Similar organisations to International FOXP1 Foundation
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Museums & Museum Activities
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190.
Prader Willi Association of New England Inc
PWS is a non-inherited genetic disorder which is associated with a random deletion of the 15th chromosome.
1171
North Reading
BEYOND BATTEN DISEASE FOUNDATION
Mission: eradicate Batten disease. Batten disease is a fatal neurodegenerative disorder that takes away childhood, and then takes away.
4770
Austin
GILLETTE CHILDRENS SPECIALTY HEALTH CARE
We are a global beacon of care for patients with brain, bone and movement conditions.
85000
Saint Paul
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Fund Raising and/or Fund Distribution
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193.
Sdhb Coalition Inc
Our mission is to educate healthcare professionals and patients on the SDHB genetic germline mutation as well as its role and impact in this orphan disease SEE SCHEDULE O ABOVE Vision Mission Our mission is to educate healthcare professionals and patients on the SDHB genetic germline mutation as well as its role and impact in this orphan disease namely Pheochromocytoma and Paraganglioma.
501
Doylestown
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Research Institutes and/or Public Policy Analysis
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194.
Riaan Research Initiative Inc
501(c)(3) non-profit organization hunting for a cure for rare and life-limiting genetic diseases that hurt children, starting with Cockayne syndrome.
684
Oakland Gardens
Beck Fahrner Syndrome Foundation
Our mission is to accelerate full spectrum research to cure Beck-Fahrner Syndrome (TET3 deficiency) and to empower affected families with information, knowledge, and connectivity.
Anoka
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Nonmonetary Support N.E.C.*
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196.
N 1 Collaborative Inc
OUR MISSION IS TO MAKE INDIVIDUALIZED MEDICINES ROUTINELY AND RAPIDLY ACCESSIBLE TO RARE DISEASE PATIENTS WORLDWIDE.
Somerville
ANGELMAN SYNDROME FOUNDATION INC
Angelman Syndrome Foundation advances the awareness and treatment of Angelman Syndrome through education, information, research and support.
31057
Aurora
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Nonmonetary Support N.E.C.*
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198.
SPOONBILL FOUNDATION
Finding a solution for PKAN Spoonbill Foundation and our sister organization Stichting Lepelaarwere founded with the goal to discover develop and deliver therapeutics for PKAN and all NBIA disorders in partnership with the NBIA community as swiftly as possible and at the lowest cost.
Portland





