Diseases groups
Select the diseases groups of each subnetwork and discover the ERN-EuroBloodNet actions that are devoted to them!
- 1 Red blood cell defects
- 2 Bone marrow failure
- 3 Hemochromatosis and other iron disorders
- 4 Bleeding - Coagulation disorders
- 5 Lymphoid malignancies
- 6 Myeloid malignancies
Red blood cell defects
- Alpha- thalassaemia diseases(Alpha -THAL)
- Beta-thalassemia and related diseases(Beta -THAL)
- Hemoglobinopathy (Other than THAL and SCD)Other than SCD and THAL i.e. HbE disease or HbC disease
- Hereditary elliptocytosis(HE)
- Hereditary spherocytosis(HS)
- Hereditary stomatocytosis(HSt)
- Primary inherited erythrocytosis / Congenital polycythemia( EC/PFCP)
- Rare constitutional hemolytic anemia due to an enzyme disorder (Other than PKD)
- Rare constitutional hemolytic anemia due to pyruvate kinase deficiency(PKD)
- Sickle cell disease and related diseases(SCD)
Bone marrow failure
- Acquired red cell aplasia
- Blackfan-Diamond anemia(BDA)
- Congenital dyserythropoietic anemia(CDA)
- Constitutional megaloblastic anemia
- Dyskeratosis congenita and related disorders(DKC)
- Fanconi anemia(FA)
- GATA2 syndrome
- Paroxysmal nocturnal hemoglobinuria(PNH)
- Rare acquired aplastic anemia (Other than PNH)(AA)
- Rare constitutional aplastic anemia (Other than BDA, DKC, FA, SDS)(CAA)
- Shwachman-Diamond syndrome(SDS)
Hemochromatosis and other iron disorders
- Aceruloplasminemia(ACP)
- Congenital atransferrinemia(CAT)
- Constitutional sideroblastic anemia (excluding Severe congenital hypochromic anemia with ringed sideroblasts)
- Hereditary Hyperferritinemia with or without cataract (OMIM 600886)
- HFE related hereditary hemochromatosis (Symptomatic form of hemochromatosis type 1 - OMIM 235201)
- Iron-refractory iron deficiency anemia syndrome(IRIDA)
- Low iron availability for erythropoiesisIron Refractory Iron deficiency Anemia (IRIDA), Aceruloplasminemia (ACP)
- Microcytic anemia with liver iron overload
- Neuroferritinopathy
- non-HFE related hereditary hemochromatosis(HH types 2A, 2B, 3 and 4A,4B ), TFH1-Related Hemochromatosis (type V), Hereditary Hyperferritinemia Cataract Syndrome
- Porphyrias
- Rare acquired deficiency anemia (Plummer-Vinson syndrome)(PVS)
- Rare defects in iron acquisition and transport:Atransferrinemia, Microcytic anemia with iron loading (DMT1), Sideroblastic anemia (STEAP3)
- Rare hereditary hemochromatosis (Other than Type 1)
Bleeding - Coagulation disorders
- Atypical hemolytic-uremic syndrome
- Hemophilia A(HA)
- Hemophilia B(HB)
- Rare hemorrhagic disease due to constitutional coagulation factors defects (Other than Hemophilia and Von Willebrand disease)
- Rare hemorrhagic disorder due to a constitutional platelet anomaly
- Rare hemorrhagic disorder due to an acquired platelet anomaly
- Rare thrombotic disorder due to a coagulation factors defect
- Rare thrombotic disorder due to quantitative platelet anomaly (High)
- Rare thrombotic disorder due to quantitative platelet anomaly (Low)
- Typical hemolytic-uremic syndrome
- Von Willebrand disease(VWD)
Lymphoid malignancies
- Acute lymphoblastic leukemia
- AL Amyloidosis
- Castleman Disease
- Diffuse large B-cell lymphoma, NOS
- Diffuse large B-cell lymphoma, Other than NOS
- Follicular lymphoma
- Hairy cell leukemia
- Histiocytic Disorders
- Hodgkin lymphoma
- Indolent B-cell lymphomas / Non follicular
- Mantle cell lymphoma
- Mature T-cell neoplasms non primary cutaneous Extra nodal
- Mature T-cell neoplasms non primary cutaneous leukemic
- Mature T-cell neoplasms non primary cutaneous Nodal
- Other agressive B-cell neoplasms
- Plasma cell neoplasm
- Posttransplant lymphoproliferative disorders (PTLD)
- Primary cutaneous lymphoma
Myeloid malignancies
- Acute myeloid leukemia (AML)
- Acute promyelocytic leukemia
- Bloom syndrome
- Chronic myeloid leukemia
- Hypereosinophilic syndrome
- Mastocytosis
- Myelodysplastic syndrome
- Myelodysplastic/myeloproliferative disease
- Myeloid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB or FGFR0
- Myeloid neoplasms with germline predisposition or inherited
- Myeloproliferative neoplasm (Other than Chronic myeloid leukemia and Primary myelofibrosis)
- Secondary polycythemia