Rare Genomics Institute

Tags: Amyotrophic Lateral Sclerosis (ALS), Angel Man Syndrome, Asperger's Disorder(s), Autonomic Nerve Disorder(s), Birth Defects & Genetic Diseases, Brain Disorder(s), Child Advocacy Centers, Child Health Care, Childhood Diseases (all), Childhood Disorders (all), Down Syndrome, Genetics, Hemophilia, Nervous System Disorder(s), Neuronal Migration Disorder(s), Parkinson's Disease, Prader-Willi Syndrome, Sickle-cell Disease, Triplet Repeat Genetic Disorder(s), Turner Syndrome, X Chromosome Disorder(s), Y Chromosome Disorder(s)

Rare Genomics Institute (RGI) is a non-profit organization that provides cutting-edge research to families in need of diagnosis and treatment for rare genetic diseases. Very little is invested into the necessary customized research and diagnosis for these diseases, leaving an estimated 20 million Americans in need today.