Similar organisations to DUP 15Q ALLIANCE
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Alliance/Advocacy Organizations
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28.
NEW JERSEY CENTER FOR TOURETTE SYNDROME AND ASSOCIATED DISORDERS
As many as 1 in 50 individuals show signs of Tourette Syndrome – most of them undiagnosed, misdiagnosed or misunderstood.
4618
Somerville
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Birth Defects, Genetic Diseases
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29.
Tennessee Prader-Willi Association, Inc.
We provide support and information for people with PWS & their families.
640
Nashville
Cystinosis Research Foundation
The Cystinosis Research Foundation’s (CRF) mission is to find better treatments and a cure for cystinosis, a rare genetic disease that destroys every organ.
5116
Irvine
THE CLINIC FOR SPECIAL CHILDREN INC
A nonprofit comprehensive medical practice focused on treating & researching rare genetic disorders.
3100
Intercourse
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Fund Raising and/or Fund Distribution
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32.
Dravet Syndrome Foundation, Inc.
The mission of DSF is to raise funds for research into Dravet syndrome and related epilepsies, while offering support to patients and families.
18554
Cherry Hill
DDC CLINIC FOR SPECIAL NEEDS CHILDREN
DDC Clinic is a non-profit primary care, education, and research facility.
682
Middlefield
PRADER-WILLI CALIFORNIA FOUNDATION
Our vision is a A Full Life Without Limits for everyone with Prader-Willi syndrome.
3400
San Diego
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Specifically Named Diseases Research
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35.
THE FOCUS FOUNDATION INC
OUR FOCUS:Helping children who have* X & Y Variations* Dyslexia * DyspraxiaEarly Identification + Tar Early Awareness Detection Treatment for X Y Chromosomal Variation Disorders X Y Chromosomal Disorders 47 XXY 47 XYY 47 XXX Learn more about them.
1754
DAVIDSONVILLE
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Birth Defects, Genetic Diseases
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36.
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