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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
MyVHL: Patient Natural History StudyAbnormalities, Multiple, Ciliopathies, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, angiomatosis, cardiovascular disorder, hereditary disease, hereditary leiomyomatosis and renal cell cancer, hereditary neoplastic syndrome, neoplasm, nervous system disorder, neurocutaneous syndrome, vascular disorder, von Hippel-Lindau diseaseRecruitingNot stated2024-04-26NCT03749980

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Research sitesCityCountryLinked trials
VHL AllianceBostonUnited States1