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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Frequency and Clinical Phenotype of BAP1 Hereditary Predisposition SyndromeDigestive System Diseases, Digestive System Neoplasms, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Liver Neoplasms, Male Urogenital Diseases, Neoplasms by Histologic Type, Neoplasms by Site, Neoplasms, Germ Cell and Embryonal, Neoplasms, Nerve Tissue, Skin and Connective Tissue Diseases, Urogenital Diseases, Urogenital Neoplasms, Uveal Neoplasms, adenocarcinoma, adenoma, benign urinary system neoplasm, carcinoma, cholangiocarcinoma, cutaneous melanoma, epithelial neoplasm, eye disorder, hepatocellular carcinoma, kidney cancer, kidney disorder, liver disorder, melanocytic neoplasm, melanoma, mesothelial neoplasm, mesothelioma, neoplasm, neuroendocrine neoplasm, ocular cancer, primitive neuroectodermal tumor, renal cell carcinoma, skin disorder, skin neoplasm, urinary system disorder, uveal disorder, uveal melanomaRecruitingNot stated2026-03-09NCT04792463