Jewish Genetic Disease Resources
Places to go for for testing, support, and help
551 Fifth Avenue, Suite 520
New York, NY 10017
Bachmann-Strauss Dystonia & Parkinson Foundation funds scientific research seeking to understand the causes of, and to find potential cures to, the movement disorders dystonia and Parkinson’s disease.
7095 Hollywood Boulevard #583
Los Angeles, CA 90028
The Bloom's Syndrome Foundation funds research aimed at the development of a therapy for Bloom’s syndrome and the prevention of its complications, primarily the significant risk of developing cancers at early ages.
450 West End Avenue, #6A
New York, NY 10024
The Canavan Foundation works to prevent Canavan disease through education and testing, and supports research to find a treatment for the disease.
88 Route 37
New Fairfield, CT 06812
The Canavan Research Foundation supports research aimed at curing Canavan disease and other genetic brain diseases.
Mount Sinai Medical Center
New York, NY 10029
The Center for Jewish Genetic Diseases works to improve the diagnosis and treatment of Jewish genetic diseases, as well as the counseling of patients and their families, and to conduct intensive research to combat these diseases.
Ben Gurion Way
30 South Wells Street
Chicago, IL 60606
The Center for Jewish Genetics works to provide public and professional education and to empower community members to seek out information and prevention strategies on Jewish genetic disorders and hereditary cancers. Subsidized screening programs are available; contact Tarynbrickman@Juf.org
917 Bethany Mountain Road
Cheshire, CT 06410
The Children's Fund for Glycogen Storage Disease Research raises money for research aimed at finding a cure for glycogen storage disease, type 1.
12730 Triskett Road
Cleveland, OH 44111
The Cure Tay-Sachs Foundation funds research seeking treatments and a cure for Tay-Sachs disease.
315 West 39th Street, Suite 701
New York, NY 10018
The Dysautonomia Foundation supports medical treatment, research, public awareness and social services for the benefit of people afflicted with familial dysautonomia.
1 East Wacker Drive, Suite 2810
Chicago, IL 60601
Fax: (312) 803-0138
The Dystonia Medical Research Foundation seeks to advance research for treatments for dystonia, promotes awareness and education, and provides support to affected individuals and their families.
1801 Willamette Street, Suite 200
Eugene, OR 97401
The Fanconi Anemia Research Fund works to find effective treatments for Fanconi anemia and to provide education and support services to affected families.
121 S. Estes Drive, Suite 205D
Chapel Hill, NC 27514
FD Hope funds research into potential treatments and cures for familial dysautonomia, provides support to FD families and patients, and promotes education and awareness of the disease.
1425 Madison Avenue, Box 1498
New York, NY 10029
The Genetic Disease Foundation supports research, education and the prevention of genetic diseases.
P.O. Box 52
Rye, NY 10580
Jacob’s Cure supports research into treatments for Canavan disease.
450 West End Avenue
New York, NY 10024
The Jewish Genetic Disease Consortium brings together organizations that combat Jewish genetic diseases in order to strengthen education and awareness, as well as to encourage and facilitate genetic testing for carrier status.
719 East 17th Street
Brooklyn, NY 11230
The ML4 Foundation supports medical research dedicated to developing effective treatments and a cure for Mucolipidosis type IV.
2227 Idlewood Road, Suite 12
Tucker, GA 30084
The National Gaucher Foundation funds research on Gaucher disease, promotes education and awareness, supports legislative issues and provides outreach programs.
P.O. Box 49
401 Madison Avenue, Suite B
Fort Atkinson, WI 53538
The National Niemann-Pick Disease Foundation supports research to find a cure or treatments for all types of Niemann-Pick disease and provides support services to individuals and families affected by the disease.
2001 Beacon Street, Suite 204
Brighton, MA 02135
The National Tay-Sachs and Allied Diseases Association promotes the prevention and treatment of Tay-Sachs in all its forms as well as other related genetic disorders, and provides support services to affected families and individuals.
500 West 185th Street, Belfer Hall 707
New York, NY 10033
The Program for Jewish Genetic Health is a centralized resource for the Jewish community and its future generations, addressing Jewish genetic health concerns from before birth through old age. Servicing the community and listening to its needs…evolving and adapting as community needs grow and change.
24701 La Plaza, #201
Dana Point, CA 92629
The RARE Project mobilizes rare disease patients, parents and patient-advocates in order to bring about more effective and efficient development of rare disease therapies.
2304 Highland Drive
Sycamore, IL 60178
The United Leukodystrophy Foundation supports individuals suffering from various types of leukodystrophies, such as Canavan disease, and provides assistance for their families. It also helps with research into these diseases.
Albert Einstein Medical Center
Philadelphia, PA 19141
The Victor Center for Jewish Genetic Diseases provides education, genetic counseling and carrier screening for Jewish genetic diseases. Victor Centers are located in Philadelphia, Boston and Miami.