• Birth Defects, Genetic Diseases Research

• 73.

Jewish Genetic Diseases Center of Greater Phoenix

BRCA Positive I BRCA Support and Education I BRCA BRCA Positive I BRCA Support and Education I BRCA Our Mission To Provide Education Screening and Support to empower the Jewish Community to make informed decisions regarding genetic disorders WE OFFER THREE PROGRAMS TO SERVE THE COMMUNITY PRECONCEPTION COUNSELING AND SCREENING WE PROVIDE FREE GENETIC COUNSELING AND HIGHLY SUBSIDIZED TESTING FOR COUPLES WHO ARE HAVING MORE CHILDRENSEE THE GET SCREEDED.

• Specifically Named Diseases

• 74.

Cardio Facio Cutaneous International

CFC International is dedicated to the support, research and treatment of individuals living with CFC Syndrome.

Hemophilia Association of NY

The Hemophilia Association of New York has provided people with bleeding disorders support and aid since 1952.

• Alliance/Advocacy Organizations

• 76.

Team Telomere

An international community for telomere biology disorders.

• Birth Defects, Genetic Diseases

• 77.

Sickle Cell Association of Houston, Inc,

Providing services and supportive resources to those suffering from this overwhelming disease.

• Specifically Named Diseases

• 78.

Niemann-Pick Childrens Fund

Niemann-Pick Children's Fund, Inc. was organized in December of 2008 in order to raise awareness of Niemann-Pick Disease Type C and its affect on families in America; to raise money to promote research to find treatments or a cure for Niemann-Pick Disease Type C: and to provide support to individuals and families affected by this disease through existing channels.

Myhre Syndrome Foundation

Myhre Syndrome Foundation is dedicated to serving Myhre syndrome families by providing a network of hope and support.

• Birth Defects, Genetic Diseases

• 80.

The PolG Foundation

The mission of The POLG Foundation is to support and accelerate research to find effective treatments and a cure for PolG mitochondrial disorders.

• Health - General & Rehabilitative N.E.C.

• 81.

4P-Support Group

Our mission is to serve our membership by providing information, education and support; uniting families, researchers, and professionals; and promoting awareness and understanding of 4p- syndrome, with Wolf-Hirschhorn Syndrome as the main condition, and the related 4th chromosome abnormalities.