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Protocol to guide the assessment of genetic testing for hereditary mutations in the VHL gene that cause von Hippel-Lindau syndrome May 2011 Table of Contents Table of Tables 3
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Document Date: 2014-11-06 23:49:24

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Nordstrom / Adelaide SA / The Cancer Genetics Diagnostic Laboratory / Australian Refined Diagnosis Related Group / /

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glaucoma / highly vascular benign tumours / neoplasms / hereditary mutations / neuroendocrine tumours / headaches / hydrocephalus / headache / facial paresis / VHL syndrome / retinal detachment / cysts / nausea / Renal cell carcinomas / infectious / Pancreatic tumours / leukaemia / numbness / renal cancer / tachycardia / pulmonary embolism / Renal cell carcinoma / hearing loss / clear-cell renal cell carcinoma / papillary cystadenomas / VHL disease / blindness / ataxia / dysmetria / pancreatic cysts / adenocarcinomas / clear cell renal carcinoma / hypertension / cancer / disease / cataracts / neoplasm / disease VHL syndrome / benign neoplasms / congenital disorders / both benign and malignant tumours / venous thrombosis / chronic / Type 2B VHL syndrome / vertigo / tumour / intra-adrenal paragangliomas / Hippel-Lindau syndrome / pancreatitis / angioma / predictionof VHL syndrome / dizziness / cystadenomas / carcinomas / metastases / 2B VHL disease / infectious disease / spinal cord tumours / tinnitus / syndrome / disorders / renal cysts / Tumours / /

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