• Birth Defects, Genetic Diseases Research

• 532.

International Association for Chronic Fatigue Syndrome-Me

THE MISSION OF IACFS/ME IS TO PROMOTE, STIMULATE AND COORDINATE THE EXCHANGE OF IDEAS RELATED TO CHRONIC FATIGUE SYNDRONE(CFS) AND FIBROMYALGIA(FM) RESEARCH, PATIENT CARE AND TREATMENT IN ADDITION, THE IACFS/ME PERIODICALLY REVIEWS THE CURRENT RESEARCH AND TREATMENT LITERATURE AND MEDIA REPORTS FOR THE BENEFIT OF SCIENTISTS, CLINICIANS AND PATIENTS.

VASCULAR CURES

Transforming vascular health outcomes for all through patient empowerment, collaboration, and research Transforming vascular health outcomes for all through patient empowerment, collaboration and research Vascular Cures envisions a world where all people can enjoy vascular health.

• Birth Defects, Genetic Diseases

• 534.

National Society of Genetic Counselors Inc

About MNGCA About Genetic Counseling Membership Education Conference Contact More Welcome tothe Minnesota Genetic Counselors Association A Chapter of the National Society of Genetic Counselors About MNGCA Welcome to the Minnesota Genetic Counselors Association.

• Heart and Circulatory

• 535.

International Andreas Gruentzig Society

The International Andreas Gruentzig Society is an international educational society of physicians and scientists interested in cardiovascular health sciences and related fields.

• Birth Defects, Genetic Diseases

• 536.

CTNNB1 SYNDROME AWARENESS WORLDWIDE

CTNNB1 Syndrome refers to complications resulting from either a mutation or deletion of the CTNNB1 gene.

• Professional Societies & Associations

• 537.

Hemophilia Foundation of Northern California

Hemophilia Foundation of Northern California - nonprofit organization serving needs of people with hemophilia, VWD, and all other bleeding disorders Creating a lifeline of community and support for families affected by bleeding disorders.

• Group Home (Long-Term, Primarily Assisted Living)

• 538.

Prader-Willi Homes of California

PraderWilli Syndrome Center France ABOUT PWS PraderWilli Syndrome PWS is a complex rare and random genetic disorder that affects one in twelve to fifteen thousand people.

• Counseling Support Groups

• 539.

NATIONAL COALITION FOR WOMEN WITH HEART

WomenHeart empowers women to take charge of their heart health.

• Fund Raising and/or Fund Distribution

• 540.

THE CHAMP FOUNDATION

Mission The Champ Foundation supports research toward better treatment and a cure for single largescale mitochondrial deletion syndromes SLSMDS like Pearson syndrome.