SE-ATLAS

Malignant triton tumor Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome Immune-mediated thrombotic thrombocytopenic purpura Gangliocytoma Familial thrombocytosis Testicular seminomatous germ cell tumor Anaplastic oligoastrocytoma Gaisböck syndrome Acquired prothrombin deficiency Spermatocytic seminoma Sclerosing perineurioma Protein S acquired deficiency Primary oculocerebral lymphoma Reticular perineurioma Germ cell tumor of testis Alpha-thalassemia Intraneural perineurioma Bleeding diathesis due to a collagen receptor defect Glial tumor of neuroepithelial tissue with unknown origin Desmoplastic infantile astrocytoma/ganglioglioma Ependymal tumor Alpha-thalassemia-X-linked intellectual disability syndrome Extraneural perineurioma Beta-thalassemia Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency Rare thrombotic disorder due to a constitutional platelet anomaly Chordoid glioma Dysembryoplastic neuroepithelial tumor Glanzmann thrombasthenia Simple cryoglobulinemia Alveolar soft tissue sarcoma May-Hegglin thrombocytopenia Beta-thalassemia major Letterer-Siwe disease Paris-Trousseau thrombocytopenia Acquired hemophilia Angiocentric glioma Astroblastoma X-linked thrombocytopenia with normal platelets Hashimoto-Pritzker syndrome Fetal and neonatal alloimmune thrombocytopenia Rare thrombotic disorder due to an acquired platelet anomaly Painful orbital and systemic neurofibromas-marfanoid habitus syndrome Primary central nervous system lymphoma Bleeding diathesis due to thromboxane synthesis deficiency Ganglioglioma Extraskeletal Ewing sarcoma Combined deficiency of factor V and factor VIII Craniopharyngioma Angiosarcoma Malignant non-dysgerminomatous germ cell tumor of ovary Hemophilia Macrothrombocytopenia with mitral valve insufficiency Hereditary thrombocytopenia with normal platelets Hepatoblastoma Beta-thalassemia intermedia Meningioma Optic pathway glioma Familial hypodysfibrinogenemia Peripheral primitive neuroectodermal tumor Extragonadal germinoma Bone sarcoma Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16 Essential thrombocythemia Embryonal carcinoma of the central nervous system Isolated hereditary giant platelet disorder Thrombotic thrombocytopenic purpura Dominant beta-thalassemia Congenital amegakaryocytic thrombocytopenia Anaplastic ganglioglioma Epignathus Skeletal Ewing sarcoma Thrombocytopenia-absent radius syndrome Esthesioneuroblastoma Autosomal thrombocytopenia with normal platelets Papillary glioneuronal tumor Rare hereditary thrombophilia Evans syndrome Beta-thalassemia associated with another hemoglobin anomaly Embryonal carcinoma Delta-beta-thalassemia Hemoglobin H disease Familial thrombomodulin anomalies Heparin-induced thrombocytopenia Alpha delta granule deficiency Rare tumor of neuroepithelial tissue Congenital factor II deficiency Alveolar rhabdomyosarcoma Congenital factor V deficiency Congenital factor VII deficiency Congenital factor X deficiency Hemoglobin C-beta-thalassemia syndrome Embryonal rhabdomyosarcoma Congenital plasminogen activator inhibitor type 1 deficiency Acquired purpura fulminans Congenital factor XI deficiency Congenital factor XII deficiency Yolk sac tumor Congenital factor XIII deficiency High-grade astrocytoma Polyembryoma Mixed germ cell tumor Rhabdoid tumor predisposition syndrome Hb Bart's hydrops fetalis Severe hereditary thrombophilia due to congenital protein S deficiency Rosette-forming glioneuronal tumor Rhabdoid tumor Congenital fibrinogen deficiency Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency Severe hereditary thrombophilia due to congenital protein C deficiency Beta-thalassemia with other manifestations Epstein syndrome Extragonadal teratoma Liposarcoma Hemoglobin E-beta-thalassemia syndrome Thrombocythemia with distal limb defects Primary non-gestational choriocarcinoma of ovary Autosomal dominant macrothrombocytopenia Congenital prekallikrein deficiency Stormorken-Sjaastad-Langslet syndrome Leiomyosarcoma Medulloblastoma Non-central nervous system-localized embryonal carcinoma Malignant germ cell tumor of ovary Rare hemorrhagic disorder Bleeding disorder in hemophilia B carriers Ovarian dysgerminoma Congenital high-molecular-weight kininogen deficiency Embryonal tumor of neuroepithelial tissue Fechtner syndrome Bleeding disorder in hemophilia A carriers Beta-thalassemia-X-linked thrombocytopenia syndrome Thrombocytopenia with congenital dyserythropoietic anemia Bleeding disorder due to P2Y12 defect Extragonadal non-dysgerminomatous germ cell tumor Medulloblastoma with extensive nodularity Nasopharyngeal teratoma Benign peripheral nerve sheath tumor Congenital alpha2-antiplasmin deficiency Ganglioneuroma Papilloma of choroid plexus Malignant peripheral nerve sheath tumor with perineurial differentiation Anaplastic/large cell medulloblastoma Solitary fibrous tumor Rare hemorrhagic disorder due to a coagulation factors defect Hereditary thrombophilia due to congenital antithrombin deficiency Alpha-thalassemia-myelodysplastic syndrome Fanconi anemia Primary germ cell tumor of central nervous system Von Willebrand disease Neuroepithelioma Rare hemorrhagic disorder due to a constitutional thrombocytopenia Low-grade astrocytoma Giant cell tumor of bone Gestational choriocarcinoma Desmoplastic/nodular medulloblastoma Nasal ganglioglioma Lhermitte-Duclos disease Rare coagulation disorder Neuroblastoma Growing teratoma syndrome Pleomorphic rhabdomyosarcoma Central nervous system embryonal tumor Von Willebrand disease type 2 Yolk sac tumor of central nervous system Mediterranean macrothrombocytopenia Extragonadal germ cell tumor Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome Von Willebrand disease type 1 Classic medulloblastoma Epithelioid sarcoma Rare hemorrhagic disorder due to a qualitative platelet defect Von Willebrand disease type 2A Astrocytoma Chondrosarcoma Sickle cell anemia Rare hemorrhagic disorder due to a platelet anomaly Hereditary combined deficiency of vitamin K-dependent clotting factors Beta-thalassemia and related diseases Hemoglobin Lepore-beta-thalassemia syndrome Rhabdomyosarcoma Choriocarcinoma of the central nervous system Ganglioneuroblastoma Sickle cell disease and related diseases Von Willebrand disease type 2B Medulloepithelioma of the central nervous system Gonadal germ cell tumor MYH9-related disease Alpha-thalassemia and related disorders Von Willebrand disease type 2N Rare hemorrhagic disorder due to an acquired coagulation factor defect Teratoma of the central nervous system Von Willebrand disease type 2M Ependymoblastoma Rare thrombotic disease of hematologic origin Germinoma of the central nervous system Nephroblastoma Mixed germ cell tumor of central nervous system Von Willebrand disease type 3 Oligodendroglial tumor Primary melanocytic tumor of central nervous system Familial hypofibrinogenemia Benign schwannoma X-linked dyserythropoietic anemia with abnormal platelets and neutropenia Undifferentiated pleomorphic sarcoma Tumor of meninges Choroid plexus tumor Dense granule disease Diffuse leptomeningeal melanocytosis Rare hemorrhagic disorder due to an acquired platelet anomaly Alpha granule disease Sickle cell disease associated with another hemoglobin anomaly Glial tumor Oligodendroglioma Choroid plexus carcinoma Fibrosarcoma Soft tissue sarcoma Severe hemophilia B Osteosarcoma Pineal tumor of neuroepithelial tissue Moderate hemophilia B Sickle cell-beta-thalassemia disease syndrome Scott syndrome Rare thrombotic disorder due to a coagulation factors defect Langerhans cell histiocytosis specific to childhood Sebastian syndrome Anaplastic oligodendroglioma Acquired von Willebrand syndrome Vestibular schwannoma Germ cell tumor Atypical papilloma of choroid plexus Myxoid/round cell liposarcoma Pineoblastoma Severe hemophilia A Atypical teratoid rhabdoid tumor Hemophilia A Rare thrombotic disorder due to a constitutional coagulation factors defect Pleomorphic liposarcoma Mild hemophilia B Perineurioma Low-grade ependymoma Rare nervous system tumor Familial afibrinogenemia Well-differentiated liposarcoma Primary melanoma of the central nervous system Moderate hemophilia A Kaposi sarcoma Hemophilia B Dedifferentiated liposarcoma Pineocytoma Rare thrombotic disorder due to an acquired coagulation factors defect Desmoplastic small round cell tumor Familial dysfibrinogenemia Neurofibroma Sickle cell-hemoglobin C disease syndrome Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation Meningeal melanocytoma Myxofibrosarcoma Hemangioblastoma Synovial sarcoma Bernard-Soulier syndrome Immune thrombocytopenia Sickle cell-hemoglobin D disease syndrome Papillary tumor of the pineal region Bleeding diathesis due to glycoprotein VI deficiency Bleeding diathesis due to integrin alpha2-beta1 deficiency Rare hemorrhagic disorder due to a constitutional coagulation factors defect Rare thrombotic disorder due to a platelet anomaly Mild hemophilia A Sickle cell-hemoglobin E disease syndrome Tumor of cranial and spinal nerves Autoimmune thrombocytopenia Non-seminomatous germ cell tumor of testis Anaplastic ependymoma Rare hemorrhagic disorder due to a constitutional platelet anomaly Pineal parenchymal tumor of intermediate differentiation Extraskeletal myxoid chondrosarcoma Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome Neuronal tumor Oligoastrocytic tumor Malignant peripheral nerve sheath tumor Central neurocytoma Oligoastrocytoma Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome Dermatofibrosarcoma protuberans Syndrome with alpha-thalassemia as a major feature Extraventricular neurocytoma Congenital vitamin K-dependent coagulation factors deficiency East Texas bleeding disorder Mixed neuronal-glial tumor Pseudo-von Willebrand disease Familial multiple meningioma Congenital thrombotic thrombocytopenic purpura Cerebellar liponeurocytoma