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PedAM

Pediatric Disease Annotations & Medicines




Disease hypersplenism
Phenotype C0037889|hereditary spherocytosis
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PubMedID- 25538966 Common indications of pse include hypersplenism with portal hypertension, hereditary spherocytosis, thalassemia, autoimmune hemolytic anemia, splenic trauma, idiopathic thrombocytopenic purpura, splenic hemangioma, and liver cancer.

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