Similar organisations to The Telomere Project
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Birth Defects, Genetic Diseases
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91.
Boomer Esiason Foundation
Fighting Cystic Fibrosis - Advocacy - Education - Fundraising We are a group of passionate, dedicated individuals who work every day to raise money, awareness, and support for the cystic fibrosis community.
38047
Garden City Park
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Fund Raising and/or Fund Distribution
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92.
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
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Lung
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93.
Alpha 1 Association
Our mission is to increase awareness of and find a cure for Alpha-1 Antitrypsin Deficiency.
24001
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Fund Raising and/or Fund Distribution
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94.
Curemito
Our mission is to unite the global Leigh syndrome community to accelerate patient-centered research, treatments, and cures.
3559
Pasadena
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Fund Raising and/or Fund Distribution
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95.
Rare Village Foundation
TO FIGHT FOR CURES FOR RARE DISEASES AND EMPOWER INDIVIDUALS WITH RARE DISEASES TO LIVE THEIR BEST LIVES THROUGH LOCAL COMMUNITY EDUCATION, INSPIRING ADVOCACY, AND TIMELY CONNECTION TO CRITICAL RESEARCH THAT LEADS TO CURES We Empower Families to Create Cures for Rare Disease.
Mckinney
Alagille Syndrome Alliance
The Alagille Syndrome Alliance is an international support and advocacy network for people with ALGS and their families.
387
Collierville
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Birth Defects, Genetic Diseases
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97.
Iqsec2 Research and Advocacyfoundation
Welcome to IQSEC2. ORG Research and Advocacy Foundation MISSION STATEMENT Vision In the next 10 years we will dramatically improve the quality of life for those affected by IQSEC2 mutations through 1 the establishment and dissemination of standard treatment and therapy protocols to medical practitioners and therapists worldwide 2 support of research and development of new and innovative treatments for IQSEC2 related diseases and 3 uplift support all loved ones of those affected by IQSEC2 through an advocate community and its allies.
Frisco
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Specifically Named Diseases
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98.
Project CASK
An innovative rare disease non-profit driving breakthroughs in treatments and a cure for CASK gene disorders.
502
New York City
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Birth Defects, Genetic Diseases
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99.
HNRNP FAMILY FOUNDATION
Nonprofit dedicated to serving those impacted by HNRNP-Related Rare Neurodevelopmental Disorders through supporting community and research Home Donate Events Learn Projects Join our Registry Join our Researcher Registry Shop Contact and Connect Submit your story HNRNPC Item HNRNPH1RNDD HNRNPH2RNDD More Our Mission The HNRNP Family Foundation is dedicated to improving the lives of patients and families around the world that live with rare HNRNPRelated Neurodevelopmental Disorders HNRNPRNDDs.
162
SEATTLE






