Similar organisations to JACKSON LABORATORY
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Alliance/Advocacy Organizations
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181.
Hht Foundation International Inc
Cure HHT is the only organization in the US advocating for research, education and a cure for Hereditary Hemorrhagic Telangiectasia, Osler-Weber-Rendu Syndrome The official Facebook page for Cure HHT, the world's leading organization working to raise awareness The mission of the HHT Foundation International is to find a cure for HHT while saving the lives and improving the well-being of individuals and families affected by HHT.
11458
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Fund Raising and/or Fund Distribution
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182.
Taylors Tale
Taylor's Tale is a public charity dedicated to the fight against CLN1 disease and other rare diseases.
3106
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Specifically Named Diseases
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183.
Joel A Gingras Jr Memorial Foundation Inc
PROVIDE FUNDING FOR RESEARCH IN THE PREVENTION AND CURE OF BRAIN TUMORS Supporting Brain Tumor Research since 1989 The mission of the JAG Fund is to celebrate the life of Joel A.
Chalfont
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Health - General & Rehabilitative N.E.C.
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184.
Genetic Disease Foundation Inc
The Genetic Disease Foundation (GDF) is a non-profit 501c(3) organization established in 1997 by patients and families affected by genetic disorders.
Parsippany
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Professional Societies & Associations
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185.
Molecular Psychiatry Association Inc
TO PROMOTE MOLECULAR PSYCHIATRY RESEARCH SAVE THE DATE 10TH BIENNIAL MOLECULAR PSYCHIATRY MEETING Registration and Submissions will open in May 2025.
Brentwood
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Specifically Named Diseases
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186.
Wylder Nation Foundation
WARRIORS in the Fight Against Lysosomal Storage Disorders.
1140
Scottsdale
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Birth Defects, Genetic Diseases Research
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187.
Rory Belle Foundation
We are a family run foundation established to raise funding and awareness for a gene therapy cure for the NARS1 disease.
264
Denver
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Fund Raising and/or Fund Distribution
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188.
Undiagnosed Diseases Network Foundation (UDNF)
Improving access to diagnosis, research, and care for all with undiagnosed and ultra-rare conditions.
3469
Washington
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Cultural/Ethnic Awareness
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189.
May5Foundation
The May5Foundation and founder Dr. Alexia Mays are committed to supporting the communities of sickle cell, grief & loss, thru research ,advocacy &awareness The May5Foundation is centered in the values of dedication to education,community and service WE DO AMAYSING THINGS Programs and Events Support Our Efforts Who We Are More Community Events 2024 Warrior of The Year .
493
New Orleans