• Biomedicine, Bioengineering

• 91.

National Biomedical Research Ethics Council

Item 1 NBREC was to estabish a single.

• Diseases, Disorders, Medical Disciplines N.E.C.

• 92.

National Niemann-Pick Disease Foundation

National Niemann-Pick Disease Foundation The NNPDF offers support and guidance to families and patients of those affected by Niemann-Pick Dise Mission: We are a non-profit group dedicated to supporting and empowering patients and families affected by Niemann-Pick disease through education, collaboration and research.

• Fund Raising and/or Fund Distribution

• 93.

Eleanor Kaplan Foundation Inc

To raise funds and awareness to develop cures for Ultra Rare Neurodegenerative Diseases.

• Alliance/Advocacy Organizations

• 94.

Finding Nori Foundation

The Finding Nori Foundation Home About Meet the Team Finding Joy Blog Resources Publications DONATE Contact Upcoming Events More Raising research funding for PAX5 and ALG13 related neurological disordersEmpowering families with ultra rare undiagnosed diseases to find answers Our Mission Our mission is to advance scientific research through fundraising and advocacy for ultra rare undiagnosed genetic disorders.

• Birth Defects, Genetic Diseases

• 95.

Mitchell and Friends Foundation

To raise awareness of Mitchell Syndrome and support research into possible treatments and cures Raising awareness of Mitchell Syndrome and supporting families and children with this rare neurological disease.

• Mental Health Disorders

• 96.

Lauren Marie Levert Foundation To Cure Schizophrenia Inc

THE LAUREN MARIE LEVERT FOUNDATION IS DEDICATED TO FUNDING THE RESEARCH AND CURE FOR SCHIZOPHRENIA.

CANAVAN RESEARCH ILLINOIS

Join the worldwide mission to cure Canavan disease.

• Fund Raising and/or Fund Distribution

• 98.

HOPE FOR HARVEY FOUNDATION INC

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

• Birth Defects, Genetic Diseases

• 99.

GRIN2B FOUNDATION

Our goal is to offer support and share research to the small, but growing community of children diagnosed with alterations on their GRIN2B gene.