Disease | hemolytic anemia |
Phenotype | C0024790|paroxysmal nocturnal hemoglobinuria |
Sentences | 3 |
PubMedID- 24369265 | [autoimmune hemolytic anemia with a paroxysmal nocturnal hemoglobinuria-like defect: report of one case]. |
PubMedID- 26043387 | paroxysmal nocturnal hemoglobinuria is manifests with a chronic hemolytic anemia from uncontrolled complement activation, a propensity for thrombosis and marrow failure. |
PubMedID- 22851928 | In the present, replacement therapy of c1-inhibitor is also another established treatment for hereditary angioedema in addition to anti-c5 antibodies for c-dependent hemolytic anemia in patients with paroxysmal nocturnal hemoglobinuria, respectively [155,156]. |
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