Similar organisations to DHPS FOUNDATION
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Professional Societies & Associations
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28.
Suneel Research Foundation
Our mission is to spread awareness about Duchenne Muscular Dystrophy (DMD), raise funds to support treatments and find a cure for DMD.
490
Buffalo
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Medical Disciplines
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29.
Pediatric Neurotransmitter Disease Association Inc
The PND association is a disease organization representing children and families who are affected by a pediatric neurotransmitter disease.
200
Farmingdale
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Public Health Programs
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30.
United Pompe Foundation
SUPPORT RESEARCH FOR POMPE DISEASE AND HELP PATIENTS DEALING WITH POMPE DISEASE United Pompe Foundation The United Pompe Foundation was formed to assist patients andor their families with medical costs and other expenses that these patents and families face and may not be able to cover or fully cover through their insurance.
Fresno
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Other Philanthropy, Voluntarism, and Grantmaking Foundations N.E.C.
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31.
INTERNATIONAL CHILDRENS ANOPHTHALMIA NETWORK INC
ICAN a voluntary not for profit organization, is a group of families and professionals dedicated to lending support to individuals who want to learn more about microphthalmia and anopthalmia and associated genetic counseling.
Philadelphia
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Fund Raising and/or Fund Distribution
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32.
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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Fund Raising and/or Fund Distribution
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33.
Eleanor Kaplan Foundation Inc
To raise funds and awareness to develop cures for Ultra Rare Neurodegenerative Diseases.
Delray Beach
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Specifically Named Diseases
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34.
SETBP1 Society
President of SETBP1 Society and Parent Advocate for SETBP1-HD SETPB1 Society's mission is to provide support to individuals with SETBP1 haploinsufficiency disorde Our Mission is to provide support to individuals with SETBP1 disorder and their families, to promote discussion and fund research, and to bring awareness and education to the public.
1141
Austin
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Alliance/Advocacy Organizations
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35.
Finding Nori Foundation
The Finding Nori Foundation Home About Meet the Team Finding Joy Blog Resources Publications DONATE Contact Upcoming Events More Raising research funding for PAX5 and ALG13 related neurological disordersEmpowering families with ultra rare undiagnosed diseases to find answers Our Mission Our mission is to advance scientific research through fundraising and advocacy for ultra rare undiagnosed genetic disorders.
Gilbert
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International Relief
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36.
FRIENDS OF IPWSO
Friends of IPWSO raises money to improve the lives of children and adults who are born with Prader-Willi Syndrome.
758
Eden Prairie