Genome surgery biobank and registry study
Part of Genetic & congenital clinical trials.
This study collects information and samples from people with genetic conditions to help researchers learn more and develop new treatments. You can participate even if you are pregnant, a child, or a family member of someone with a genetic condition.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You have a condition that is genetic or might be genetic
- You are a patient at UCSF or you agree to have your case discussed by a team of experts
- You can join even if you are a child, pregnant, or a family member of someone in the study
- You must give permission (informed consent) to be in the registry and biobank part
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
Similar studies
Other trials that look related to this one.
This is an observational study that collects health and family history information to see how advanced data analysis can help people with genetic conditions. It may involve website forms, optional conversations, and sometimes an NIH visit, depending on your situation.
This study collects and stores DNA samples and related health information from people of all ages. It helps researchers understand childhood diseases better and may support future discoveries and treatments.
This study builds a large DNA and health information “biobank” from adults who visit Intermountain Health. It may help researchers understand how genes relate to health and disease by comparing “healthy” people with people who have medical conditions.
This study quickly reads a child’s DNA using whole genome sequencing to look for genetic causes of symptoms. It may help families and doctors better understand an underlying genetic condition and guide medical care.
This registry collects past and ongoing health and genetic testing information from adults who have had germline or other genetic/blood biomarker tests. It helps researchers learn patterns that may improve cancer care in the future.
This study uses advanced gene sequencing to look for the genetic cause of rare diseases that haven't been explained yet. You or a family member might join to help find a diagnosis and contribute to medical research.
Hear when a new Any Conditions That Are Genetic or Suspected to be Genetic in Origin trial opens
We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.