Niemann-Pick disease type A

MONDO:0009756

Niemann-Pick disease type A is a very severe subtype of Niemann-Pick disease, an autosomal recessive lysosomal disease, and is characterized clinically by onset in infancy or early childhood with failure to thrive, hepatosplenomegaly, and rapidly progressive neurodegenerative disorders.

Also known as: Niemann-PICK disease, type A, Niemann-Pick disease, Intermediate, protracted neurovisceral, sphingomyelin lipidosis, sphingomyelinase deficiency

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