The Mayo Clinic Rare and Undiagnosed Disease Hackathon

Starting soon

Conditions studied: Undiagnosed Diseases, Genetic Diseases, Rare Diseases

In brief

The purpose of this study is to create a Mayo Clinic biospecimen and data repository to support the evaluation of patients with rare and undiagnosed diseases through a structured, multidisciplinary diagnostic program.

Key facts

Study ID

NCT07714161

Run by

Mayo Clinic

People needed

50

Starts

2026-08-01

Expected to finish

2027-08-01

Last updated by the study team

2026-07-20

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients receiving or having received care at Mayo Clinic with rare or undiagnosed conditions; of any age (including pediatric); who can provide informed consent or have a legally authorized representative (LAR).
• Patients who have undergone prior standard genetic testing that was non-diagnostic; and who are nominated by a Mayo Clinic clinician sponsor and selected by the Study Team.

You may not qualify if…

• Patients with a confirmed molecular or clinical diagnosis that fully explains their phenotype
• Patients unable to provide consent and without a legally authorized representative (LAR)
• Patients for whom sample collection cannot be coordinated
• Patients enrolled in a clinical trial that precludes ancillary genomic research (evaluated on a case-by-case basis)
• Prisoners will not be included in this study

Where it is running

• Mayo Clinic — Rochester, Minnesota, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.