Similar organisations to International FOXP1 Foundation
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Fund Raising and/or Fund Distribution
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28.
Tbc1D24 Foundation
Tbc1d24 foundation is a research organization and connecting site for caregivers, families, and those diagnosed with Tbc1d24 mutations.
1600
Shohola
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Alliance/Advocacy Organizations
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29.
Jansen De Vries Syndrome Foundation
The Jansen de Vries Syndrome (JdVS) Foundation is a nonprofit, tax-exempt organization as defined in section 501(c)(3) of the Internal Revenue Code and, as such, contributions to JdVS Foundation are tax-deductible.
Natick
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Alliance/Advocacy Organizations
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30.
Nrxn1 Network
Our mission is to build a collaborative network of families, clinicians, and scientists in order to support individuals affected by NRXN1 disorder.
18
Lewisburg
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Specifically Named Diseases
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31.
Sisters Hope Foundation for Hereditary Diffuse Leukoencephalop
We are dedicated to amplifying patient voices, and one day meeting the first survivor of ALSP.
915
Myerstown
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Medical Specialty Research
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32.
Curemapk8Ip3 Foundation
Family support network for patients and their families affected by a gene mutation in MAPK8IP3 Page for individuals and families with gene variant MAPK8IP3 Improve the lives of patients and families affected by a MAPK8IP3 gene mutation by performing the following activities: raising community awareness of MAPK8IP3-Related Neurodevelopmental Disorder; facilitating research of MAPK8IP3-Related Neurodevelopmental and related Disorders; collecting and disseminating information and resources relating to MAPK8IP3-Related Neurodevelopmental and related Disorders; supporting those affected by MAPK8IP3-Related Neurodevelopmental and related Disorders; and any other charitable educational or scientific activities that are in furtherance of the Corporation's purposes.
85
Fort Mill
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Nonmonetary Support N.E.C.*
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33.
Global Neuro Ycare Inc
The mission of Global Neuro YCare is to educate through the creation and translation of materials and programs for children, youth and families; advocate with national and international organizations to guide the creation of regional, cultural and country specific programming; and support research addressing the needs and experiences of young carers.
Milwaukee
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Alliance/Advocacy Organizations
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34.
Ctx Alliance NFP
Providing education, support, advocacy, and promoting research for CTX patients, their families, and medical professionals who treat and study this rare disease Providing education, support, advocacy, and promoting research for CTX patients, their families, and medical professionals who treat and study this rare disease.
70
Lansdale
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Specifically Named Diseases Research
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35.
MECP2 DUPLICATION FOUNDATION
The MECP2 Duplication Foundation is a family founded organization providing support to the MECP2 Duplication community.
1339
TUCSON
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International Relief
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36.
FRIENDS OF IPWSO
Friends of IPWSO raises money to improve the lives of children and adults who are born with Prader-Willi Syndrome.
758
Eden Prairie