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Up to: Hereditary neurological disease · Autosomal dominant disease · Neurocutaneous syndrome
Von Hippel-Lindau disease
An autosomal dominant disorder caused by pathogenic variants in the VHL gene, leading to an increased risk of various benign and malignant tumors, including hemangioblastomas, retinal hemangiomas, endolymphatic sac tumors, renal cell carcinoma, and pheochromocytomas.
This condition has no sub-types.