Similar organisations to Smashsmard, Inc.
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Hospitals and Primary Medical Care Facilities
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199.
 
Center for Medical Technology Policy
Center for Medical Technology Policy Home of #GPC (Green Park Collaborative), a multi-stakeholder forum developing #CoreOutcomeSets for clinical trial design.
423
Baltimore
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Single Organization Support
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200.
 
Greg Marzolf Jr Foundation
Fund research to find a cure for Neuromuscular disease Menu Last year the University of Minnesota MD Center was named the Greg Marzolf Jr.
St Paul
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Fund Raising and/or Fund Distribution
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201.
 
RARE GENOMICS INSTITUTE INC
RGI is a non-profit organization that provides research to families in need of diagnosis & treatment for rare genetic diseases.
13311
Los Angeles
MOWAT-WILSON SYNDROME FOUNDATION
This is the official page for the Mowat-Wilson Syndrome Foundation.
2800
Madison
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Birth Defects, Genetic Diseases
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203.
 
Project 8p Foundation
Project 8p aims to accelerate the translation of scientific research into therapies and treatment and advocate for the 8p community.
1500
New York
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Birth Defects, Genetic Diseases
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204.
 
The PolG Foundation
The mission of The POLG Foundation is to support and accelerate research to find effective treatments and a cure for PolG mitochondrial disorders.
New York
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Heart and Circulatory
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205.
 
Wittek Research Foundation for Hypertrophic Cardiomyopathy Inc
Dedicated to supporting research that will transform the prevention, diagnosis, and treatment of Hypertrophic Cardiomyopathy Dedicated to supporting research that will transform the prevention diagnosis and treatment of HCM Learn More Our Goals Our goal is to promote rapid identification and development of new innovative treatments for Hypertrophic Cardiomyopathy that will modify or eradicate the disease.
Tenafly
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Fund Raising and/or Fund Distribution
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206.
 
CURE RARE DISEASE INC
Nonprofit biotech leading a global collaboration to develop life-saving medicines for rare diseases Revolutionizing UltraRare Disease Treatment through Innovation and Collaboration Revolutionizing UltraRare Disease Treatment through Innovation and Collaboration What Wex27re Working Towards We envision a future where every patient has access to treatment.
8226
WOODBRIDGE
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Public Foundations
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207.
 
CURING RETINAL BLINDNESS
Welcome to our mission of bringing sight to children who are blind or visually impaired due to CRB1 retinal disease.
1379
SALEM






