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About:
http://dbpedia.org/class/yago/BloodDyscrasia114053850
An Entity of Type:
Thing
,
from Named Graph:
http://dbpedia.org
,
within Data Space:
dbpedia.org
Property
Value
rdfs:
subClassOf
yago
:Dyscrasia114053717
owl:
equivalentClass
yago-res
:wordnet_blood_dyscrasia_114053850
is
rdf:
type
of
dbr
:B-cell_chronic_lymphocytic_leukemia
dbr
:Pure_red_cell_aplasia
dbr
:Muckle–Wells_syndrome
dbr
:Monoclonal_gammopathy_of_undetermined_significance
dbr
:Blood_stasis
dbr
:Hodgkin's_lymphoma
dbr
:Homocystinuria
dbr
:Hypereosinophilic_syndrome
dbr
:Hyperimmunoglobulin_E_syndrome
dbr
:Beta_thalassemia
dbr
:Peginesatide
dbr
:Pelger–Huet_anomaly
dbr
:Cutaneous_lymphoid_hyperplasia
dbr
:Von_Willebrand_disease
dbr
:Ineffective_erythropoiesis
dbr
:Leukostasis
dbr
:Light_chain_deposition_disease
dbr
:Vitamin_B12_deficiency
dbr
:Nutritional_anemia
dbr
:Pseudothrombocytopenia
dbr
:Common_variable_immunodeficiency
dbr
:Mastocytosis
dbr
:Myeloproliferative_neoplasm
dbr
:Pyknocytosis
dbr
:Chronic_myelogenous_leukemia
dbr
:Gaucher's_disease
dbr
:Glanzmann's_thrombasthenia
dbr
:Graft-versus-host_disease
dbr
:Mycosis_fungoides
dbr
:Myelodysplastic_syndrome
dbr
:Congenital_dyserythropoietic_anemia
dbr
:Congenital_dyserythropoietic_anemia_type_I
dbr
:Congenital_dyserythropoietic_anemia_type_II
dbr
:Congenital_dyserythropoietic_anemia_type_III
dbr
:Congenital_dyserythropoietic_anemia_type_IV
dbr
:Congenital_hemolytic_anemia
dbr
:Congenital_hypoplastic_anemia
dbr
:Cryoglobulinemia
dbr
:Erdheim–Chester_disease
dbr
:Ornithinaemia
dbr
:Anemia
dbr
:Anti-thymocyte_globulin
dbr
:Antiphospholipid_syndrome
dbr
:Bernard–Soulier_syndrome
dbr
:Leukemoid_reaction
dbr
:MALT_lymphoma
dbr
:Malignant_histiocytosis
dbr
:Cholemia
dbr
:Haemophilia_A
dbr
:Haemophilia_B
dbr
:Hematidrosis
dbr
:Hematologic_disease
dbr
:Hemolysis_(microbiology)
dbr
:Hemolytic_disease_of_the_newborn
dbr
:Idiopathic_CD4+_lymphocytopenia
dbr
:POEMS_syndrome
dbr
:Paroxysmal_cold_hemoglobinuria
dbr
:Paroxysmal_nocturnal_hemoglobinuria
dbr
:Plummer–Vinson_syndrome
dbr
:Post-transfusion_purpura
dbr
:Protein_S_deficiency
dbr
:Macroglobulinemia
dbr
:Tumor_lysis_syndrome
dbr
:May–Hegglin_anomaly
dbr
:McFall_v._Shimp
dbr
:Spherocytosis
dbr
:Venom-induced_consumption_coagulopathy
dbr
:Burkitt's_lymphoma
dbr
:Activated_protein_C_resistance
dbr
:Acute_posthemorrhagic_anemia
dbr
:Thrombotic_thrombocytopenic_purpura
dbr
:Waldenström's_macroglobulinemia
dbr
:Wiskott–Aldrich_syndrome
dbr
:HELLP_syndrome
dbr
:Iron-deficiency_anemia
dbr
:Iron_deficiency
dbr
:Essential_thrombocytosis
dbr
:Lines_of_Zahn
dbr
:Kostmann_syndrome
dbr
:Acute_erythroid_leukemia
dbr
:Acute_promyelocytic_leukemia
dbr
:Alpha-thalassemia
dbr
:Anaplastic_large-cell_lymphoma
dbr
:Cutaneous_T_cell_lymphoma
dbr
:Fanconi_anemia
dbr
:Follicular_lymphoma
dbr
:Anemia_of_chronic_disease
dbr
:Anemia_of_prematurity
dbr
:Non-Hodgkin_lymphoma
dbr
:Diamond–Blackfan_anemia
dbr
:Folate_deficiency
dbr
:Glucose-6-phosphate_dehydrogenase_deficiency
dbr
:Gray_platelet_syndrome
dbr
:Delta-thalassemia
dbr
:Left_shift_(medicine)
dbr
:Hairy_cell_leukemia
dbr
:Hemolytic-uremic_syndrome
dbr
:Hemophagocytic_lymphohistiocytosis
dbr
:Henoch–Schönlein_purpura
dbr
:Hereditary_elliptocytosis
dbr
:Hereditary_stomatocytosis
dbr
:Atypical_hemolytic_uremic_syndrome
dbr
:Bahima_disease
dbr
:Hyperviscosity_syndrome
dbr
:Hypouricemia
dbr
:Rh_disease
dbr
:Juvenile_myelomonocytic_leukemia
dbr
:Langerhans_cell_histiocytosis
dbr
:Bisalbuminemia
dbr
:Bleeding_diathesis
dbr
:Blood_hammer
dbr
:Sézary_disease
dbr
:Coagulopathy
dbr
:Cold_agglutinin_disease
dbr
:Heparin-induced_thrombocytopenia
dbr
:Hepatic_veno-occlusive_disease
dbr
:Hereditary_persistence_of_fetal_hemoglobin
dbr
:Hereditary_spherocytosis
dbr
:Hexokinase_deficiency
dbr
:Southeast_Asian_ovalocytosis
dbr
:DiGeorge_syndrome
dbr
:Disseminated_intravascular_coagulation
dbr
:Autoimmune_hemolytic_anemia
dbr
:Bone_marrow_failure
dbr
:Polycythemia_vera
dbr
:Fibrinogenolysis
dbr
:Internal_bleeding
dbr
:Methemoglobinemia
dbr
:Neonatal_alloimmune_thrombocytopenia
dbr
:X-linked_agammaglobulinemia
dbr
:McLeod_syndrome
dbr
:Microangiopathic_hemolytic_anemia
dbr
:Minimal_residual_disease
dbr
:Factor_V_Leiden
dbr
:Gunther_disease
dbr
:Imerslund–Gräsbeck_syndrome
dbr
:Triosephosphate_isomerase_deficiency
dbr
:Rosai–Dorfman_disease
dbr
:Evans_syndrome
dbr
:Management_of_thalassemia
dbr
:Protein_C_deficiency
dbr
:Myelophthisic_anemia
dbr
:Sickle_cell_trait
dbr
:Pyruvate_kinase_deficiency
dbr
:Non-sideropenic_hypochromic_anaemia
dbr
:Trauma_triad_of_death
dbr
:Thrombophilia
dbr
:Zieve's_syndrome
dbr
:Splenic_injury
dbr
:Shwachman–Diamond_syndrome
dbr
:No_reflow_phenomenon
dbr
:Normochromic_anemia
dbr
:Normocytic_anemia
dbr
:Juvenile_megaloblastic_anaemia_1
dbr
:Panmyelosis
dbr
:Thrombohemorrhagic_event
dbr
:Paraproteinemia
dbr
:Rh_deficiency_syndrome
dbr
:TAR_syndrome
is
rdfs:
subClassOf
of
yago
:BloodDisease114189204
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