• Birth Defects, Genetic Diseases

• 109.

Feingold Center for Children

The Genesis Foundation for Children funds clinical care and therapy for children born with complex genetic disorders and rare diseases.

• Specifically Named Diseases Research

• 110.

PROJECT ALIVE

A Hunter syndrome research and advocacy foundation.

• Birth Defects, Genetic Diseases

• 111.

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

• 112.

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.

• Human Service Organizations

• 113.

Yoey S Hope Inc

PUBLIC EDUCATION AND AWARENESS ON WOLF-HIRSCHHORN SYNDROME AND CHARITABLE SUPPORT FOR FAMILIES OF CHILDREN WITH WOLF-HIRSCHHORN SYNDROME.

• Fund Raising and/or Fund Distribution

• 114.

Patrick Allen Melvin Foundation

Partnering with nonprofit organizations and charities to raise funds and awareness for their cause.

Rare New England Inc

Rare New England's Mission is to bring together New England patients and families touched by rare and complex disorders.

• Fund Raising and/or Fund Distribution

• 116.

Chloe Strong Foundation

The Chloe Strong Foundation The Chloe Strong Foundation is a 501c3 nonprofit organization that exists to improve the quality of life for those that struggle with the rare neurological disorder Rett Syndrome by providing financial assistance support and prayers.

• Birth Defects, Genetic Diseases

• 117.

HNRNP FAMILY FOUNDATION

Nonprofit dedicated to serving those impacted by HNRNP-Related Rare Neurodevelopmental Disorders through supporting community and research Home Donate Events Learn Projects Join our Registry Join our Researcher Registry Shop Contact and Connect Submit your story HNRNPC Item HNRNPH1RNDD HNRNPH2RNDD More Our Mission The HNRNP Family Foundation is dedicated to improving the lives of patients and families around the world that live with rare HNRNPRelated Neurodevelopmental Disorders HNRNPRNDDs.