• Museums & Museum Activities

Prader Willi Association of New England Inc

PWS is a non-inherited genetic disorder which is associated with a random deletion of the 15th chromosome.

DUP 15Q ALLIANCE

Through our work to raise awareness and promote research into chromosome 15q duplications, we seek to find targeted treatments so that affected individuals can live full and productive lives.

Ring14 USA Outreach Inc

Ring14 Syndrome, Rare disease, Rare epilepsy, nonprofit, support, advocacy, research Ring14 USA is nonprofit 501(c)(3) that supports children and families affected by the rare syndromes of the 14th chromosome, such as Ring14 syndrome.

• Fund Raising and/or Fund Distribution

Seventeen 22 Foundation

Nonprofit focused on providing financial assistance for neurofibromatosis families.

• Specifically Named Diseases

3Q29 Foundation

3q29 Foundation Creating a path to treatment for chromosome 3q29 syndromes through funding research communitybuilding and increasing access to information and resources.

• Fund Raising and/or Fund Distribution

Ava Grace Foundation

For UPD14 Home Ava Gracex27s Story Donate Families Caregivers Medical Professionals Upcoming Events More The Ava Grace Foundation Supporting Families Advancing Research of UPD14Uniparental Disomy of the 14th Chromosome Families Caregivers Information about UPD14 common signs and symptoms getting diagnosed and treatments.

• Specifically Named Diseases Research

THE FOCUS FOUNDATION INC

OUR FOCUS:Helping children who have* X & Y Variations* Dyslexia * DyspraxiaEarly Identification + Tar Early Awareness Detection Treatment for X Y Chromosomal Variation Disorders X Y Chromosomal Disorders 47 XXY 47 XYY 47 XXX Learn more about them.

• Services to Promote the Independence of Specific Populations

1P36 DELETION SUPPORT & AWARENESS

1p36 Deletion Support & Awareness Support, Awareness & Education to improve the lives of individuals affected by 1p36 Deletion Syndrome Support Awareness and Education to improve the lives of individuals affected by 1p36 deletion syndrome If you have a loved one affected by 1p36 deletion syndrome were here to help 1p36 deletion syndrome occurs in approximately 1 in 5000 to 10000 live births and 1p36 Deletion Support Awareness is honored to currently serve hundreds of families affected by this rare genetic disorder.

• Birth Defects, Genetic Diseases Research

THE 11Q RESEARCH AND RESOURCE GROUP INC

home lifesaving protocols who we are frequently asked questions medical support donate More 11qRESEARCH RESOURCE GROUP WELCOMES YOU WHO WE ARE The mission of this website is to provide support and organizational efforts for the parents as well as friends and family of all children with 11th chromosome abnormalities including deletions monosomy duplications trisomy and translocations.

• Specifically Named Diseases Research

MECP2 DUPLICATION FOUNDATION

The MECP2 Duplication Foundation is a family founded organization providing support to the MECP2 Duplication community.