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.

Cancer Genomics Consortium

The CGC represents clinical cytogeneticists, molecular geneticists, and molecular pathologists to promote best practices & education in clinical cancer genomics The CGC is focused on education and promoting best practices in clinical cancer genomics.

• Human Services - Multipurpose & Other N.E.C.

• 39.

Charlotte Mothers of Multiples Incorporated

Charlotte Mothers of Multiples (CMOMS) is a 501(c)3 providing support for families raising multiples.

• Birth Defects, Genetic Diseases

• 40.

International Rett Syndrome Association, Inc.

We are transforming lives every day in our fight to treat and cure Rett syndrome and better the lives of families living with this devastating disorder.

• Eye Diseases, Blindness & Vision Impairment

• 41.

BCM FAMILIES FOUNDATION

To eradicate Blue Cone Monochromacy (BCM), to provide financial support for research, projects, activities and organizations related to the diagnosis, treatment and/or cure of Blue Cone Monochromacy ("BCM"),to establish networks and synergies with other groups and organizations dedicated to eye and/or other rare disease issues, to make support and resources available to BCM patients and their involved families, and to educate the general public regarding BCM.

AXYS

Association for X and Y Chromosome Variations.

• Specifically Named Diseases Research

• 43.

MECP2 DUPLICATION FOUNDATION

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

• Fund Raising and/or Fund Distribution

• 44.

BFLS Incorporated

Mom on a mission to raise awareness and funds for research for the rare genetic disorder Börjeson-Forssman-Lehman Syndrome or BFLS� Born Fierce.

• Birth Defects, Genetic Diseases

• 45.

GRIN2B FOUNDATION

Our goal is to offer support and share research to the small, but growing community of children diagnosed with alterations on their GRIN2B gene.