• 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.

• Medical Disciplines

• 65.

Pediatric Neurotransmitter Disease Association Inc

The PND association is a disease organization representing children and families who are affected by a pediatric neurotransmitter disease.

• Birth Defects, Genetic Diseases

• 66.

Regenerative Medicine Foundation Inc

Official account of Regenerative Medicine Foundation, hosts of The World Stem Cell Summit - the world's flagship stem cell & biotech event.

• Professional Societies & Associations

• 67.

Healthspan Action Coalition Inc

The mission is to advance biomedical research related to aging, longevity and healthspan.

Dlg4 Research Fund

DLG4-related Synaptopathy / SHINE Syndrome *Managed by the board of the DLG4 SHINE Foundation A page for people interested in learning more about DLG4-related Synaptopathy / SHINE Syndrome *Managed by the board of the DLG4 SHINE Foundation Mission To find specific treatment options and a cure for DLG4 patients by building a collaborative network of patients, families, clinicians and scientists that will work together to raise awareness and accelerate the understanding, diagnosis and treatment of DLG4 related synaptopathy.

Texas Neurofibromatosis Foundation

We’re a community of NF patients, parents, doctors and advocates who want to listen, support or help you as we can.

CureSHANK

CureSHANK's mission is to accelerate the development of treatments and cures for Phelan-McDermid Syndrome and other SHANK-related disorders.

• Medical Specialty Research

• 71.

FIBROMUSCULAR DYSPLASIA SOCIETY OF

The recognized leader in the support of Fibromuscular Dysplasia (FMD) awareness, education and research.

• Birth Defects, Genetic Diseases

• 72.

NF2 Biosolutions

NF2 patient led nonprofit dedicated to funding research, and supporting those affected by NF2-related schwannomatosis NF2 BioSolutions, is a 100% volunteer-run, nonprofit organization that funds research for NF2 Accelerating Novel Therapy Research for Neurofibromatosis Type 2 Gene Therapy is changing the world of genetic diseases.