Your Family’s Health, Seamlessly Connected
Heredimap is critical for identifying inherited conditions which is rarely integrated into clinical records. Gathering and organizing information across multiple relatives and sources is time-consuming and complex, making cascade testing inefficient and often delayed.
Our solution streamlines the collection and integration of family health data by automating data aggregation from multiple relatives and sources, optimizing cascade testing workflows, and providing clinicians with a clear, organized view—reducing logistical burdens and accelerating genetic risk assessment.
Heredimap also complies with the Standardized human pedigree nomenclature to provide users with a clear and accurate visualization of genetic inheritance. This nomenclature is essential for the identification and study of genetic relationships between individuals, enabling researchers and healthcare professionals to better understand the genetic implications of inherited diseases.
