Embryo Report
Advanced genetic screen for your embryos. Prevent your child from inheriting a predisposition to a condition that runs in your family.
Couple Report
Our preconception test measures your future child's genetic predisposition to disease. Mitigate your risk.
For Patients
Whole genome embryo reports with PGT-M
Screen for known genetic conditions without probes, while also gaining insights on hundreds of additional conditions from whole genome analysis.
Why choose Orchid for PGT-M?
Fast Acceptance
Case acceptance within 24-48 hours
No Probes Required
Simply provide your records to genetics@orchidhealth.com
Screen for More
Screen for hundreds of other conditions. See what is included in our report.
Situations Orchid can help with
Most known genetic conditions
Email genetics@orchidhealth.com and receive case acceptance within 1-2 days.
Challenging conditions that may be rejected elsewhere
For example, cases with multiple variants simultaneously, or small deletions/duplications
Unique clinical scenarios
For example, cases with donors or de novo.
Spinal Muscular Atrophy
Orchid now offers targeted embryo screening for couples at risk for SMA; even in complicated cases, without the need for custom probes or extended family studies. For more information, see our flyer.
Fragile X Syndrome
Direct detection of FMR1 with CGG repeat Numbers, available for known intermediate and permutation carriers. No probes required, so no family member samples required. For more information, see our flyer.
Ready to get started?
Email genetics@orchidhealth.com and receive case acceptance within 1-2 days.
Have healthy babies.
Have healthy babies.
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