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-Syndrom Typ 1 Medulloblastom, klassisches Epitheloidsarkom Seltene Blutgerinnungsstörung durch qualitativen Plättchen-Defekt Von-Willebrand-Syndrom Typ 2A Astrozytom Chondrosarkom Sichelzellanämie Seltene Blutgerinnungsstörung durch Blutplättchenanomalie Vitamin K-abhängige Gerinnungsfaktoren, hereditärer kombinierter Mangel Beta-Thalassämie und verwandte Krankheiten Hämoglobin Lepore-Beta-Thalassämie-Syndrom Rhabdomyosarkom Chorionkarzinom des Zentralnervensystems Ganglioneuroblastom Sichelzellkrankheit und verwandte Störungen Von-Willebrand-Syndrom Typ 2B Medulloepitheliom des Zentralnervensystems Keimzelltumor, gonadaler MYH9-assoziierte Krankheiten Alpha-Thalassämie und verwandte Krankheiten Von-Willebrand-Syndrom Typ 2N Blutgerinnungsstörung, erworbene Teratom des Zentralnervensystems Von-Willebrand-Syndrom Typ 2M Ependymoblastom Thrombotische Krankheit hämatologischen Ursprungs, seltene Germinom des Zentralnervensystems Nephroblastom Gemischter Keimzelltumor des Zentralnervensystems Von-Willebrand-Syndrom Typ 3 Oligodendroglialer Tumor Primärer melanozytärer Tumor des Zentralnervensystems Hypofibrinogenämie, familiäre Schwannom, benignes X-chromosomale dyserythropoetische Anämie mit abnormen Blutplättchen und Neutropenie Sarkom, undifferenziertes pleomorphes Tumoren der Meningen Choroidplexustumor Delta-Thrombozytengranula-Mangel Melanozytose, diffuse leptomeningeale Seltene Blutgerinnungsstörung durch erworbene Blutplättchenanomalie Alpha-Granula-Defekt der Thrombozyten Sichelzellkrankheit mit assoziierter weiterer Hämoglobin-Anomalie Gliom Oligodendrogliom Choroid-Plexuskarzinom Fibrosarkom Weichteilsarkom Hämophilie B, schwere Osteosarkom Pinealislogentumor Hämophilie B, mittelschwere Sichelzellkrankheit HbSbeta-Thal Scott-Syndrom Seltene thrombotische Störung durch Gerinnungsfaktoren-Defekt Langerhans-Zell-Histiozytose der Kindheit Sebastian-Syndrom Oligodendrogliom, anaplastisches Von-Willebrand-Syndrom, erworbenes Schwannom, vestibuläres Keimzelltumor Choroidplexuspapillom, atypisches Liposarkom, myxoides/rundzelliges Pineoblastom Hämophilie A, schwere Tumor, atypischer teratoider Hämophilie A Seltene thrombotische Störung durch konstitutionellen Gerinnungsfaktoren-Defekt Liposarkom, pleomorphes Hämophilie B, milde Perineuriom Ependymom, niedriggradiges Seltener Tumor des Nervensystems Afibrinogenämie, familiäre Liposarkom, hochdifferenziertes Primäres Melanom des Zentralnervensystems Hämophilie A, mittelschwere Kaposi-Sarkom Hämophilie B Liposarkom, dedifferenziertes Pineozytom Seltene thrombotische Störung durch erworbenen Gerinnungsfaktoren-Defekt Rundzelltumor, desmoplastischer Dysfibrinogenämie, familiäre Neurofibrom Sichelzellkrankheit HbSC Hämorrhagische Krankheit durch Alpha-1-Antitrypsin Pittsburgh-Mutation Melanozytom, meningeales Myxofibrosarkom Hämangioblastom Synovialsarkom Bernard-Soulier-Syndrom Immunthrombozytopenie Sichelzellkrankheit HbSD Tumor, papillärer, der Pinealisregion Hämorrhagische Diathese durch Glykoprotein VI-Mangel Hämorrhagische Diathese durch Integrin alpha2-beta1-Mangel Seltene Blutgerinnungsstörung durch konstitutionellen Gerinnungsfaktoren-Defekt Seltene thrombotische Störung durch Blutplättchenanomalie Hämophilie A, milde Sichelzellkrankheit HbSE Tumoren der kranialen und spinalen Nerven Thrombozytopenie, autoimmune Testikulärer Keimzelltumor, nicht-seminomatöser Ependymom, anaplastisches Thrombopathie, konstitutionelle Pinealisparenchymtumor intermediärer Differenzierung Chondrosarkom, extraskelettales myxoides Hereditäre Persistenz des fetalen Hämoglobins mit Sichelzellkrankheit Tumor, neuronaler Tumor, oligoastrozytischer Schwannom, malignes Neurozytom, zentrales Oligoastrozytom Multiple Sklerose-Ichthyose-Faktor-VIII-Mangel-Syndrom Dermatofibrosarcoma protuberans Syndrome mit Alpha-Thalassämie als Hauptmerkmal Neurozytom, extraventrikuläres Vitamin K-abhängige Gerinnungsfaktoren, kongenitaler Mangel Gerinnungsstörung vom Ost-Texanischen Typ Tumor, gemischter neuro-glialer Pseudo-von-Willebrand-Syndrom Meningeom, multiples, familiäre Form Thrombotisch-thrombozytopenische Purpura, kongenitale Form Liponeurozytom, zerebelläres