Von Hippel-Lindau Disease is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Von Hippel-Lindau Disease, or a subtype of Von Hippel-Lindau Disease, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Von Hippel-Lindau Disease as a "rare disease".
Source - Orphanet
Genes and Disease:
The following page contains data, researched by the NCBI, identified to have a relationship between certain genes and Von Hippel-Lindau Disease
Bradley, W, et al (eds).
Neurology in Clinical Practice:
Principles of Diagnosis and Management, vol. II Butterworth-Heinemann,
Boston, pp. 1332-1333 (1991)
Joynt, R (ed.)
Clinical Neurology, vol. 3 J.B. Lippincott
Co., Philadelphia, pp. 7, 39, 83 (1992)
Karsdorp, N, et al.
von Hippel-Lindau Disease: New Strategies
in Early Detection and Treatment. The American Journal of Medicine 97;
158-168 (August 1994)
Lesho, E.
Recognition and Management of von Hippel-Lindau
Disease. American Family Physician 50:6; 1269-1272 (November 1, 1994)
Martz, C.
von Hippel-Lindau Disease: A Genetic Condition
Predisposing Tumor Formation. Oncology Nursing Forum 18:3; 545-551 (1991)
(Source: excerpt from NINDS von Hippel-Lindau Disease Information Page: NINDS)
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