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  2. Von Hippel–Lindau disease - Wikipedia

    en.wikipedia.org/wiki/Von_Hippel–Lindau_disease

    Von Hippel–Lindau disease (VHL), also known as Von Hippel–Lindau syndrome, is a rare genetic disorder with multisystem involvement. [3] It is characterized by visceral cysts and benign tumors with potential for subsequent malignant transformation. It is a type of phakomatosis that results from a mutation in the Von Hippel–Lindau tumor ...

  3. Overview of Von Hippel-Lindau Disease - Healthline

    www.healthline.com/health/von-hippel-lindau-disease

    Because VHL disease can cause tumors in many different parts of the body, not everyone will have the same symptoms. Your symptoms will be dictated by the size of your tumors and where they’re ...

  4. Von Hippel–Lindau tumor suppressor - Wikipedia

    en.wikipedia.org/wiki/Von_Hippel–Lindau_tumor...

    View/Edit Mouse. The Von Hippel–Lindau tumor suppressor also known as pVHL is a protein that, in humans, is encoded by the VHL gene. Mutations of the VHL gene are associated with Von Hippel–Lindau disease, which is characterized by hemangioblastomas of the brain, spinal cord and retina. It is also associated with kidney and pancreatic lesions.

  5. Supreme Hockey League - Wikipedia

    en.wikipedia.org/wiki/Supreme_Hockey_League

    The All-Russian Hockey League (VHL) [1] [2] (Russian: Всероссийская хоккейная лига (ВХЛ), Vserossiyskaya hokkeinaya liga (VHL)), also known as the Major Hockey League [3] [4] or Higher Hockey League (HHL), [5] is a professional ice hockey league in Eurasia, and the second highest level of Russian hockey.

  6. Get Support-AOL Help

    help.aol.com/contact

    Get answers to your AOL Mail, login, Desktop Gold, AOL app, password and subscription questions. Find the support options to contact customer care by email, chat, or phone number.

  7. Phakomatosis - Wikipedia

    en.wikipedia.org/wiki/Phakomatosis

    Von Hippel-Lindau (VHL) disease is an autosomal dominant condition caused by mutations of the VHL gene. [56] Approximately one-in-five cases are de novo rather than familial and it has nearly complete penetrance. [57] VHL occurs in an estimated 1 in 36,000-45,000 live births. [57]

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