SE-ATLAS

Syndrome myélodysplasique non-classifié Syndrome de Shwachman-Diamond Anémie hémolytique constitutionnelle rare par anomalie enzymatique Anémie hémolytique auto-immune Hémoglobinopathie Alpha-thalassémie Syndrome de pancytopénie-retard de développement Syndrome de surdité-lymphoedème-leucémie Aplasie médullaire rare Congenital dyserythropoietic anemia type I Congenital dyserythropoietic anemia type III Congenital dyserythropoietic anemia type II Acute myeloid leukaemia with myelodysplasia-related features Fanconi anemia Congenital dyserythropoietic anemia Idiopathic aplastic anemia Primary acquired red cell aplasia Pearson syndrome Acute myeloid leukemia and myelodysplastic syndromes related to alkylating agent Hoyeraal-Hreidarsson syndrome Sickle cell anemia Congenital dyserythropoietic anemia type IV Unclassified myelodysplastic/myeloproliferative disease Monocytopenia with susceptibility to infections Reticular dysgenesis B-lymphoblastic leukemia/lymphoma with t(12;21)(p13.2;q22.1) Craniosynostosis-anal anomalies-porokeratosis syndrome Dyskeratosis congenita Severe congenital neutropenia Acute megakaryoblastic leukemia without Down syndrome Acute myeloid leukemia with t(8;21)(q22;q22) translocation SAMD9L-associated autoinflammatory syndrome Acute myeloid leukemia and myelodysplastic syndromes related to radiation Classic eosinophilic pustular folliculitis Inherited acute myeloid leukemia Chronic myeloid leukemia Polycythemia vera Myeloproliferative neoplasm Essential thrombocythemia