|
|
Medical Definition of Hippel-lindau disease
1. A syndrome transmitted as an autosomal dominant trait and characterised chiefly by angiomata of the retina and haemangioblastoma of the cerebellum and walls of the fourth ventricle. Ocular complications are often present, as are haemangiomas of the spinal cord, face, and other sites. Symptoms may not be apparent until the third decade in life. (12 Dec 1998)
Lexicographical Neighbors of Hippel-lindau Disease
Other Resources:
