Mayo Clinic
This research study is being done to find markers and identify causes of rare and undiagnosed diseases by analyzing patient's DNA (i.e., genetic material), RNA, plasma, urine, tissues, or other samples that could be informative of symptoms. Researchers are creating a biobank (library) of samples and information to learn more about treating rare and undiagnosed diseases.
Inclusion Criteria: * Has Mayo Clinic or other medical health system ID, or another unique identifier * Able to provide informed consent Must meet one of the following: * Individual must have evidence of a rare disease or a suspected genetic disorder as determined by a provider or genetic counselor * Biological family member of an enrolled individual Exclusion Criteria: * Individuals who have situations that would limit compliance with the study requirements * Institutionalized (i.e. Federal Medical Prison)
Patients with rare and undiagnosed disease and their family members may be evaluated on a case by case basis. The research study may perform multi-omics testing to provide a diagnosis or to provide biomarker discovery.
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