Similar organisations to International FOXP1 Foundation
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Specifically Named Diseases Research
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46.
The Snow Foundation
A voice for rare disease, working towards a cure for Wolfram syndrome and developing novel therapies for diabetes, vision loss, hearing loss neurodegeneration.
3152
Clayton
Alpha-1 Foundation, Inc.
Our mission is to increase awareness of and find a cure for Alpha-1 Antitrypsin Deficiency.
24001
Coral Gables
Prader-Willi Syndrome Association | USA
What’s YOUR story. Tweet us and tell us what it’s like #GrowingUpRare We hope you will suggest the PWSA | USA facebook page to your friends.
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Legal name of organization: Prader-Willi Syndrome Association | USA
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Diseases, Disorders, Medical Disciplines N.E.C.
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49.
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.
1482
Fort Atkinson
Who Is Carter Foundation Inc
Nonprofit supporting families of children with brain injury and other neurological conditions July The conversation around brain injury--whether among physicians, families, communities, or society as a whole--is often limiting.
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KANSAS CITY
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Autism
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51.
FRAGILE X ASSOCIATION OF WASHINGTON STATE
News and information from the National Fragile X Foundation about Fragile X syndrome, FXTAS, FXPOI and the other Fragile X-associated disorders To be a resource to parents and families affected by Fragile X.
2714
Olympia
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Health - General & Rehabilitative N.E.C.
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52.
4P-Support Group
Our mission is to serve our membership by providing information, education and support; uniting families, researchers, and professionals; and promoting awareness and understanding of 4p- syndrome, with Wolf-Hirschhorn Syndrome as the main condition, and the related 4th chromosome abnormalities.
Livingston
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Birth Defects, Genetic Diseases
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53.
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.
547
Houston
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Specifically Named Diseases Research
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54.
THE FOCUS FOUNDATION INC
OUR FOCUS:Helping children who have* X & Y Variations* Dyslexia * DyspraxiaEarly Identification + Tar Early Awareness Detection Treatment for X Y Chromosomal Variation Disorders X Y Chromosomal Disorders 47 XXY 47 XYY 47 XXX Learn more about them.
1754
DAVIDSONVILLE






