genetic
Von Hippel–Lindau disease
Von Hippel–Lindau disease (VHL), also known as Von Hippel–Lindau , is a rare disorder with multisystem involvement. It is characterized by polycystic disease and with potential for subsequent transformation. It is a type of phakomatosis that results from a in the Von Hippel–Lindau tumor suppressor gene on 3p25.3.
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