Similar organisations to Rare Genes Movement
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Diseases, Disorders, Medical Disciplines N.E.C.
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1.
U R Our Hope
Non-profit serving individuals with undiagnosed & rare disorders through education, advocacy, and support in order to bring hope through knowledge, empowerment Assisting those with undiagnosed or rare disorders at any age and any stage.
2304
AUSTIN
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Birth Defects, Genetic Diseases
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2.
Gene Spotlight Inc
We are a nonprofit medical research and advocacy organization committed to spark breakthroughs in treatments and cures for rare genetic disorders, including lysosomal storage diseases, uncommon cancers and other orphan diseases.
MIAMI
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Fund Raising and/or Fund Distribution
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3.
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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Specifically Named Diseases Research
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4.
The Snow Foundation
A voice for rare disease, working towards a cure for Wolfram syndrome and developing novel therapies for diabetes, vision loss, hearing loss neurodegeneration.
3152
Clayton
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Fund Raising and/or Fund Distribution
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5.
Ellie White Foundation for Rare Genetic Disorders Inc
We will not give up until a cure for Wolfram syndrome is found for Ellie and the children suffering from this disorder.
1161
Centennial
Rare and Undiagnosed Network Inc
RUN for those affected with rare/undiagnosed conditions: Raise awareness.
4500
Salt Lake City
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Fund Raising and/or Fund Distribution
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7.
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
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Fund Raising and/or Fund Distribution
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8.
Childrens Rare Disease Organization Inc
Many children are living with a rare disease.
Potomac
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Fund Raising and/or Fund Distribution
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9.
The Children's Rare Disorders Fund
Dedicated to curing rare genetic disorders Founded in July 2022 by parents of a toddler affected by FOXG1, The CRD Fund focuses on under served communities in the rare disorder space.
32
New York






