Oncogenetics

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

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