Similar organisations to The Shank2 Foundation
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Diseases, Disorders, Medical Disciplines N.E.C.
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28.
RASOPATHIES NETWORK USA
A 501c3 organization; Our mission is to advance research of the #RASopathies by bringing stakeholders together.
2552
Legal name of organization: RASOPATHIES NETWORK USA
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Epilepsy Research
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29.
Bridge the Gap
SYNGAP1 Foundation is a legacy page dedicated to preserving the work and mission of our 100% charitable nonprofit in the USA, focused on #SYNGAP1 To serve, educate and fund research for families coping with the effects of SYNGAP mutations.
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Cypress
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Specifically Named Diseases Research
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30.
GRACE SCIENCE FOUNDATION
We are changing how scientific research is done.
5373
Menlo Park
NEW HOPE RESEARCH FOUNDATION
The New Hope Research Foundation is a non-profit organization dedicated to: - Finding a genetic cure for GM2 gangliosidosis and other lysosomal storage diseases that affect the central nervous system, and - Providing hope to patients and their families currently facing the degenerative and debilitating aspects of these diseases.
North Oaks
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Birth Defects, Genetic Diseases Research
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32.
International FOXP1 Foundation
Our mission is to build a global community that empowers and supports families and individuals with FOXP1 syndrome by sharing knowledge, inspiring hope, supporting research, and raising awareness.
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Mendenhall
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Specifically Named Diseases
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33.
NR2F1 FOUNDATION
Empowering families and individuals living with rare #NR2F1 mutations through education, awareness and research.
2166
Royal Oak
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Specifically Named Diseases
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34.
YBRP Inc
YBRP is a non-profit organization whose mission is to positively impact the lives of individuals with HNRNPH2 genetic variations.
212
New Rochelle
CureLGMD2i Foundation
The CureLGMD2i Foundation strives to raise awareness and to support scientific research that is geared directly toward finding a treatment or cure for Limb Girdle Muscular Dystrophy type 2i (LGMD2i).
LANCASTER
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Fund Raising and/or Fund Distribution
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36.
THE YAYA FOUNDATION FOR 4H LEUKODYSTOPHY
Fighting for children and families affected by 4H Leukodystrophy.
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MINNEAPOLIS






