Disease
Hematology
- Pyruvate kinase deficiency
- No biliary pigmentary urinary jaundice syndrome
- Acute hemorrhagic anemia
- Zygomycosis
- Paget's disease-like reticulosis
- Erythropoietic porphyria
- Eosinophilia
- Eosinophilic leukemia
- Skin infection of Haemophilus influenzae
- Thrombocytopenic purpura after transfusion
- Pine caterpillar osteoarthritis
- Leukopenia and agranulocytosis
- leukemia
- Leukemia angina
- Hemorrhagic disease
- Simple red blood cell aplastic anemia
- Hypocalcemia and hypomagnesemia
- Thalassemia
- Multiple myeloma
- Malignant histiocytosis
- Malignant lymphoma
- Bone marrow anemia
- Myelofibrosis
- Myelodysplastic syndrome
- Allergic purpura
- Acquired platelet dysfunction
- Acquired circulatory anticoagulant syndrome
- Hodgkin's lymphoma
- Macroglobulinemia
- Acute leukemia
- Megaloblastic anemia
- Acute lymphocytic leukemia
- Lymphopenia
- Sickle cell disease
- Leukemia-like reaction
- Agranulocytosis
- Green tumor
- Anemia of chronic diseases
- Disseminated intravascular coagulation
- Chronic myeloid leukemia
- Chronic lymphocytic leukemia
- Congestive splenomegaly
- anemia
- Hypersplenism
- Glucose-6-phosphate dehydrogenase deficiency
- Iron deficiency anemia
- Anemia caused by excessive hemolysis
- Hemolytic anemia
- Eosinophilia
- Idiopathic hypereosinophilic syndrome
- Idiopathic thrombocytopenic purpura
- Iron utilization anemia
- Vitamin K deficiency
- Thrombotic thrombocytopenic purpura
- Thrombocytopenia
- hemophilia
- Congenital erythrocyte disease
- Vascular hemophilia
- Hereditary hemochromatosis
- Anemia caused by folic acid deficiency
- Hereditary hemorrhagic telangiectasia
- Nutritional giant erythrocyte anemia
- Primary thrombocytopenic purpura
- Essential thrombocytopenia
- Abnormal hemoglobinopathy
- Neutral white (granulocytopenia)
- Aplastic anemia
- Autoimmune hemolytic anemia
- Polycythemia vera
- Paroxysmal nocturnal hemoglobinuria
- Anemia caused by acute blood loss
- Diffuse intravascular coagulation
- Congenital pure red blood cell aplastic anemia
- Congenital erythropoiesis abnormal anemia
- Bone marrow-pancreatic syndrome
- Immune neonatal thrombocytopenic purpura
- Intracellular mycobacterial infection
- Infectious lymphocytosis
- Geotricemia
- Giant platelet disease
- Occlusive arteriosclerosis
- Giant cell arterial scleritis
- Acute myeloid leukemia
- Chronic lymphocyte leukemia
- Leukocyte glucose-6-phosphate dehydrogenase deficiency
- Traumatic cardiogenic hemolytic anemia
- Adult T cell leukemia
- High immunoglobulin E syndrome
- Secondary leukemia
- Reactive histiocytosis
- Rheumatic anemia
- Acquired circulating anticoagulant
- Gitlin syndrome
- Acute neutropenia
- Acute lymphoblastic leukemia
- Plasma cell leukemia
- Kansas Mycobacterium infection
- Mycobacterium tuberculosis infection
- Sickle cell anemia
- Dermatitis bud
- Light chain disease and light chain deposition disease
- Penicillium
- Hemolytic anemia caused by arsine
- Congenital leukemia
- Relative polycythemia
- Hereditary hemorrhagic telangiectasia
- Transient hypogammaglobulinemia
- Neutropenia
- Tissue necrotic lymphadenitis
- Pseudomonas aeruginosa infection
- Infectious thrombocytopenic purpura
- Sulfated hemoglobinemia
- Angioimmunoblastic lymphadenopathy
- Thrombosis
- Alpha-storage disease
- Hodgkin's disease
- Niznov syndrome
- Anemia caused by liver disease
- Pyrimidine 5'-nucleotide deficiency
- Allergic purpura nephritis
- Acquired hemophilia
- Wiscott-Aldrich syndrome
- Hereditary protein C deficiency
- Serum and serum-like reactions
- Primary cutaneous B-cell lymphoma
- Protoporphyrin
- Hypoplastic acute leukemia
- Toxic purpura
- Marniffe blue mold
- Sepsis and bacteremia
- Senile sable
- Congenital no transferrinemia
- Langerhans histiocytosis
- Pure red cell aplasia
- Methotrexate-associated lymphoproliferative disorders
- Pediatric acute lymphocytic leukemia
- Congenital non-hemolytic jaundice
- Hairy cell leukemia
- Acute intermittent porphyria
- Thermo-antibody autoimmune hemolytic anemia
- Hemolytic anemia caused by high temperature
- Paroxysmal cold hemoglobinuria
- Chronic anemia
- Senile acute leukemia
- Fulminating purpura
- Hemolytic anemia caused by lead poisoning
- Secondary iron granulocyte anemia
- Lymphoma cell leukemia
- Basophilic leukemia
- Leukemia associated with mental disorders
- Mental disorder associated with anemia
- Hemolytic uremic syndrome
- Platelet weakness
- Hemophilia A
- Folic acid deficiency
- Chronic blood-borne osteomyelitis
- Anemia caused by hypothyroidism
- Chronic myeloid leukemia
- Burn botulism
- Leukemia and kidney damage
- Disseminated intravascular coagulation
- Unstable hemoglobinopathy
- C5 dysfunction syndrome
- Castleman disease
- Adult chronic myeloid leukemia
- Hemorrhagic Pasteurella infection
- Skin manifestations of DF-2 sepsis
- -storage disease
- Large granular lymphocyte leukemia
- Monocytic leukemia
- Reactive plasmacytosis
- Elderly acute non-lymphocytic leukemia
- Elderly acute lymphoblastic leukemia
- Skin leukemia
- Subcutaneous panniculitis T-cell lymphoma
- Amyloidosis
- Sinus histiocytosis with giant lymphadenopathy
- Mast cell leukemia
- Pulmonary eosinophilic infiltration
- Glucose phosphate isomerase deficiency
- Bacillus epithelioid angiomatosis
- Heparin-induced thrombocytopenia
- Anemia caused by infectious diseases
- Plateau polycythemia
- Bone marrow anemia
- Mycobacterium tuberculosis infection
- Cavernous hemangioma thrombocytopenia syndrome
- Erythropoiesis protoporphyrin
- Anti-activated protein C
- Necrotizing sarcoidosis-like granulomatosis
- Mixed porphyria
- Acquired vitamin K-dependent coagulation factor abnormalities
- Acute eosinophilic pneumonia
- Acute myeloid leukemia
- Acute heterozygous leukemia
- Acute promyelocytic leukemia
- Hexokinase deficiency
- Secondary monoclonal immunoglobulin disease
- Secondary myelofibrosis
- Secondary polycythemia
- Secondary skin follicular central cell lymphoma
- Secondary thrombocytosis
- Erythrocytosis secondary to severe liver disease
- Familial polycythemia
- Capsular histoplasmosis
- Progressive pigmentary purpuric dermatophytosis
- Oral polycythemia
- Lazy white blood cell syndrome
- Histiocytosis of Langhans cells
- Elderly leukopenia and agranulocytosis
- Septicemia in the elderly
- Disseminated intravascular coagulation in the elderly
- Elderly hypocalcemia
- Multiple myeloma in the elderly
- Elderly myelodysplastic syndrome
- Allergic purpura in the elderly
- Hodgkin's lymphoma
- Giant megaloblastic anemia in the elderly
- Chronic disease anemia in the elderly
- Chronic myeloid leukemia in the elderly
- Elderly chronic lymphocytic leukemia
- Elderly immune thrombocytopenic purpura
- Iron deficiency anemia in the elderly
- Hemolytic anemia in the elderly
- Elderly thrombotic disease
- Primary myelofibrosis in the elderly
- Elderly patients with essential thrombocytopenia
- Aplastic anemia in the elderly
- Elderly polycythemia
- Cold antibody type autoimmune hemolytic anemia
- Cold agglutinin syndrome
- Cryoglobulinemia kidney damage
- Fusarium disease
- Sickle cell nephropathy
- Mycobacterium infection
- Chronic alcoholism
- Chronic renal anemia
- Trichosporosis
- Mucor
- Rh blood group is not hemolytic disease
- Capillary dilatation
- Melanie gangrene
- Meningococcalemia
- Pediatric lymphogranuloma
- Granulomatous loose skin
- Sezeri syndrome
- Nervous system sarcoidosis
- Basophilic
- Pediatric leukemia
- Severe liver disease causes acquired clotting factor abnormalities
- Medullary monocytic leukemia
- Myeloperoxidase deficiency
- Idiopathic delayed immunoglobulin deficiency
- Idiopathic eosinophilia syndrome
- Hemolytic anemia caused by copper poisoning
- Painful bruising syndrome
- Microangiopathic hemolytic anemia
- centipede sting
- Congenital gamma-globulinemia
- Congenital aplastic anemia
- Miniature polyangiitis
- Pediatric alpha-thalassemia
- Pediatric beta thalassemia
- Pediatric and Coxsackie virus infection
- Adult adult chronic myeloid leukemia
- Neonatal hemorrhagic disease
- Neonatal purpura
- Marching hemoglobinuria
- Hemoglobin C disease
- Hemoglobin D disease
- Hemoglobin E disease
- Hemoglobin M disease
- Abnormal platelet procoagulant activity
- Thrombocytopenic purpura
- Platelet-type pseudovascular hemophilia
- Hemophilia B
- Mycosis fungoides and Sezary syndrome
- Drug-induced thrombocytopenic purpura
- Drug-related immune hemolytic anemia
- Post-transplant lymphoproliferative disease
- Hereditary protein S deficiency
- Hereditary fecal porphyria
- Hereditary methemoglobinemia
- Hereditary antithrombin III deficiency
- Hereditary prothrombin deficiency
- Hereditary coagulation factor V deficiency
- Hereditary factor VII deficiency
- Hereditary coagulation factor XIII deficiency
- Hereditary coagulation factor X deficiency
- Hereditary factor XI deficiency
- Hereditary spherocytosis
- Hereditary iron granulocyte anemia
- Hereditary elliptic polycythemia
- Hereditary fibrinogen deficiency
- Hereditary abnormal fibrinogenemia
- Abnormal gamma globulinemia
- Young lymphocytic leukemia
- Juvenile granulocyte-monocytic leukemia
- Juvenile chronic myeloid leukemia
- Stasis purpura
- Primary proliferative disease-associated lymphoproliferative disease
- Primary monoclonal immunoglobulin disease
- Primary hyperlipoproteinemia and xanthoma
- Primary myelofibrosis
- Primary mixed cryoglobulinemia vasculitis
- Primary macroglobulinemia
- Primary macroglobulinemia kidney damage
- Primary cutaneous immune cell tumor
- Primary fibrinolysis
- Toxic methemoglobinemia
- Central nervous system leukemia
- Neutrophilemia
- Heavy chain disease
- Ovoglobin-producing anemia
- Autologous red blood cell allergic purpura
- Broad bean disease
- Chronic myelomonocytic leukemia
- Blood poison
- Bloody constitution
- Congenital leukocyte abnormality syndrome
- Old rotten leg
- Hypocalcemia
- Leukopenia
- Nutritional anemia
- Blood disease
- Congenital X factor deficiency
- Hemolytic jaundice
- Blood thick
- Small cell hypochromic anemia
- Acute granulocytic leukemia