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Distributes information on prevention of birth defects. Provides information on birth defects and genetic disorders such as Achondroplasia, Autism Spectrum Disorder, Cerebral Palsy, Cleft Lip and Cleft Palate, Clubfoot, chromosomal conditions, Congenital Adrenal Hyperplasia, Congenital Heart Defects and CCHD, Down Syndrome, Fragile X, genital and urinary tract defects, hearing loss, neural tube defects, Neurofibromatosis, PKU, Polio, Post-Polio Syndrome, Rh Disease, Sickle Cell, Spina Bifida, Tay-Sachs, Thalassemia, and rare birth defects.

Distributes information on prevention of birth defects. Provides information on birth defects and genetic disorders such as Achondroplasia, Autism Spectrum Disorder, Cerebral Palsy, Cleft Lip and Cleft Palate, Clubfoot, chromosomal conditions, Congenital Adrenal Hyperplasia, Congenital Heart Defects and CCHD, Down Syndrome, Fragile X, genital and urinary tract defects, hearing loss, neural tube defects, Neurofibromatosis, PKU, Polio, Post-Polio Syndrome, Rh Disease, Sickle Cell, Spina Bifida, Tay-Sachs, Thalassemia, and rare birth defects.

Education and outreach to Amish families includes information about of the importance of testing newborn children, consistent medical treatment of children, dietary requirements, etc. Research is done on metabolic and genetic disorders, and the findings are shared with medical professionals and other researchers. Special attention is paid to diseases prevalent in the Amish community. Speakers are available for any civic, church, community, or professional groups, and a newsletter is published twice a year.

Education and outreach to Amish families includes information about of the importance of testing newborn children, consistent medical treatment of children, dietary requirements, etc. Research is done on metabolic and genetic disorders, and the findings are shared with medical professionals and other researchers. Special attention is paid to diseases prevalent in the Amish community. Speakers are available for any civic, church, community, or professional groups, and a newsletter is published twice a year.

Provides information on rare, orphan, neglected, and genetic diseases. Links to journal publications, conferences, support groups, treatments, and clinical trials are provided on web site. Answers questions about specific diseases, rare diseases in general, and undiagnosed conditions.

Provides information on rare, orphan, neglected, and genetic diseases. Links to journal publications, conferences, support groups, treatments, and clinical trials are provided on web site. Answers questions about specific diseases, rare diseases in general, and undiagnosed conditions.