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PedAM

Pediatric Disease Annotations & Medicines




Disease thrombocytosis
Phenotype C0024790|paroxysmal nocturnal hemoglobinuria
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PubMedID- 22192057 paroxysmal nocturnal hemoglobinuria-myelodysplastic syndrome associated with marked thrombocytosis and acquired clonal cytogenetic abnormality of t(3;12)(q28;q15).

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