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PedAM

Pediatric Disease Annotations & Medicines




Disease cholestasis
Phenotype C0017205|gaucher disease
Sentences 1
PubMedID- 24915861 Methods: individuals randomly referred to our outpatient clinics in the past two years for hepatosplenomegaly or isolated splenomegaly, who have been excluded as acid sphingomyelinase deficient npd or gaucher disease, and individuals with newborn cholestasis, psychomotor regression/retardation, were screened for plasma 7-ketocholesterol level.

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