 92.

Translational Pulmonary and Immunology Research Center

TPIRC is a rare disease institute focused on 6 orphan conditions: Food Allergies, Cystic Fibrosis, Br TPIRC IS A NON-PROFIT CLINICAL CARE AND RESEARCH CENTER THAT FOCUSES ON THE DEVELOPMENT OF CUTTING-EDGE, INDIVIDUALIZED TREATMENT PROTOCOLS FOR RARE AND ORPHAN DISEASES UTILIZING COMPREHENSIVE DIAGNOSTIC TOOLS AND PATIENT DRIVEN RESEARCH.

• Research Institutes and/or Public Policy Analysis

• 93.

Rare Science

We are a nonprofit research organization accelerating therapeutic solutions for patients and fostering research collaboration in the rare disease community.

Foxg1 Research Foundation

FOXG1 syndrome is a childhood neurological genetic disorder and is a key to understanding many brain disorders.

• Birth Defects, Genetic Diseases Research

• 95.

Spata Foundation Inc

Our mission is to advocate, educate, and raise funds for research towards SPATA5 & SPATA5L1 Disorders The SPATA Foundation's Mission is to advocate, educate, and drive research towards SPATA5 and SPATA5L1 Related Disorders.

• Alliance/Advocacy Organizations

• 96.

Advocates for Universal Dpd-Dpyd Testing

Advocating for pre-testing for DPD Deficiency prior to treatment with fluorouracil-based chemotherapy: 5-FU or Xeloda(capecitabine) to improve the standard of care for cancer patients and save lives.

Upequity Corporation

RareRising, is a 501c3 that delivers research, incubates emerging rare disease entities, and explores solutions to positively impact rare disease communities.

• Birth Defects, Genetic Diseases

• 98.

EBF3 HADDS Foundation

EBF3 HADDS FOUNDATION Home SupportDonate About Events Blog Shop More ARTICLES EVENTS BLOG CONNECT Learn more about what is happening globally with our community.

• Fund Raising and/or Fund Distribution

• 99.

NORTH CAROLINA RARE DISEASE

Rare Disease Innovations Institute Our Mission RDII is a global nonprofit focused on educating engaging and equipping the rare disease community.