Similar organisations to MOONSHOTS FOR UNICORNS
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Birth Defects, Genetic Diseases Research
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190.
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.
3700
Georgetown
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Fund Raising and/or Fund Distribution
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191.
Chase The Cure Inc.
Chase the Cure Inc was created to serve the Niemann Pick Type C Community.
Cumberland
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Birth Defects, Genetic Diseases Research
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192.
Fam177a1 Research Fund
Founder and President, FAM177A1 Research Fund The mission of the FAM177A1 Research Fund is to improve the lives of those affected by FAM177A1 Associated Disorder through research and development of transformative therapies.
434
Mercer Island
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Fund Raising and/or Fund Distribution
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193.
The TBCD Foundation
The TBCD Foundation is a non-profit organization for and by the TBCD Disorder community to raise funds and awareness in order to pursue effective treatments and a cure for TBCD.
280
Gotha
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Fund Raising and/or Fund Distribution
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194.
FOUNDATION FOR FELINE RENAL RESEARCH LTD
Love cats. Join our quest for a cure. Kidney Disease kills 1 in 3 cats--we raise awareness, & provide grants for the best evidence-based humane research.
2637
Hicksville
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Birth Defects, Genetic Diseases Research
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195.
Alstrom Angels Corp
www. alstromangels. org Dedicated to raising funds for Alstrom Syndrome genetic and medical research, increasing awareness of the rare disease among the general public and medical communities, and improving family support for those affected by the Syndrome.
2206
Lubbock
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Birth Defects, Genetic Diseases
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196.
LOVE AN ANGEL FOUNDATION
The Love an Angel Foundation (LAAF) is a 501(c)3 nonprofit organization working to meet the needs of Do you know any Angels.
205
NEW FRANKLIN
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Brain Disorders
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197.
THE PIERCE FAMILY FRAGILE X FOUNDATION
The Pierce Family Fragile X Foundation is a non-profit created to fund research, development of treatments, and community awareness to find a cure for Fragile X Created to fund dedicated research, development of treatments, and community awareness for Fragile X The Pierce Family Fragile X Foundation is a nonprofit organization that has been created to fund dedicated research development of treatments and community awareness in support of finding a cure for Fragile X Syndrome affecting our beautiful boys Graham and Reid.
1717
WINCHESTER
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Fund Raising and/or Fund Distribution
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198.
THE CHAMP FOUNDATION
Mission The Champ Foundation supports research toward better treatment and a cure for single largescale mitochondrial deletion syndromes SLSMDS like Pearson syndrome.
DURHAM