ONE TECHNOLOGY. THREE BREAKTHROUGHS.

Longitudinal Intelligence
for Healthcare, Families & Research

The world's first platform using TTT Framework to detect rare diseases earlier, track family health patterns, and generate privacy-safe research datasets

20+

Diseases Validated

Up to 17 Years

Earlier Detection

100%

Privacy Protected

Three Solutions. One Mission.

Catch rare diseases earlier. Protect patient privacy. Save lives.

Clinical Co-Pilot

For Physicians & Clinics

AI-powered rare disease detection that remembers every patient visit and catches patterns others miss

Auto-generates clinical documentation in seconds
Detects rare diseases 2-17 years earlier
Tracks symptoms & labs across multiple visits
Validated on 20+ diseases with peer-reviewed sources

Family Space

For Patients & Families

Private health tracking portal for families dealing with rare diseases or chronic conditions

Track symptoms for entire family in one place
Visual timelines showing health patterns over time
100% private - you control all your data
Spot genetic patterns across family members

Synthetic Cohorts

For Researchers & Pharma

Generate privacy-safe synthetic patient datasets for rare disease research and AI training

Generate 100s of patients in minutes, not years
Zero privacy risk - mathematically guaranteed
Clinically realistic (92% AI diagnostic accuracy)
FHIR R4 compatible for instant integration
POWERED BY TTT FRAMEWORK

One Technology Powers All Three

The TTT Framework is our proprietary longitudinal pattern recognition engine

Tempo

How fast is the disease progressing? Days, weeks, or years? Understanding disease speed narrows diagnosis possibilities.

Topology

Which organ systems are affected and in what order? Rare diseases have characteristic multi-system patterns.

Trajectory

Is it progressive, episodic, or stable? The disease trajectory creates a unique signature for each condition.