| Disease | hypersplenism |
| Phenotype | C0037889|hereditary spherocytosis |
| Sentences | 1 |
| 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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