PedAM
Pediatric Disease Annotations & Medicines
| Disease | thrombocytosis |
| Phenotype | C0019048|hemoglobinuria |
| Sentences | 1 |
| 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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