What this tool is
A structured family health history that detects patterns— e.g. an early-onset coronary pattern, a Lynch-spectrum cancer pattern, a type-2 diabetes cluster — and turns them into discussion prompts for a clinician, plus concrete questions to ask the rest of your family to fill the gaps. Modelled after the CDC’s My Family Health Portrait tradition.
What this tool is not
Not a genetic test, not a genetic risk score, not a diagnosis. Family history is one input among many; only a clinician (and where relevant, a genetic counselor) can interpret it in context. Outputs are framed as patterns to discuss, never as findings of disease. This tool will never recommend supplements based on family history.
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Why patterns, not predictions
Cause-of-death records are often inaccurate, recall is patchy, and shared environment (diet, smoking, geography) blurs the “genetic” signal. Pattern-level framing is honest about what family history can and can’t tell you, and matches how clinicians actually use it.
Adopted / estranged / donor-conceived
Many people only know part of their family history. TheWhat’s missing section is built for that: it tells you which gaps would change the picture and which relatives to ask next, instead of treating partial answers as a failure.
Privacy
Family health data is sensitive. Your answers are stored only in this browser, scoped to the active profile. Nothing is uploaded. See transparency for the network-level audit.
For your clinician
Use the printable family history sheet to bring a one-page summary to your next visit — the same content as the on-screen report, formatted for A4.
How this tool was built
Rule-based and deterministic; patterns are derived from public guidance (USPSTF, ACC/AHA, ADA, ACG, AAD, Alzheimer’s Association). The rules engine is open source. This tool has not been clinically reviewed; see methodology for how Almavivo’s tools are built and where they stop.