Identify rare syndromes and disorders affecting brain development, motor function, and cognitive health.

Detect inherited heart conditions early to optimize monitoring, prevent complications, and guide lifestyle and/or treatment decisions.

Pinpoint potential metabolic imbalances impacting growth, development, and overall well-being.

Uncover hereditary cancer risks to inform early screening and intervention strategies.

Address conditions passed down through generations, offering insights that help shape personalized care plans.

Includes Level 1A/1B pediatric clinical annotations describing variant-drug combinations with available prescribing guidance.