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PedAM

Pediatric Disease Annotations & Medicines




Disease lysosomal storage disease
Phenotype C0037899|sphingolipidoses
Sentences 1
PubMedID- 24607565 The sphingolipidoses are a group of inherited lysosomal storage diseases in which sphingolipids accumulate due to the defective activity of one or other enzymes involved in their degradation.

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