Niemann-Pick disease(redirected from Niemann-pick disease, type c)
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Niemann-Pick disease[′nē‚män ′pik di‚zēz]
A hereditary sphingolipidosis due to an enzyme deficiency resulting in abnormal accumulation of sphingomyelin; symptoms include anemia, enlargement of the liver, spleen, and lymph nodes, gastrointestinal disturbances, and various neurologic deficits. Also known as lipid hystiocytosis.
McGraw-Hill Dictionary of Scientific & Technical Terms, 6E, Copyright © 2003 by The McGraw-Hill Companies, Inc.