Lifetime reanalysis until diagnosis
Nearly 300 rare genetic diseases are discovered on average each year. Continuous reanalysis increases the chances of diagnosis for undiagnosed patients.
More than 20% of undiagnosed patients can receive diagnoses by reanalyzing the initial genetic test data with newly discovered gene-disease findings (Fung JLF et al., 2020).
3billion provides clinical genetic testing on nearly 20,000 genes and more than 7,000 rare genetic diseases for affected patients.
The test includes unlimited reanalysis that takes into account newly discovered rare diseases until diagnosis.
Try our symptom search
- Enter all symptoms you are experiencing in the search box.
- As you type, you will be given options of HPO terms closest to the entered symptom. HPO terms must be selected for the search.
- Enter as many of your symptoms as possible for most accurate results.
- Press themagnifying glass to submit your symptoms.
- You will be able to view and download your results after submitting your symptoms.
- Results include diagnostic profiles of patients with similar symptoms, along with possible disease and/or gene information.
Search symptoms
Type in the symptoms you are experiencing. Need help? We've added some common symptoms below for your reference.
Intellectual disabilityGlobal developmental delaySeizuresGeneralized hypotoniaShort statureSmall head(Microcephaly)Hearing impairmentAbnormal facial shapeCurvature of spine(Scoliosis)
Would you like us to contact your physician?
Our test is a clinical-grade genetic test, which requires a physician's order.
If you are interested in our services and need assistance contacting your physician, please fill out the form below, and we will follow up.
