Genetic Disorder clinical trials
34 active trials name this condition. Describe your situation to see which ones you may be eligible for.
By location
- An Adaptive Clinical Trial of BeginNGS Newborn Screening for Hundreds of Genetic Diseases by Genome Sequencing
- Genomic Uniformed-Screening Against Rare Disease In All Newborns
- Helix Research Network
- Genetic Disorders of Obesity Program Database
- Observational Study of Advanced Data Analytics in Genetic Conditions
- UW Undiagnosed Genetic Diseases Program
- Embryo Health Study
- Follow-up With Preimplantation Genetic Testing Patients
- Diagnostic Odyssey: Whole Genome Sequencing (WGS)
- Amish/Mennonite Research Contact Registry
- Clinical and Molecular Studies in Families With Inherited Eye Disease
- Genetic and Metabolic Disease in Children
- Genetics of Inherited Eye Disease
- Whole Exome and Whole Genome Sequencing for Genotyping of Inherited and Congenital Eye Conditions
- Screening Protocol for Genetic Diseases of Lymphocyte Homeostasis and Programmed Cell Death
- Clinical and Genetic Evaluation of Individuals With Undiagnosed Disorders Through the Undiagnosed Diseases Network
- Studying Childhood-onset Behavioral, Psychiatric, and Developmental Disorders
- Caregiving Networks Across Disease Context and the Life Course
- Inherited Reproductive Disorders
- Rady Children's Institute Genomic Biorepository
- Large Language Models To Improve the Quality of Care of Cardiology Patients
- 4D Duke Microscope Integrated Optical Coherence Tomography in a Zeiss Artevo 800
- UCSF Center for Genome Surgery Biobank and Registry
- The Mayo Clinic Rare and Undiagnosed Disease Hackathon
- Self-Monitoring OCT
- Genome Sequencing in the Intensive Care Unit Population
- Research for Individualized Therapeutics in Rare Genetic Disease
- Economic and Clinical Outcomes of (Whole Exome) Sequencing in Tapestry
- Reverse Phenotyping Core
- Rapid Whole Genome Sequencing Study
- UW ISeqU: Clinical Impact of Whole-genome Sequencing in Adults
- SLC13A5 Deficiency Natural History Study - United States Only
- VIGOR: Virtual Genome Center for Infant Health
- Family Health Histories: Creating a Culturally Tailored Tool to Reduce Health Disparities in the Black Community
Guides for people searching for a trial
- Why people get turned down — and what to do nextWhat eligibility criteria are for, what keeps people out, and where to go when the first door closes.
- How your biomarkers decide which trials you qualify forEGFR, HER2, BRAF, PD-L1 and the rest — what they are and why they increasingly gate access.
- How to search for a trial without losing your mindWhere to look, what to gather first, and how to read what you find.
- What Phase 1, 2 and 3 actually mean for youWhat each phase is testing, and how to weigh an early-phase trial against a later one.
- 10 questions to ask before you say yesTreatment, time, cost, safety and your rights. Worth bringing to a screening visit.
- You matched with a trial. What happens now?Phone screens, the screening visit, informed consent, and day one.
Showing active trials that list “Genetic Disorder” as a condition. Eligibility shown on each trial is an estimate — the trial's study team makes the final decision.