About Quoiden
Quoiden combines genealogy and genetics to help families uncover hidden hereditary risks and access lifesaving care — all through a secure, consent-driven platform.
Our Story
Quoiden began with a devastating loss no family should face. When seven-year-old Baine passed away from undiagnosed OTC deficiency, his family searched for answers—uncovering a hidden genetic pattern stretching across generations. Their work with genetic genealogists revealed more than 1,200 relatives potentially at risk, proving that family history can be a powerful tool for uncovering silent health conditions.
Today, Quoiden carries that discovery forward. Built to honor Baine’s memory, our platform helps families privately map their health history, understand their inherited risk, and access no-cost testing and expert guidance. What started as one family’s search for clarity has become a mission to ensure that lifesaving knowledge reaches the people who need it most.
The Story Behind Quoiden
We started Quoiden after losing a loved one to undiagnosed OTC deficiency. That loss drives our mission: to combine genealogy and genetics so families can uncover hidden risk early, access no-cost testing, and get connected to the care that can save lives.
How We're Making a Difference
Free Genetic Screening and Testing
A Platform for Discovery and Care
Connecting Families and Research
Ready to screen for OTC Deficiency?
Begin with our free prescreening to learn if you’re at risk for OTC deficiency. Those who qualify will receive a complimentary at-home genetic test, offering peace of mind and a chance for early intervention.
Frequently Asked Questions
Have questions about Quoiden, OTC deficiency, or rare genetic diseases? Our FAQ provides clear answers and helpful resources to guide you.
What is OTC Deficiency?
OTC deficiency is a genetic condition that affects the body’s ability to break down protein. When protein can’t be processed properly, ammonia builds up in the bloodstream, which can be dangerous - especially for the brain. The good news is that once identified through genetic testing, OTC deficiency can be managed with proper medical care.
What are the symptons of OTC Deficiency?
Symptoms of OTC deficiency can vary from mild to life-threatening. They may include:
* Nausea or vomiting
* Stomach pain
* Headaches
* Extreme tiredness
* Confusion or disorientation
* Trouble waking up
* Coma
In severe cases, untreated OTC deficiency can lead to sudden death.
Who can be affected by OTC Deficiency?
OTC deficiency can affect anyone - babies, children, and adults of any sex. Because the condition is genetic, people can carry the gene without knowing it. Even if no one in your family has been diagnosed, you may still be at risk.
Is testing safe for infants and children?
Yes. Testing for OTC deficiency is non-invasive and completely safe.
If your baby is showing symptoms, testing should be done as soon as possible.
What does Quoiden do?
Quoiden helps families understand their risk of OTC deficiency, connect with doctors, and access genetic testing.
We also support education and clinical research - always with your full consent.
Learn more about what we do here.
Can Quoiden help assess my risk of OTC Deficiency?
Yes! Getting tested for OTC deficiency is simple:
1. Start with a short prescreen questionnaire to see if you may be at risk.
2. If you’re flagged as at risk, you’ll complete a second, more detailed questionnaire to help a doctor determine whether testing is recommended.
3. If you qualify, you may receive free at- home genetic testing.A cheek-swab kit will be mailed to your home with clear, easy-to-follow instructions.
4. Once your sample is processed, a doctor reviews your results and explains the next steps.
Will getting tested affect my health insurance?
No. A federal law called the Genetic Information Nondiscrimination Act (GINA) protects you. It prevents health insurers from using your genetic information to deny coverage or raise your rates.
