Clinical Genomics
OrigenDx™
Comprehensive Newborn Screening
An advanced diagnostic tool that can detect inborn metabolic errors in newborns
Comprehensive Newborn Screening for a Healthier Future
OrigenDx™ empowers parents with peace of mind by detecting over 355 inherited metabolic and genetic conditions with more than 99% accuracy. Using next-generation sequencing, it enables early discovery, timely intervention, and better long-term outcomes for your child’s health.
Early Detection, Lifelong Benefits
Many babies with genetic disorders appear healthy at birth, but symptoms may only emerge later when treatment options are limited. OrigenDx™ ensures early diagnosis so parents can act before complications arise, enabling timely medical interventions and improving lifelong outcomes.
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Detects 355 inherited conditions not included in standard newborn screening programs
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Prevents irreversible complications through timely treatment
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Reduces emotional and financial burden on families
Trusted Accuracy, Complete Support
OrigenDx™ delivers results with exceptional accuracy through advanced sequencing and bioinformatics. Families are supported with clear reports, professional guidance, and actionable insights, ensuring they understand every step and can make informed decisions for their child’s future health.
