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Oncogenetics

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    ACTH-independent macronodular adrenal hyperplasia

    Baller-Gerold syndrome

    Bannayan-Riley-Ruvalcaba syndrome

    BAP1-tumor predisposition syndrome

    Basal cell nevus syndrome

    Bloom syndrome

    Breast and Ovary cancer, hereditary

    Cartilage-hair hypoplasia

    Cowden syndrome

    Desmoplastic medulloblastoma, hereditary

    DICER1 syndrome

    Dyskeratosis congenita

    Gastric cancer

    Hereditary cancer (WES)

    Hereditary melanoma

    Inherited bone marrow failure

    Leiomymatosis + kidney cancer

    Li-Fraumeni syndrome

    Lynch syndrome (HNPCC)

    Mast cell disease

    Melanoma-pancreatic cancer syndrome

    Mismatch repair cancer syndrome

    Multiple endocrine neoplasia type 1 (MEN1)

    Multiple endocrine neoplasia type 2 (MEN2)

    Neurofibromatosis

    Nijmegen breakage syndrome (NBS)

    Pancreatic Cancer

    Paraganglioma and pheochromocytoma, Hereditary

    Pelger Huet anomaly

    Peutz-Jeghers syndrome

    Platelet dysfunction, familial (with AML)

    Polyposis

    Polyposis

    Predictive testing (cancer hotspot panel)

    PTEN Hamartoma Tumor syndrome

    Renal cancer, hereditary

    Renal cell carcinoma

    Rhabdoid tumor predisposition syndrome

    Rothmund-Thomson syndrome

    Schwannomatosis

    Severe combined immunodeficiency

    Somatic overgrowth and vascular malformations

    Sonic Hedgehog medulloblastoma

    Tylosis with esophageal cancer

    Uveal melanoma, hereditary

    Von Hippel-Lindau syndrome

    Werner syndrome

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