• Professional Societies & Associations

• 55.

American Society for Nutrition Inc

ASN advances the science, education and practice of nutrition through knowledge, engagement & impact @JNutritionOrg @AJCNutrition #Nutrition2025 A Healthier World Through Evidence-Based Nutrition TO IMPROVE HEALTH AROUND THE WORLD THROUGH EVIDENCE-BASED NUTRITION BY ADVANCING THE SCIENCE, EDUCATION, AND PRACTICE OF NUTRITION.

• Specifically Named Diseases

• 56.

Pituitary World News

Pituitary World News was established in 2014 to increase awareness of pituitary disease so more people are diagnosed properly and early.

• Birth Defects, Genetic Diseases

• 57.

Curefa Foundation Inc

CUREFA FOUNDATION FUNDS CAPITAL INTENSIVE PROJECTS GATED WITH SUCCESS MILESTONES, LEVERAGING NOVEL TOOLS OF SCIENTIFIC RESEARCH FOR THE TREATMENT AND CURE OF FRIEDREICH'S ATAXIA.

• Specifically Named Diseases

• 58.

Wylder Nation Foundation

WARRIORS in the Fight Against Lysosomal Storage Disorders.

ALD Alliance

Fighting to pass Aidan's Law for National Newborn Screening for all RUSP conditions.

• Birth Defects, Genetic Diseases Research

• 60.

International Association for Chronic Fatigue Syndrome-Me

THE MISSION OF IACFS/ME IS TO PROMOTE, STIMULATE AND COORDINATE THE EXCHANGE OF IDEAS RELATED TO CHRONIC FATIGUE SYNDRONE(CFS) AND FIBROMYALGIA(FM) RESEARCH, PATIENT CARE AND TREATMENT IN ADDITION, THE IACFS/ME PERIODICALLY REVIEWS THE CURRENT RESEARCH AND TREATMENT LITERATURE AND MEDIA REPORTS FOR THE BENEFIT OF SCIENTISTS, CLINICIANS AND PATIENTS.

• Fund Raising and/or Fund Distribution

• 61.

Diet Detective Inc

The Center for Food As Medicine & Longevity is a nonprofit organization that works to uncover the mysteries and myths surrounding food, nutrition, and medicine.

Dlg4 Research Fund

DLG4-related Synaptopathy / SHINE Syndrome *Managed by the board of the DLG4 SHINE Foundation A page for people interested in learning more about DLG4-related Synaptopathy / SHINE Syndrome *Managed by the board of the DLG4 SHINE Foundation Mission To find specific treatment options and a cure for DLG4 patients by building a collaborative network of patients, families, clinicians and scientists that will work together to raise awareness and accelerate the understanding, diagnosis and treatment of DLG4 related synaptopathy.

• Birth Defects, Genetic Diseases Research

• 63.

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.