• Birth Defects, Genetic Diseases Research

• 64.

Center for Human Genetics Inc

TO FUNCTION AS A LOCAL AND NATIONAL CLINIC AND DIAGNOSTIC REFERENCE RESOURCE FOR BIRTH DEFECT AND GENETIC DISORDERS; TO PROVIDE TECHNOLOGY AND SERVICES TO REFERRING PHYSICIANS AND PATIENTS FOR THE BENEFIT OF ALL PERSONS SUFFERING FROM ILLNESS, DEFECTS OR DISORDERS; TO TEACH MEDICAL STUDENTS, RESIDENTS, FELLOWS AND OTHER PERSONNEL ENGAGED IN HEALTH SERVICES AND HEALTH EDUCATION; TO ADVANCE SCIENTIFIC KNOWLEDGE THROUGH RESEARCH; TO TAKE ACTIVE PART IN THE PLANNING FOR AND THE PROMOTION OF THE SPECIFIC GENETIC AND GENERAL MENTAL AND PHYSICAL HEALTH AND HUMAN NEEDS AND INTERESTS OF THE LOCAL AND NATIONAL PATIENT POPUATION AND THEIR PHYSICIANS; TO PROVIDE SERVICES RELATED TO GENETICS; TO GATHER DATA AND ANALYZE IT FOR THE PURPOSE OF SHARING IT GENERALLY WITH THE LOCAL, NATIONAL AND INTERNATIONAL MEDICAL COMMUNITIES; TO IMPROVE AND DEVELOP TESTING PROTOCOLS AND KNOWLEDGE AND TO SHARE SUCH RESULTS FREELY AND OPENLY; TO ESTABLISH, OWN, OPERATE, CONDUCT OR MAINTAIN FACILITIES FOR TEACHING.

The Global Foundation for Peroxisomal Disorders

The GFPD's mission is to improve the lives of individuals with peroxisomal disorders by funding research, championing scientific collaboration, and empowering families and professionals through educational programs and support services.

• Eye Diseases, Blindness & Vision Impairment

• 66.

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.

• Fund Raising and/or Fund Distribution

• 67.

Seventeen 22 Foundation

Nonprofit focused on providing financial assistance for neurofibromatosis families.

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

• 68.

Hereditary Neurological Disease Centre Inc

Official Twitter for Genentech. See our community guidelines here: https://t.

• Alliance/Advocacy Organizations

• 69.

Rare Sisters Batten Foundation Inc

A rare, fatal, neurological disease that affects sisters Cecilia and Lilly.

• Birth Defects, Genetic Diseases Research

• 70.

International FOXP1 Foundation

Our mission is to build a global community that empowers and supports families and individuals with FOXP1 syndrome by sharing knowledge, inspiring hope, supporting research, and raising awareness.

• Alliance/Advocacy Organizations

• 71.

Baker-Gordon Syndrome Foundation

The BakerGordon Syndrome Foundation was founded to help families affected by this syndrome make connections with one another.

Lightning and Love Foundation

Founder of Lightning and Love foundation and mom to two ultra-rare THAP12 genetic epilepsy disease daughters searching for a cure.