SE-ATLAS

Triton-Tumor, maligner Hereditäre Persistenz des fetalen Hämoglobins - beta-Thalassämie Thrombotisch-thrombozytopenische Purpura, immun-vermittelte Gangliozytom Thrombozytose, familiäre Testikulärer Keimzelltumor, seminomatöser Oligoastrozytom, anaplastisches Gaisböck-Syndrom Faktor II-Mangel, erworbener Seminom, spermatozytisches Perineuriom, sklerosierendes Protein-S-Mangel, erworbener Lymphom, okulozerebrales primäres Perineuriom, retikuläres Keimzelltumor, testikulärer Alpha-Thalassämie Perineuriom, intraneurales Hämorrhagische Diathese durch Kollagen-Rezeptor-Mangel Gliom des neuroepithelialen Gewebes mit unbekannter Ursache Astrozytom/Gangliogliom, desmoplastisches, infantiles Tumor, ependymaler Alpha-Thalassämie-X-chromosomale Intelligenzminderung-Syndrom Perineuriom, extraneurales Beta-Thalassämie Hyperkoagulabilitätssyndrom durch Glykosylphosphatidyl-Inositol-Mangel Seltene thrombotische Störung durch konstitutionelle Blutplättchenanomalie Chordoidgliom Tumor, dysembryoplastischer neuroepithelialer Thrombasthenie Glanzmann Kryoglobulinämie, einfache Weichteilsarkom, alveoläres Thrombozytopenie May-Hegglin Beta-Thalassämie major Letterer-Siwe-Krankheit Paris-Trousseau-Syndrom Hämophilie, erworbene Gliom, angiozentrisches Astroblastom Thrombozytopenie, X-chromosomale, mit normalen Plättchen Hashimoto-Pritzker-Syndrom Alloimmunthrombozytopenie, fetale und neonatale Seltene thrombotische Störung durch erworbene Blutplättchenanomalie Schmerzhafte orbitale und systemische Neurofibrome-marfanoider Habitus-Syndrom Primäres Lymphom des Zentralnervensystems Hämorrhagische Diathese durch Thromboxan-Synthetase-Mangel Gangliogliom Extraskelettales Ewing-Sarkom Kombinierter Mangel an Faktor V und Faktor VIII Kraniopharyngeom Angiosarkom Keimzelltumor des Ovars, nicht-dysgerminomatöser maligner Hämophilie Makrothrombozytopenie mit Mitralklappeninsuffizienz Thrombozytopenie, hereditäre, mit normalen Plättchen Hepatoblastom Beta-Thalassämie intermedia Meningeom Optikusgliom Hypodysfibrinogenämie, familiäre Peripherer primitiver neuroektodermaler Tumor Germinom, extragonadales Knochensarkom Alpha-Thalassämie-Intelligenzminderung-Syndrom, gekoppelt an Chr. 16 Essentielle Thrombozythämie Embryonalkarzinom des Zentralnervensystems Giant-Platelet-Syndrom, isoliertes hereditäres Purpura, thrombotische thrombozytopenische Beta-Thalassämie, dominante Angeborene amegakaryozytäre Thrombozytopenie Gangliogliom, anaplastisches Epignathus Ewing-Sarkom, skelettales Thrombozytopenie-Radiusaplasie-Syndrom Ästhesioneuroblastom Thrombozytopenie mit normalen Plättchen, autosomale Form Tumor, glioneuraler papillärer Thrombophilie, hereditäre, seltene Evans-Syndrom Beta-Thalassämie mit assoziierter sonstiger Hämoglobin-Anomalie Embryonales Karzinom Delta-beta-Thalassämie Hämoglobin-H-Krankheit Thrombomodulin-Anomalie, genetisch bedingte Thrombozytopenie, Heparin-induzierte Alpha- und Delta-Thrombozytengranula-Mangel Seltener Tumor des neuroepithelialen Gewebes Faktor II-Mangel, kongenitaler Rhabdomyosarkom, alveoläres Faktor V-Mangel, kongenitaler Faktor VII-Mangel, kongenitaler Faktor X-Mangel, kongenitaler Hämoglobin C - Beta-Thalassämie Rhabdomyosarkom, embryonales Plasminogenaktivator-Inhibitor Typ 1-Mangel, kongenitaler 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