Category:Von Hippel-Lindau disease

**von Hippel-Lindau disease**
	a rare genetic disorder characterized by visceral cysts and benign tumors in multiple organ systems with potential for subsequent malignant change.
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Instance of	head and neck disease; developmental defect during embryogenesis; rare disease; class of disease;
Subclass of	hemangioblastoma; multiple polyglandular tumor; syndromic developmental defect of the eye; inherited nervous system cancer-predisposing syndrome; genetic central nervous system and retinal vascular disease; inherited renal tumor; hereditary eye tumor; central nervous system and retinal vascular disease; catecholamine-producing tumor; familial cystic renal disease; malformation syndrome with hamartosis; syndromic glaucoma; disease;
Named after	Arvid Lindau;
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	Q741315;
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