SE-ATLAS

6-phosphogluconate dehydrogenase deficiency AL amyloidosis Abetalipoproteinemia Aceruloplasminemia Acquired hemophagocytic lymphohistiocytosis associated with malignant disease Acquired hemophilia Acquired idiopathic sideroblastic anemia Acquired prothrombin deficiency Acquired purpura fulminans Acquired von Willebrand syndrome Acute basophilic leukemia Acute biphenotypic leukemia Acute erythroid leukemia Acute leukemia of ambiguous lineage Acute lymphoblastic leukemia Acute megakaryoblastic leukemia Acute monoblastic/monocytic leukemia Acute myeloblastic leukemia with maturation Acute myeloblastic leukemia without maturation Acute myeloid leukaemia with myelodysplasia-related features Acute myeloid leukemia Acute myeloid leukemia and myelodysplastic syndromes related to alkylating agent Acute myeloid leukemia and myelodysplastic syndromes related to radiation Acute myeloid leukemia and myelodysplastic syndromes related to topoisomerase type 2 inhibitor Acute myeloid leukemia with 11q23 abnormalities Acute myeloid leukemia with CEBPA somatic mutations Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22) Acute myeloid leukemia with minimal differentiation Acute myeloid leukemia with recurrent genetic anomaly Acute myeloid leukemia with t(8;16)(p11;p13) translocation Acute myeloid leukemia with t(8;21)(q22;q22) translocation Acute myelomonocytic leukemia Acute panmyelosis with myelofibrosis Acute promyelocytic leukemia Acute undifferentiated leukemia Adamantinoma Adult T-cell leukemia/lymphoma Adult-onset autosomal recessive sideroblastic anemia Aggressive primary cutaneous B-cell lymphoma Aggressive primary cutaneous T-cell lymphoma Aggressive systemic mastocytosis Aleukemic mast cell leukemia Alpha delta granule deficiency Alpha granule disease Alpha-heavy chain disease Alpha-thalassemia Alpha-thalassemia and related disorders Alpha-thalassemia-X-linked intellectual disability syndrome Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16 Alpha-thalassemia-myelodysplastic syndrome Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome Alveolar rhabdomyosarcoma Alveolar soft tissue sarcoma Anaplastic ependymoma Anaplastic ganglioglioma Anaplastic oligoastrocytoma Anaplastic oligodendroglioma Anaplastic/large cell medulloblastoma Angiocentric glioma Angiosarcoma Aregenerative anemia Astroblastoma Astrocytoma Atypical chronic myeloid leukemia Atypical hemolytic uremic syndrome Atypical hemolytic uremic syndrome with B factor anomaly Atypical hemolytic uremic syndrome with C3 anomaly Atypical hemolytic uremic syndrome with H factor anomaly Atypical hemolytic uremic syndrome with I factor anomaly Atypical hemolytic uremic syndrome with MCP/CD46 anomaly Atypical hemolytic uremic syndrome with anti-factor H antibodies Atypical hemolytic uremic syndrome with thrombomodulin anomaly Atypical papilloma of choroid plexus Atypical teratoid rhabdoid tumor Autoimmune hemolytic anemia Autoimmune hemolytic anemia, cold type Autoimmune hemolytic anemia, warm type Autoimmune lymphoproliferative syndrome Autoimmune thrombocytopenia Autosomal dominant aplasia and myelodysplasia Autosomal dominant macrothrombocytopenia Autosomal recessive sideroblastic anemia Autosomal thrombocytopenia with normal platelets B-cell non-Hodgkin lymphoma Benign peripheral nerve sheath tumor Benign schwannoma Bernard-Soulier syndrome Beta-thalassemia Beta-thalassemia and related diseases Beta-thalassemia associated with another hemoglobin anomaly Beta-thalassemia intermedia Beta-thalassemia major Beta-thalassemia with other manifestations Beta-thalassemia-X-linked thrombocytopenia syndrome Bilineal acute leukemia Bleeding diathesis due to a collagen receptor defect Bleeding diathesis due to glycoprotein VI deficiency Bleeding diathesis due to integrin alpha2-beta1 deficiency Bleeding diathesis due to thromboxane synthesis deficiency Bleeding disorder due to P2Y12 defect Bleeding disorder in hemophilia A carriers Bleeding disorder in hemophilia B carriers Bloom syndrome Bone sarcoma Bullous diffuse cutaneous mastocytosis Central nervous system embryonal tumor Central neurocytoma Cerebellar liponeurocytoma Chondrosarcoma Chordoid glioma Choriocarcinoma of the central nervous system Choroid plexus carcinoma Choroid plexus tumor Chronic eosinophilic leukemia Chronic myeloid leukemia Chronic myelomonocytic leukemia Chronic myeloproliferative disease, unclassifiable Chronic neutrophilic leukemia Chédiak-Higashi syndrome Classic Hodgkin lymphoma Classic mast cell leukemia Classic medulloblastoma Cold agglutinin disease Combined deficiency of factor V and factor VIII Combined immunodeficiency due to CD27 deficiency Composite lymphoma Congenital alpha2-antiplasmin deficiency Congenital amegakaryocytic thrombocytopenia Congenital atransferrinemia Congenital dyserythropoietic anemia Congenital dyserythropoietic anemia type I Congenital dyserythropoietic anemia type II Congenital dyserythropoietic anemia type III Congenital dyserythropoietic anemia type IV Congenital epulis Congenital erythropoietic porphyria Congenital factor II deficiency Congenital factor V deficiency Congenital factor VII deficiency Congenital factor X deficiency Congenital factor XI deficiency Congenital factor XII deficiency Congenital factor XIII deficiency Congenital fibrinogen deficiency Congenital high-molecular-weight kininogen deficiency Congenital intrinsic factor deficiency Congenital plasminogen activator inhibitor type 1 deficiency Congenital prekallikrein deficiency Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome Congenital thrombotic thrombocytopenic purpura Congenital vitamin K-dependent coagulation factors deficiency Constitutional anemia due to iron metabolism disorder Constitutional deficiency anemia Constitutional dyserythropoietic anemia Constitutional hemolytic anemia due to acanthocytosis Constitutional megaloblastic anemia due to folate metabolism disorder Constitutional megaloblastic anemia due to vitamin B12 metabolism disorder Constitutional megaloblastic anemia with severe neurologic disease Constitutional sideroblastic anemia Craniopharyngioma Cutaneous mastocytoma Cutaneous mastocytosis Deafness-lymphedema-leukemia syndrome Dedifferentiated liposarcoma Dehydrated hereditary stomatocytosis Delta-beta-thalassemia Dendritic cell sarcoma not otherwise specified Dendritic cell tumor Dense granule disease Dermatofibrosarcoma protuberans Desmoid tumor Desmoplastic infantile astrocytoma/ganglioglioma Desmoplastic small round cell tumor Desmoplastic/nodular medulloblastoma Diamond-Blackfan anemia Diaphyseal medullary stenosis-bone malignancy syndrome Diffuse cutaneous mastocytosis Diffuse leptomeningeal melanocytosis Dominant beta-thalassemia Drug-induced autoimmune hemolytic anemia Dysembryoplastic neuroepithelial tumor Dyskeratosis congenita East Texas bleeding disorder Embryonal carcinoma Embryonal carcinoma of the central nervous system Embryonal rhabdomyosarcoma Embryonal tumor of neuroepithelial tissue Ependymal tumor Ependymoblastoma Epignathus Epithelioid sarcoma Epstein syndrome Essential thrombocythemia Esthesioneuroblastoma Evans syndrome Extracutaneous mastocytoma Extragonadal germ cell tumor Extragonadal germinoma Extragonadal non-dysgerminomatous germ cell tumor Extragonadal teratoma Extramedullary soft tissue plasmacytoma Extraneural perineurioma Extranodal nasal NK/T cell lymphoma Extraskeletal Ewing sarcoma Extraskeletal myxoid chondrosarcoma Extraventricular neurocytoma Familial LCAT deficiency Familial afibrinogenemia Familial dysfibrinogenemia Familial hemophagocytic lymphohistiocytosis Familial hypodysfibrinogenemia Familial hypofibrinogenemia Familial multiple meningioma Familial pseudohyperkalemia Familial thrombocytosis Familial thrombomodulin anomalies Fanconi anemia Fechtner syndrome Fetal and neonatal alloimmune thrombocytopenia Fibrosarcoma Follicular dendritic cell sarcoma Formiminoglutamic aciduria Gaisböck syndrome Gamma-heavy chain disease Gangliocytoma Ganglioglioma Ganglioneuroblastoma Ganglioneuroma Germ cell tumor Germ cell tumor of testis Germinoma of the central nervous system Gestational choriocarcinoma Giant cell tumor of bone Glanzmann thrombasthenia Glial tumor Glial tumor of neuroepithelial tissue with unknown origin Glomus tumor Glutamate-cysteine ligase deficiency Glutathione synthetase deficiency Glutathione synthetase deficiency with 5-oxoprolinuria Glutathione synthetase deficiency without 5-oxoprolinuria Glycogen storage disease due to aldolase A deficiency Glycogen storage disease due to muscle phosphofructokinase deficiency Glycogen storage disease due to phosphoglycerate kinase 1 deficiency Gonadal germ cell tumor Griscelli syndrome type 2 Growing teratoma syndrome Hashimoto-Pritzker syndrome Hb Bart's hydrops fetalis Heavy chain deposition disease Heavy chain disease Heinz body anemia Hemangioblastoma Hemoglobin C disease Hemoglobin C-beta-thalassemia syndrome Hemoglobin D disease Hemoglobin E disease Hemoglobin E-beta-thalassemia syndrome Hemoglobin H disease Hemoglobin Lepore-beta-thalassemia syndrome Hemoglobin M disease Hemoglobinopathy Hemoglobinopathy Toms River Hemolytic anemia due to a disorder of glycolytic enzymes Hemolytic anemia due to adenylate kinase deficiency Hemolytic anemia due to an erythrocyte nucleotide metabolism disorder Hemolytic anemia due to diphosphoglycerate mutase deficiency Hemolytic anemia due to erythrocyte adenosine deaminase overproduction Hemolytic anemia due to glucophosphate isomerase deficiency Hemolytic anemia due to glutathione reductase deficiency Hemolytic anemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency Hemolytic anemia due to hexose monophosphate shunt and glutathione metabolism anomalies Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency Hemolytic anemia due to red cell pyruvate kinase deficiency Hemolytic disease due to fetomaternal alloimmunization Hemolytic disease of the newborn with Kell alloimmunization Hemolytic uremic syndrome with DGKE deficiency Hemophagocytic syndrome Hemophagocytic syndrome associated with an infection Hemophilia Hemophilia A Hemophilia B Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation Heparin-induced thrombocytopenia Hepatoblastoma Hereditary combined deficiency of vitamin K-dependent clotting factors Hereditary cryohydrocytosis with reduced stomatin Hereditary elliptocytosis Hereditary folate malabsorption Hereditary isolated aplastic anemia Hereditary methemoglobinemia Hereditary orotic aciduria Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome Hereditary spherocytosis Hereditary stomatocytosis Hereditary thrombocytopenia with normal platelets Hereditary thrombophilia due to congenital antithrombin deficiency Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency Hermansky-Pudlak syndrome due to AP-3 deficiency High-grade astrocytoma Histiocytic and dendritic cell tumor Histiocytic sarcoma Hodgkin lymphoma Homocystinuria without methylmalonic aciduria Hoyeraal-Hreidarsson syndrome Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency Hypereosinophilic syndrome Hypoxanthine guanine phosphoribosyltransferase partial deficiency Hypoxanthine-guanine phosphoribosyltransferase deficiency IRIDA syndrome Idiopathic aplastic anemia Idiopathic hypereosinophilic syndrome Imerslund-Gräsbeck syndrome Immune thrombocytopenia Immune-mediated thrombotic thrombocytopenic purpura Immunodeficiency syndrome with hypopigmentation Immunodeficiency-associated lymphoproliferative disease Indolent primary cutaneous B-cell lymphoma Indolent primary cutaneous T-cell lymphoma Indolent systemic mastocytosis Infantile myofibromatosis Inflammatory myofibroblastic tumor Inherited acute myeloid leukemia Interdigitating dendritic cell sarcoma Intraneural perineurioma Isolated bone marrow mastocytosis Isolated hereditary giant platelet disorder Juvenile hyaline fibromatosis Juvenile myelomonocytic leukemia Kaposi sarcoma Kaposiform hemangioendothelioma Langerhans cell histiocytosis Langerhans cell histiocytosis specific to childhood Langerhans cell sarcoma Leiomyosarcoma Lesch-Nyhan syndrome Lethal hemolytic anemia-genital anomalies syndrome Letterer-Siwe disease Lhermitte-Duclos disease Light and heavy chain deposition disease Light chain deposition disease Lipoblastoma Liposarcoma Low-grade astrocytoma Low-grade ependymoma Lymphoadenopathic mastocytosis with eosinophilia Lymphoid hemopathy Lymphoma Lymphoproliferative disease associated with primary immune disease MYH9-related disease Macrophage activation syndrome Macrophage or histiocytic tumor Macrothrombocytopenia with mitral valve insufficiency Maculopapular cutaneous mastocytosis Maffucci syndrome Malignant germ cell tumor of ovary Malignant non-dysgerminomatous germ cell tumor of ovary Malignant peripheral nerve sheath tumor Malignant peripheral nerve sheath tumor with perineurial differentiation Malignant triton tumor Mast cell leukemia Mast cell sarcoma Mastocytosis May-Hegglin thrombocytopenia McLeod neuroacanthocytosis syndrome Mediterranean macrothrombocytopenia Medulloblastoma Medulloblastoma with extensive nodularity Medulloepithelioma of the central nervous system Melanoma of soft tissue Meningeal melanocytoma Meningioma Methotrexate-associated lymphoproliferative disorders Methylcobalamin deficiency type cblDv1 Methylcobalamin deficiency type cblE Methylcobalamin deficiency type cblG Methylmalonic acidemia with homocystinuria Methylmalonic acidemia with homocystinuria type cblF Methylmalonic acidemia with homocystinuria, type cblC Methylmalonic acidemia with homocystinuria, type cblD Methylmalonic acidemia with homocystinuria, type cblJ Methylmalonic acidemia with homocystinuria, type cblX Microcytic anemia with liver iron overload Mild hemophilia A Mild hemophilia B Mitochondrial myopathy and sideroblastic anemia Mixed germ cell tumor Mixed germ cell tumor of central nervous system Mixed neuronal-glial tumor Mixed-type autoimmune hemolytic anemia Moderate hemophilia A Moderate hemophilia B Mu-heavy chain disease Multiple myeloma Multiple osteochondromas Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome Mycosis fungoides and variants Myelodysplastic syndrome Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality Myelodysplastic/myeloproliferative disease Myeloid hemopathy Myeloid sarcoma Myeloid/lymphoid neoplasm associated with FGFR1 rearrangement Myeloid/lymphoid neoplasm associated with PDGFRA rearrangement Myeloid/lymphoid neoplasm associated with PDGFRB rearrangement Myeloid/lymphoid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB, FGFR1 or JAK2 Myeloproliferative neoplasm Myxofibrosarcoma Myxoid/round cell liposarcoma Nasal ganglioglioma Nasopharyngeal teratoma Nephroblastoma Neuroblastoma Neuroepithelioma Neurofibroma Neuronal tumor Nodular lymphocyte predominant Hodgkin lymphoma Nodular urticaria pigmentosa Non-Hodgkin lymphoma Non-Langerhans cell histiocytosis Non-amyloid monoclonal immunoglobulin deposition disease Non-central nervous system-localized embryonal carcinoma Non-seminomatous germ cell tumor of testis Non-spherocytic hemolytic anemia due to hexokinase deficiency OSLAM syndrome Oligoastrocytic tumor Oligoastrocytoma Oligodendroglial tumor Oligodendroglioma Ollier disease Optic pathway glioma Osteoblastoma Osteosarcoma Ovarian dysgerminoma Overhydrated hereditary stomatocytosis POEMS syndrome Painful orbital and systemic neurofibromas-marfanoid habitus syndrome Pancreatic insufficiency-anemia-hyperostosis syndrome Papillary glioneuronal tumor Papillary tumor of the pineal region Papilloma of choroid plexus Paris-Trousseau thrombocytopenia Paroxysmal cold hemoglobinuria Paroxysmal nocturnal hemoglobinuria Pearson syndrome Perineurioma Peripheral primitive neuroectodermal tumor Persistent polyclonal B-cell lymphocytosis Pineal parenchymal tumor of intermediate differentiation Pineal tumor of neuroepithelial tissue Pineoblastoma Pineocytoma Plaque-form urticaria pigmentosa Plasma cell tumor Plasmacytoma Pleomorphic liposarcoma Pleomorphic rhabdomyosarcoma Plummer-Vinson syndrome Polycythemia vera Polyembryoma Post-transplant lymphoproliferative disease Primary CD59 deficiency Primary acquired pure red cell aplasia Primary acquired red cell aplasia Primary bone lymphoma Primary central nervous system lymphoma Primary cutaneous B-cell lymphoma Primary cutaneous CD30+ T-cell lymphoproliferative disease Primary cutaneous CD4+ small/medium-sized pleomorphic T-cell lymphoma Primary cutaneous T-cell lymphoma Primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma Primary cutaneous diffuse large B-cell lymphoma, leg type Primary cutaneous follicle center lymphoma Primary cutaneous gamma/delta-positive T-cell lymphoma Primary cutaneous lymphoma Primary cutaneous marginal zone B-cell lymphoma Primary cutaneous peripheral T-cell lymphoma not otherwise specified Primary germ cell tumor of central nervous system Primary hemophagocytic lymphohistiocytosis Primary hypereosinophilic syndrome Primary intraocular lymphoma Primary localized amyloidosis Primary lymphoma of the conjunctiva Primary melanocytic tumor of central nervous system Primary melanoma of the central nervous system Primary myelofibrosis Primary non-gestational choriocarcinoma of ovary Primary oculocerebral lymphoma Primary organ-specific lymphoma Primary plasmacytoma of the bone Primary pulmonary lymphoma Primary systemic amyloidosis Protein S acquired deficiency Pseudo-von Willebrand disease Pseudoxanthomatous diffuse cutaneous mastocytosis Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome Rare acquired aplastic anemia Rare acquired deficiency anemia Rare acquired hemolytic anemia Rare anemia Rare aplastic anemia Rare bone tumor Rare coagulation disorder Rare constitutional aplastic anemia Rare constitutional hemolytic anemia Rare constitutional hemolytic anemia due to a red cell membrane anomaly Rare constitutional hemolytic anemia due to an enzyme disorder Rare deficiency anemia Rare hemolytic anemia Rare hemorrhagic disorder Rare hemorrhagic disorder due to a coagulation factors defect Rare hemorrhagic disorder due to a constitutional coagulation factors defect Rare hemorrhagic disorder due to a constitutional platelet anomaly Rare hemorrhagic disorder due to a constitutional thrombocytopenia Rare hemorrhagic disorder due to a platelet anomaly Rare hemorrhagic disorder due to a qualitative platelet defect Rare hemorrhagic disorder due to an acquired coagulation factor defect Rare hemorrhagic disorder due to an acquired platelet anomaly Rare hereditary thrombophilia Rare immune disease Rare nervous system tumor Rare soft tissue tumor Rare thrombotic disease of hematologic origin Rare thrombotic disorder due to a coagulation factors defect Rare thrombotic disorder due to a constitutional coagulation factors defect Rare thrombotic disorder due to a constitutional platelet anomaly Rare thrombotic disorder due to a platelet anomaly Rare thrombotic disorder due to an acquired coagulation factors defect Rare thrombotic disorder due to an acquired platelet anomaly Rare tumor of neuroepithelial tissue Refractory anemia Refractory anemia with excess blasts Refractory anemia with excess blasts in transformation Refractory anemia with excess blasts type 1 Refractory anemia with excess blasts type 2 Refractory cytopenia with multilineage dysplasia Reticular perineurioma Revesz syndrome Rh deficiency syndrome Rhabdoid tumor Rhabdoid tumor predisposition syndrome Rhabdomyosarcoma Rosette-forming glioneuronal tumor Sclerosing perineurioma Scott syndrome Sebastian syndrome Secondary hemophagocytic lymphohistiocytosis Secondary hypereosinophilic syndrome Severe congenital hypochromic anemia with ringed sideroblasts Severe hemophilia A Severe hemophilia B Severe hereditary thrombophilia due to congenital protein C deficiency Severe hereditary thrombophilia due to congenital protein S deficiency Shiga toxin-associated hemolytic uremic syndrome Shwachman-Diamond syndrome Sickle cell anemia Sickle cell disease and related diseases Sickle cell disease associated with another hemoglobin anomaly Sickle cell-beta-thalassemia disease syndrome Sickle cell-hemoglobin C disease syndrome Sickle cell-hemoglobin D disease syndrome Sickle cell-hemoglobin E disease syndrome Sideroblastic anemia Simple cryoglobulinemia Skeletal Ewing sarcoma Smoldering systemic mastocytosis Soft tissue sarcoma Solitary fibrous tumor Southeast Asian ovalocytosis Spermatocytic seminoma Stormorken-Sjaastad-Langslet syndrome Subcutaneous panniculitis-like T-cell lymphoma Syndrome with alpha-thalassemia as a major feature Synovial sarcoma Systemic mastocytosis Systemic mastocytosis with associated hematologic neoplasm Sézary syndrome T-cell non-Hodgkin lymphoma Telangiectasia macularis eruptiva perstans Teratoma of the central nervous system Testicular seminomatous germ cell tumor Therapy related acute myeloid leukemia and myelodysplastic syndrome Thiamine-responsive megaloblastic anemia syndrome Thrombocythemia with distal limb defects Thrombocytopenia with congenital dyserythropoietic anemia Thrombocytopenia-absent radius syndrome Thrombotic thrombocytopenic purpura Thyroid lymphoma Transcobalamin deficiency Transient erythroblastopenia of childhood Tricuspid atresia Triose phosphate-isomerase deficiency Tumor of cranial and spinal nerves Tumor of hematopoietic and lymphoid tissues Tumor of meninges Typical urticaria pigmentosa Unclassified acute myeloid leukemia Unclassified myelodysplastic syndrome Unclassified myelodysplastic/myeloproliferative disease Undifferentiated pleomorphic sarcoma Unstable hemoglobin disease Vestibular schwannoma Vitamin B12- and folate-independent constitutional megaloblastic anemia Von Willebrand disease Von Willebrand disease type 1 Von Willebrand disease type 2 Von Willebrand disease type 2A Von Willebrand disease type 2B Von Willebrand disease type 2M Von Willebrand disease type 2N Von Willebrand disease type 3 WT limb-blood syndrome Well-differentiated liposarcoma X-linked dyserythropoietic anemia with abnormal platelets and neutropenia X-linked lymphoproliferative disease X-linked sideroblastic anemia X-linked sideroblastic anemia and spinocerebellar ataxia X-linked thrombocytopenia with normal platelets Yolk sac tumor Yolk sac tumor of central nervous system