This funding opportunity supports research to expand understanding of the natural history of disorders included or potentially included in newborn screening programs. Funded activities include characterizing symptom development, establishing genotype-phenotype correlations, identifying modifying factors, improving diagnostic accuracy, facilitating clinical trials, and developing longitudinal data collection systems or patient registries.
Eligible applicants include a wide range of organizations such as for-profit entities (excluding small businesses), state and local governments, tribal organizations, educational institutions, nonprofits, and small businesses. Specific eligibility details should be confirmed with the funding source.
