SE-ATLAS

Acquired hemophilia Acquired prothrombin deficiency Acquired purpura fulminans Acquired von Willebrand syndrome Alpha delta granule deficiency Alpha granule 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 Alveolar rhabdomyosarcoma Alveolar soft tissue sarcoma Anaplastic ependymoma Anaplastic ganglioglioma Anaplastic oligoastrocytoma Anaplastic oligodendroglioma Anaplastic/large cell medulloblastoma Angiocentric glioma Angiosarcoma Astroblastoma Astrocytoma Atypical papilloma of choroid plexus Atypical teratoid rhabdoid tumor Autoimmune thrombocytopenia Autosomal dominant macrothrombocytopenia Autosomal thrombocytopenia with normal platelets 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 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 Bone sarcoma Central nervous system embryonal tumor Central neurocytoma Cerebellar liponeurocytoma Chondrosarcoma Chordoid glioma Choriocarcinoma of the central nervous system Choroid plexus carcinoma Choroid plexus tumor Classic medulloblastoma Combined deficiency of factor V and factor VIII Congenital alpha2-antiplasmin deficiency Congenital amegakaryocytic thrombocytopenia 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 plasminogen activator inhibitor type 1 deficiency Congenital prekallikrein deficiency Congenital thrombotic thrombocytopenic purpura Congenital vitamin K-dependent coagulation factors deficiency Craniopharyngioma Dedifferentiated liposarcoma Delta-beta-thalassemia Dense granule disease Dermatofibrosarcoma protuberans Desmoplastic infantile astrocytoma/ganglioglioma Desmoplastic small round cell tumor Desmoplastic/nodular medulloblastoma Diffuse leptomeningeal melanocytosis Dominant beta-thalassemia Dysembryoplastic neuroepithelial tumor 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 Extragonadal germ cell tumor Extragonadal germinoma Extragonadal non-dysgerminomatous germ cell tumor Extragonadal teratoma Extraneural perineurioma Extraskeletal Ewing sarcoma Extraskeletal myxoid chondrosarcoma Extraventricular neurocytoma Familial afibrinogenemia Familial dysfibrinogenemia Familial hypodysfibrinogenemia Familial hypofibrinogenemia Familial multiple meningioma Familial thrombocytosis Familial thrombomodulin anomalies Fanconi anemia Fechtner syndrome Fetal and neonatal alloimmune thrombocytopenia Fibrosarcoma Gaisböck syndrome 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 Gonadal germ cell tumor Growing teratoma syndrome Hashimoto-Pritzker syndrome Hb Bart's hydrops fetalis Hemangioblastoma Hemoglobin C-beta-thalassemia syndrome Hemoglobin E-beta-thalassemia syndrome Hemoglobin H disease Hemoglobin Lepore-beta-thalassemia syndrome 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 persistence of fetal hemoglobin-beta-thalassemia syndrome Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome Hereditary thrombocytopenia with normal platelets Hereditary thrombophilia due to congenital antithrombin deficiency Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency High-grade astrocytoma Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency Immune thrombocytopenia Immune-mediated thrombotic thrombocytopenic purpura Intraneural perineurioma Isolated hereditary giant platelet disorder Kaposi sarcoma Langerhans cell histiocytosis specific to childhood Leiomyosarcoma Letterer-Siwe disease Lhermitte-Duclos disease Liposarcoma Low-grade astrocytoma Low-grade ependymoma MYH9-related disease Macrothrombocytopenia with mitral valve insufficiency 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 May-Hegglin thrombocytopenia Mediterranean macrothrombocytopenia Medulloblastoma Medulloblastoma with extensive nodularity Medulloepithelioma of the central nervous system Meningeal melanocytoma Meningioma Mild hemophilia A Mild hemophilia B Mixed germ cell tumor Mixed germ cell tumor of central nervous system Mixed neuronal-glial tumor Moderate hemophilia A Moderate hemophilia B Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome Myxofibrosarcoma Myxoid/round cell liposarcoma Nasal ganglioglioma Nasopharyngeal teratoma Nephroblastoma Neuroblastoma Neuroepithelioma Neurofibroma Neuronal tumor Non-central nervous system-localized embryonal carcinoma Non-seminomatous germ cell tumor of testis Oligoastrocytic tumor Oligoastrocytoma Oligodendroglial tumor Oligodendroglioma Optic pathway glioma Osteosarcoma Ovarian dysgerminoma Painful orbital and systemic neurofibromas-marfanoid habitus syndrome Papillary glioneuronal tumor Papillary tumor of the pineal region Papilloma of choroid plexus Paris-Trousseau thrombocytopenia Perineurioma Peripheral primitive neuroectodermal tumor Pineal parenchymal tumor of intermediate differentiation Pineal tumor of neuroepithelial tissue Pineoblastoma Pineocytoma Pleomorphic liposarcoma Pleomorphic rhabdomyosarcoma Polyembryoma Primary central nervous system lymphoma Primary germ cell tumor of central nervous system Primary melanocytic tumor of central nervous system Primary melanoma of the central nervous system Primary non-gestational choriocarcinoma of ovary Primary oculocerebral lymphoma Protein S acquired deficiency Pseudo-von Willebrand disease Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome Rare coagulation disorder 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 nervous system 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 Reticular perineurioma Rhabdoid tumor Rhabdoid tumor predisposition syndrome Rhabdomyosarcoma Rosette-forming glioneuronal tumor Sclerosing perineurioma Scott syndrome Sebastian syndrome Severe hemophilia A Severe hemophilia B Severe hereditary thrombophilia due to congenital protein C deficiency Severe hereditary thrombophilia due to congenital protein S deficiency 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 Simple cryoglobulinemia Skeletal Ewing sarcoma Soft tissue sarcoma Solitary fibrous tumor Spermatocytic seminoma Stormorken-Sjaastad-Langslet syndrome Syndrome with alpha-thalassemia as a major feature Synovial sarcoma Teratoma of the central nervous system Testicular seminomatous germ cell tumor Thrombocythemia with distal limb defects Thrombocytopenia with congenital dyserythropoietic anemia Thrombocytopenia-absent radius syndrome Thrombotic thrombocytopenic purpura Tumor of cranial and spinal nerves Tumor of meninges Undifferentiated pleomorphic sarcoma Vestibular schwannoma 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 Well-differentiated liposarcoma X-linked dyserythropoietic anemia with abnormal platelets and neutropenia X-linked thrombocytopenia with normal platelets Yolk sac tumor Yolk sac tumor of central nervous system