Virtual assistant designed to support clinical genetics and genetic counselors, neonatology, pediatrics, maternal–fetal medicine, rare disease units, pediatric cardiology, pediatric neurology, pediatric surgery, radiology, genetics laboratories, primary care, and emergency medicine in the initial assessment of patients with multiple congenital anomalies and/or dysmorphic features, syndromic phenotyping, test prioritization, genetic interpretation, initial management, and referral, based on current evidence and clinical practice guidelines as of February 2026.