WordNet an impairment of health or a condition of abnormal functioning
caused by or altered by or manifesting disease or pathology; "diseased tonsils"; "a morbid growth"; "pathologic tissue"; "pathological bodily processes" (同)morbid , pathologic , pathological
of or relating to or involved in hematology (同)haematological , hematological PrepTutorEJDIC (体の)『病気』,疾患 / (精神・道徳などの)病気,病弊
女性の話術芸人 =diseur
病気にかかった / 病的な,不健全な(morbid) Wikipedia preview 出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2019/04/16 07:31:21」(JST)
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Hematologic disease Specialty Hematology
Hematologic diseases are disorders which primarily affect the blood. Hematology includes the study of these disorders.
Myeloid Hemoglobinopathies (congenital abnormality of the hemoglobin molecule or of the rate of hemoglobin synthesis)
Sickle-cell disease
Thalassemia
Methemoglobinemia Anemias (lack of red blood cells or hemoglobin)
Iron deficiency anemia
Megaloblastic anemia
Vitamin B12 deficiency
Folate deficiency
Hemolytic anemias (destruction of red blood cells)
Genetic disorders of RBC membrane
Hereditary spherocytosis
Hereditary elliptocytosis
Congenital dyserythropoietic anemia
Genetic disorders of RBC metabolism
Glucose-6-phosphate dehydrogenase deficiency (G6PD)
Pyruvate kinase deficiency
Immune mediated hemolytic anemia (direct Coombs test is positive)
Autoimmune hemolytic anemia
Warm antibody autoimmune hemolytic anemia
Idiopathic
Systemic lupus erythematosus (SLE)
Evans' syndrome (antiplatelet antibodies and hemolytic antibodies)
Cold autoimmune hemolytic anemia
Cold agglutinin disease
Paroxysmal cold hemoglobinuria (rare)
Infectious mononucleosis
Alloimmune hemolytic anemia
Hemolytic disease of the newborn (HDN)
Rh disease (Rh D)
ABO hemolytic disease of the newborn
Anti-Kell hemolytic disease of the newborn
Rhesus c hemolytic disease of the newborn
Rhesus E hemolytic disease of the newborn
Other blood group incompatibility (RhC, Rhe, Kid, Duffy, MN, P and others)
Drug induced immune mediated hemolytic anemia
Penicillin (high dose)
Methyldopa
Hemoglobinopathies (where these is an unstable or crystalline hemoglobin)
Paroxysmal nocturnal hemoglobinuria (rare acquired clonal disorder of red blood cell surface proteins)
Direct physical damage to RBCs
Microangiopathic hemolytic anemia
Secondary to artificial heart valve(s)
Aplastic anemia
Fanconi anemia
Diamond-Blackfan anemia (inherited pure red cell aplasia)
Acquired pure red cell aplasia Decreased numbers of cells
Myelodysplastic syndrome
Myelofibrosis
Neutropenia (decrease in the number of neutrophils)
Agranulocytosis
Glanzmann's thrombasthenia
Thrombocytopenia (decrease in the number of platelets)
Idiopathic thrombocytopenic purpura (ITP)
Thrombotic thrombocytopenic purpura (TTP)
Heparin-induced thrombocytopenia (HIT) Myeloproliferative disorders (Increased numbers of cells)
Polycythemia vera (increase in the number of cells in general)
Erythrocytosis (increase in the number of red blood cells)
Leukocytosis (increase in the number of white blood cells)
Thrombocytosis (increase in the number of platelets)
Myeloproliferative disorder
Transient myeloproliferative disease Coagulopathies (disorders of bleeding and coagulation)
Thrombocytosis
Recurrent thrombosis
Disseminated intravascular coagulation
Disorders of clotting proteins
Hemophilia
Hemophilia A
Hemophilia B (also known as Christmas disease)
Hemophilia C
Von Willebrand disease
Disseminated intravascular coagulation
Protein S deficiency
Antiphospholipid syndrome
Disorders of platelets
Thrombocytopenia
Glanzmann's thrombasthenia
Wiskott-Aldrich syndrome Hematological malignancies Hematological malignancies
Lymphomas
Hodgkin's disease
Non-Hodgkin's lymphoma {includes the next five entries}
Burkitt's lymphoma
Anaplastic large cell lymphoma
Splenic marginal zone lymphoma
Hepatosplenic T-cell lymphoma
Angioimmunoblastic T-cell lymphoma (AILT)
Myelomas
Multiple myeloma
Waldenström macroglobulinemia
Plasmacytoma
Leukemias increased WBC
Acute lymphocytic leukemia (ALL)
Chronic lymphocytic leukemia (CLL){now included in theCLL/SCLL type NHL}
Acute myelogenous leukemia (AML)
Acute megakaryoblastic leukemia (AMKL), a sub-type of acute myelogenous leukemia
Chronic Idiopathic Myelofibrosis (MF)
Chronic myelogenous leukemia (CML)
T-cell prolymphocytic leukemia (T-PLL)
B-cell prolymphocytic leukemia (B-PLL)
Chronic neutrophilic leukemia (CNL)
Hairy cell leukemia (HCL)
T-cell large granular lymphocyte leukemia (T-LGL)
Aggressive NK-cell leukemia Miscellaneous Hemochromatosis
Asplenia
Hypersplenism
Monoclonal gammopathy of undetermined significance
Hemophagocytic lymphohistiocytosis
Tempi syndrome Hematological changes secondary to non-hematological disorders Anemia of chronic disease
Infectious mononucleosis
AIDS
Malaria
Leishmaniasis References
External links http://www.hematologic.niddk.nih.gov/info/index.htm
Diseases of red blood cells (D50–69,74, 280–287)
↑
↓
Anemia
Nutritional
Micro-: Iron-deficiency anemia
Macro-: Megaloblastic anemia
Hemolytic
Hereditary
enzymopathy: Glucose-6-phosphate dehydrogenase deficiencyglycolysis
pyruvate kinase deficiency
triosephosphate isomerase deficiency
hexokinase deficiency hemoglobinopathy: Thalassemia
Sickle-cell disease/trait
Hereditary persistence of fetal hemoglobin membrane: Hereditary spherocytosis
Minkowski–Chauffard syndrome Hereditary elliptocytosis
Southeast Asian ovalocytosis
Hereditary stomatocytosis Acquired
AIHA
Warm autoimmune hemolytic anemia
Cold agglutinin disease
Primary cold agglutinin disease
Secondary cold agglutinin syndrome
Donath–Landsteiner hemolytic anemia
Paroxysmal cold hemoglobinuria
Mixed autoimmune hemolytic anemia
membrane
paroxysmal nocturnal hemoglobinuria Microangiopathic hemolytic anemia
Thrombotic microangiopathy
Hemolytic-uremic syndrome Drug-induced autoimmune
Drug-induced nonautoimmune Hemolytic disease of the newborn
Aplastic
Hereditary: Fanconi anemia
Diamond–Blackfan anemia
Acquired: Pure red cell aplasia
Sideroblastic anemia
Myelophthisic Blood tests
Mean corpuscular volume
normocytic
microcytic
macrocytic Mean corpuscular hemoglobin concentration
Other
Methemoglobinemia
Sulfhemoglobinemia
Reticulocytopenia
Diseases of clotting (D50–69,74, 280–287)
Coagulation/
↑
Hyper-
primary: Antithrombin III deficiencyProtein C deficiency/Activated protein C resistance/Protein S deficiency/Factor V Leiden
Prothrombin G20210A
Sticky platelet syndrome acquired: Thrombocytosis
DIC
autoimmune
↓
Hypo-
Thrombocytopenia
Thrombocytopenic purpura: ITP
TM
TTP
Upshaw Schulman syndrome Heparin-induced thrombocytopenia
May–Hegglin anomaly Platelet function
adhesion
aggregation
Glanzmann's thrombasthenia platelet storage pool deficiency
Hermansky–Pudlak syndrome
Gray platelet syndrome Clotting factor
Hemophilia
von Willebrand disease
Hypoprothrombinemia/II
Factor VII deficiency
Factor X deficiency
Factor XII deficiency
Factor XIII deficiency
Dysfibrinogenemia
Congenital afibrinogenemia
Hematologic disease: Monocyte and granulocyte disease (CFU-GM/CFU-Baso/CFU-Eos), including immunodeficiency (D70-D71, 288)
Monocytes/
↑
Histiocytosis
Chronic granulomatous disease -cytosis:
↓
Granulocytes
↑
-cytosis:
granulocytosis
Neutrophilia
Eosinophilia/Hypereosinophilic syndrome
Basophilia
Bandemia
↓
-penia:
Granulocytopenia/agranulocytosis (Neutropenia/Kostmann syndrome
Eosinopenia
Basopenia)
PBD
chemotaxis/degranulation:
Leukocyte adhesion deficiency
Chédiak–Higashi syndrome
Neutrophil-specific granule deficiency respiratory burst:
Chronic granulomatous disease
Neutrophil immunodeficiency syndrome
Myeloperoxidase deficiency
Certain conditions originating in the perinatal period / fetal disease (P, 760–779)
Maternal factors and
placenta:
Placenta praevia
Placental insufficiency
Twin-to-twin transfusion syndrome chorion/amnion: umbilical cord:
Umbilical cord prolapse
Nuchal cord
Single umbilical artery
Length of gestation
Small for gestational age/Large for gestational age
Preterm birth/Postmature birth
Intrauterine growth restriction Birth trauma
scalp
Cephalhematoma
Chignon
Caput succedaneum
Subgaleal hemorrhage Brachial plexus lesion
Erb's palsy
Klumpke paralysis By system
Respiratory
Intrauterine hypoxia
Infant respiratory distress syndrome
Transient tachypnea of the newborn
Meconium aspiration syndrome
pleural disease
Pneumothorax
Pneumomediastinum Wilson–Mikity syndrome
Bronchopulmonary dysplasia Cardiovascular
Pneumopericardium
Persistent fetal circulation Haemorrhagic and
Vitamin K deficiency
Haemorrhagic disease of the newborn HDN
ABO
Anti-Kell
Rh c
Rh D
Rh E
Hydrops fetalis
Hyperbilirubinemia
Kernicterus
Neonatal jaundice Velamentous cord insertion
Intraventricular hemorrhage
Germinal matrix hemorrhage
Anemia of prematurity Digestive
Ileus
Necrotizing enterocolitis
Meconium peritonitis Integument and
Erythema toxicum
Sclerema neonatorum Nervous system
Perinatal asphyxia
Periventricular leukomalacia Musculoskeletal
Gray baby syndrome
muscle tone
Congenital hypertonia
Congenital hypotonia
Infectious
Vertically transmitted infection
Neonatal infection
Congenital rubella syndrome
Neonatal herpes simplex
Mycoplasma hominis infection
Ureaplasma urealyticum infection
Omphalitis
Neonatal sepsis
Group B streptococcal infection
Neonatal conjunctivitis Other
Miscarriage
Perinatal mortality
Stillbirth
Infant mortality
Neonatal withdrawal
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特定の原因、病態生理、症状、経過、予後、病理組織所見が全てそろった場合 (PSY.9) something that is very wrong with people's attitudes, way of life or with society. 関
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