Get help finding the cause of an undiagnosed genetic condition
Part of Genetic & congenital clinical trials.
This study evaluates people whose medical cause is still unclear even after genetic tests and other workups. It uses coded health data and lab samples to look for a new or rare genetic cause, and it may return additional (“secondary”) genetic findings.
Summary written for real people, not researchers, by Clin2.
Who can take part
- Your condition is still not diagnosed after thorough medical evaluation, including genetic testing
- You have at least one measurable symptom or test result that could be explained by genetics
- Doctors think your condition may be caused by a gene that hasn’t been identified yet, or by a known gene in a new way
- You (or your guardian) agree to share coded data and store/reuse lab samples for research and future diagnostic use, including outside the program
- You agree to receive extra “secondary findings” from genetic testing
- You can understand the study consent well enough (English proficiency)
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
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