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Review Question - QID 213239

Von Hippel-Lindau Disease Introduction Autosomal dominant syndrome secondary to VHL gene mutation on chromosome 3 QID: 213239 (M1.OMB.19.1)
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QID 213239 (Type "213239" in App Search)
A 23-year-old man presents to his primary care physician with 2 weeks of headache, palpitations, and excessive sweating. He has no past medical history and his family history is significant for clear cell renal cell carcinoma in his father as well as retinal hemangioblastomas in his older sister. On presentation his temperature is 99°F (37.2°C), blood pressure is 181/124 mmHg, pulse is 105/min, and respirations are 18/min. After administration of appropriate medications, he is taken emergently for surgical removal of a mass that was detected by abdominal computed tomography scan. A mutation on which of the following chromosomes would most likely be seen in this patient?
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