Similar organisations to NOONAN SYNDROME FOUNDATION
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Family Services
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73.
National Foundation for Autism Research (NFAR)
NFAR is dedicated to building a more inclusive future for those with autism.
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San Diego
Race for Adam Foundation
Adam Recke was diagnosed in 2005 with an extremely rare, degenerative terminal disease, Type-C Niemann-Pick Syndrome.
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Emmaus
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Birth Defects, Genetic Diseases Research
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75.
SMS Research Foundation
The mission of the Smith-Magenis Syndrome Research Foundation is to advance scientific research leading to innovative treatment options for people living with SMS.
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Patient Services�Entertainment, Recreation
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76.
OMSLIFE FOUNDATION INC
For research and awareness of rare deseases Home Our mission is to raise awareness of Opsoclonus Myoclonus Syndrome maintain a support network for caregivers and fund research for a cure.
Cypress
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Private Grantmaking Foundations
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77.
Wallace Beeson Foundation Inc
A 501(c) founded in 2017 to raise money for research in rare Neurogastrointestinal & Motility Disease Home About Research Our Team More JOIN OUR FIGHT TOMAKE RARE KNOWN Funding Research for Rare Neurogastrointestinal Motility disorders YOUR DONATION FUNDS A DESPERATE NEED IN RESEARCH HOW WE STARTED From being a healthy 15yearold competitive swimmer to having to fight for herlife almost overnight Wallacesaw first hand the effect a rare condition has on someone.
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Zttk Son-Shine Foundation Inc
Welcome to the Official Website of the ZTTK SONShine Foundation.
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Public Foundations
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79.
The Mathew Forbes Romer Foundation Inc
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Boca Raton
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Birth Defects, Genetic Diseases
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80.
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.
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Houston
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Fund Raising and/or Fund Distribution
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81.
BFLS Incorporated
Mom on a mission to raise awareness and funds for research for the rare genetic disorder Börjeson-Forssman-Lehman Syndrome or BFLS� Born Fierce.
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Bakersfield




