• Professional Societies & Associations

• 37.

Suneel Research Foundation

Our mission is to spread awareness about Duchenne Muscular Dystrophy (DMD), raise funds to support treatments and find a cure for DMD.

National MPS Society, Inc.

The National MPS Society exists to find cures for MPS and ML.

HSAN1E Society

Patient advocacy organization fighting for awareness and research of HSAN1E #RareDisease #Hearingloss #Neuropathy #Dementia #neurological disease HSAN1E Society’s purpose is to create awareness of HSAN1E, to provide emotional support to families affected by HSAN1E and help facilitate research.

• Alliance/Advocacy Organizations

• 40.

Hyper Igm Foundation

Our mission is to improve the treatment, quality of life and the long term outlook for children & adults living with Hyper IgM Syndrome Our mission to improve the treatment, quality of life and the long term outlook for children and adults living with Hyper IGM through research, support, education, and advocacy.

• Epilepsy

• 41.

Where Theres A Will Theres A Cure

We are going to cure X-Linked Myotubular Myopathy.

• Epilepsy

• 42.

Cure Ahc Foundation

Alternating Hemiplegia of Childhood (AHC) is a complex, ultra-rare neurological disease.

• Eye Diseases, Blindness & Vision Impairment

• 43.

BCM FAMILIES FOUNDATION

To eradicate Blue Cone Monochromacy (BCM), to provide financial support for research, projects, activities and organizations related to the diagnosis, treatment and/or cure of Blue Cone Monochromacy ("BCM"),to establish networks and synergies with other groups and organizations dedicated to eye and/or other rare disease issues, to make support and resources available to BCM patients and their involved families, and to educate the general public regarding BCM.

• Alliance/Advocacy Organizations

• 44.

Coffin-Siris Syndrome Foundation

Coffin-Siris Syndrome Foundation is a 501c3 that exists to connect, support, and inform those affected by Coffin-Siris Syndrome and related disorders and promote related research.

• Birth Defects, Genetic Diseases Research

• 45.

ADLD CENTER

The ADLD Center is focused on raising awareness about Autosomal Dominant Leukodystrophy ADLD and developing a network of clinicians researchers patients and their caregiversadvocates in order to raise funds as we move forward towards finding a cure.