BLUE NEVUS MELANOMA FOUNDATION

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Global Patient Registry

Uniting data to cure blue nevus

By contributing your clinical history, you provide the critical data needed to attract pharmaceutical interest, design clinical trials, and accelerate molecular oncology discoveries.

A close-up of a researcher in a clean-room laboratory environment looking at a monitor displaying genetic data sequences, soft natural window light, 35mm
A close-up of a researcher in a clean-room laboratory environment looking at a monitor displaying genetic data sequences, soft natural window light, 35mm
Rigorous Security

A secure global database

We maintain the highest standards of data protection. Your clinical information is fully de-identified before researchers analyze it, ensuring your privacy is absolute while mapping rare disease progression.

This centralized repository allows oncologists and pharmaceutical partners worldwide to study GNAQ and GNA11 mutations, identifying drug repurposing opportunities that would otherwise remain hidden.

Simple Enrollment

Three steps to contribute

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Consent Online

Share History

Accelerate Research

Review and sign our secure digital consent form to authorize the collection of your clinical history and tumor genetics safely.

Upload medical records or complete a brief questionnaire detailing your diagnosis, treatment history, and GNAQ/GNA11 mutation status securely.

Your de-identified data immediately joins the global registry, becoming securely accessible to verified oncology researchers worldwide.

Begin Enrollment

Become the missing link

Enrollment takes fifteen minutes. Your secure contribution directly drives the development of targeted therapies, drug repurposing, and molecular oncology discoveries.