Sphingomyelin lipoidosis is another name of Niemann-Pick disease which refers to a biochemical disorder affecting a lipid (fat) called sphingomyelin which results resulting usually in progre ssive enlargement of the liver and spleen (hepatosplenomegaly), "swollen glands" (lymphadenopathy), anemia and mental and physical deterioration. Niemann-Pick disease is hereditary and follows an autosomal recessive pattern.

Sphingomyelin lipoidosis is also called Sphingomyelinase deficiency. (See Niemann-Pick

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