Disease
Hematology
- Pyruvate kinase deficiency
- Bilirubinuria jaundice syndrome
- Acute hemorrhagic anemia
- Zygomycosis
- Paget's disease like reticulosis
- Erythropoietic porphyria
- Eosinophilia
- Eosinophilic leukemia
- Skin infection by Haemophilus influenzae
- Post transfusion thrombocytopenic purpura
- Dendrolimus osteoarthritis
- Leukopenia and agranulocytosis
- leukemia
- Leukemic angina
- Hemorrhagic disease
- pure red cell aplasia
- Hypocalcemia and hypomagnesemia
- Thalassemia
- Multiple myeloma
- Malignant histiocytosis
- malignant lymphoma
- Tuberculous anemia of bone marrow
- Myelofibrosis
- Myelodysplastic syndrome
- allergic purpura
- Acquired platelet dysfunction
- Acquired circulating anticoagulant substance increase syndrome
- Hodgkin's lymphoma
- Megaglobulinemia
- acute leukemia
- Megaloblastic anemia
- Acute lymphocytic leukemia
- Lymphopenia
- Sickle cell disease
- Leukemoid reaction
- Agranulocytosis
- Chloroma
- Anemia of chronic disease
- Disseminated intravascular coagulation
- Chronic myeloid leukemia
- Chronic lymphocytic leukemia
- Congestive splenomegaly
- anemia
- Hypersplenism
- Glucose-6-phosphate dehydrogenase deficiency
- iron-deficiency anemia
- Anemia caused by hemolysis
- Hemolytic anemia
- Eosinophilia
- Idiopathic hypereosinophilic syndrome
- Idiopathic thrombocytopenic purpura
- Iron utilization anemia
- Vitamin K deficiency disease
- Thrombotic thrombocytopenic purpura
- Thrombocytopenia
- hemophilia
- Congenital erythrocyte membrane disease
- Von Willebrand disease
- Hereditary hemochromatosis
- Anemia due to folic acid deficiency
- Hereditary hemorrhagic telangiectasia
- Nutritional megaloblastic anemia
- Primary thrombocytopenic purple scar
- Primary thrombocytosis
- Abnormal hemoglobinopathy
- Neutropenia
- Aplastic anemia
- Autoimmune hemolytic anemia
- Polycythemia vera
- Paroxysmal nocturnal hemoglobinuria
- Anemia due to acute blood loss
- Diffuse intravascular coagulation
- Congenital pure red cell aplastic anemia
- Congenital erythropoietic anemia
- Bone marrow pancreatic syndrome
- Alloimmune neonatal thrombocytopenic purpura
- mycobacterium intracellulare infection
- Infectious lymphocytosis
- Geomycosis
- Giant thrombocytopathy
- Occlusive arteriosclerosis
- Giant cell arteritic scleritis
- Acute myeloid leukemia
- Chronic lymphocytic leukemia
- Leukocyte glucose-6-phosphate dehydrogenase deficiency
- Traumatic cardiogenic hemolytic anemia
- Adult T-cell leukemia
- Hyperimmunoglobulin E syndrome
- secondary leukemia
- Reactive histiocytosis
- Rheumatic anemia
- Acquired circulatory hypercoagulant syndrome
- Gitlin syndrome
- Acute agranulocytosis
- acute lymphoblastic leukemia
- Plasma cell leukemia
- mycobacterium kansasii infection
- mycobacterium ulcerans infection
- Sickle cell anemia
- Blastomyces dermatitis
- Light chain disease and light chain deposition disease
- Penicilliosis
- Hemolytic anemia caused by hydrogen arsenide
- Congenital leukemia
- Relative polycythemia
- Hereditary hemorrhagic telangiectasia
- Transient hypogammaglobulinemia in infancy
- Neutropenia
- Histiocytic necrotizing lymphadenitis
- Pseudomonas aeruginosa infection
- Infectious thrombocytopenic purpura
- Hemoglobinemia Sulfide
- Angioimmunoblastic lymphadenopathy
- Thrombosis
- α- Storage pool disease
- Hodgkin's disease
- Niznov syndrome
- Anemia due to liver disease
- Pyrimidine 5 ′ - nucleotide deficiency
- Henoch Schonlein purpura nephritis
- acquired hemophilia
- Viscott Aldrich syndrome
- Hereditary protein C deficiency
- Seropathy and serum disease like reaction
- Primary cutaneous B-cell lymphoma
- Protoporphyria
- Hypoproliferative acute leukemia
- Toxic purpura
- Penicillium marneffei
- sepsis and bacteremia
- Senile purpura
- Congenital nontransferrinemia
- Langerhans histiocytosis
- Pure red blood cell regeneration disorder
- Methotrexate related lymphoproliferative diseases
- Acute lymphocytic leukemia in children
- Congenital non hemolytic jaundice
- Hair cell leukemia
- Acute intermittent porphyria
- warm autoimmune hemolytic anemia
- Hemolytic anemia caused by high temperature
- Paroxysmal cold hemoglobinuria
- Chronic disease anemia
- Senile acute leukemia
- Fulminant purpura
- Hemolytic anemia caused by lead poisoning
- Secondary sideroblastic anemia
- Lymphoma cell leukemia
- Basophilic leukemia
- Mental disorders associated with leukemia
- Mental disorders associated with anemia
- Hemolytic uremic syndrome
- Thromboasthenia
- Hemophilia A
- Folate deficiency
- Chronic hematogenous osteomyelitis
- Anemia due to hypothyroidism
- Chronic myeloid leukemia
- Wound botulism
- Leukemic kidney damage
- Disseminated intravascular coagulation
- unstable hemoglobin disease
- C5 Dysfunction Syndrome
- Castleman disease
- Adult chronic myeloid leukemia
- Pasteurella haemorrhagica infection
- DF-2 Skin manifestations of septicemia
- δ- Storage pool disease
- Large granular lymphocytic leukemia
- Monocytic leukemia
- Reactive plasmacytosis
- Acute non lymphocytic leukemia in the elderly
- Acute lymphoblastic leukemia in the elderly
- Cutaneous leukemia
- Subcutaneous panniculitic T-cell lymphoma
- Amyloidosis
- Sinus histiocytosis with giant lymphadenopathy
- Mast cell leukemia
- Pulmonary eosinophil infiltration
- Glucose phosphate isomerase deficiency
- bacillary Epithelioid Angiomatosis
- Heparin induced thrombocytopenia
- Anemia due to infectious diseases
- High altitude polycythemia
- Myelopathic anemia
- mycodacterium chelonei infection
- Thrombocytopenia syndrome in cavernous hemangioma
- Erythropoietic protoporphyria
- Anti activated protein C syndrome
- Necrosarcoidoid granulomatosis
- Mixed porphyria
- Abnormality of acquired vitamin K dependent coagulation factor
- Acute eosinophilic pneumonia
- Acute myeloid leukemia
- Acute heterozygous leukemia
- Acute promyelocytic leukemia
- Hexokinase deficiency
- Secondary monoclonal immunoglobulin disease
- Secondary myelofibrosis
- Secondary polycythemia
- Secondary follicular central cell lymphoma of skin
- Secondary thrombocytosis
- Echinocytosis secondary to severe liver disease
- Familial polycythemia
- Histoplasmosis capsulatum
- Progressive pigmented purpura dermatosis
- Mouth polycythemia
- Lazy Leukocyte Syndrome
- Histiocytosis of Langhans cells
- Leukopenia and agranulocytosis in the elderly
- senile septicaemia
- Disseminated intravascular coagulation in the elderly
- Senile hypocalcemia
- Multiple myeloma in the elderly
- Myelodysplastic syndrome in the elderly
- Allergic purpura in the elderly
- Hodgkin's lymphoma in the elderly
- Megaloblastic anemia in the elderly
- Chronic disease anemia in the elderly
- Chronic myeloid leukemia in the elderly
- Chronic lymphocytic leukemia in the elderly
- Immune thrombocytopenic purpura in the elderly
- Iron deficiency anemia in the elderly
- Hemolytic anemia in the elderly
- Thrombotic disease in the elderly
- Primary myelofibrosis in the elderly
- Primary thrombocytosis in the elderly
- Aplastic anemia in the elderly
- Elderly polycythemia vera
- Cold resistant autoimmune hemolytic anemia
- Cold agglutinin syndrome
- Renal damage due to cryoglobulinemia
- Fusarium disease
- sickle cell nephropathy
- mycobacterium scrofulaceum infection
- Chronic alcoholism
- Chronic renal anemia
- Trichosporosis
- Mucormycosis
- Rh blood group incompatibility hemolysis
- Telangiectatic purpura annulata
- Melanie gangrene
- Meningococcemia
- Cutaneous lymphogranulomatosis
- Granulomatous flabby skin
- Szary syndrome
- Sarcoidosis of nervous system
- Basophilia
- Childhood leukemia
- Abnormal acquired coagulation factors caused by severe liver disease
- Myelomonocytic leukemia
- Myeloperoxidase deficiency
- Idiopathic delayed immunoglobulin deficiency
- Idiopathic eosinophilia syndrome
- Hemolytic anemia caused by copper poisoning
- Painful bruising syndrome
- Microvascular hemolytic anemia
- centipede sting
- Congenital synchondrosis γ- Globulinemia
- Congenital aplastic anemia
- microscopic polyangiitisMPA
- children α- Thalassemia
- children β Thalassemia
- Eckel and coxsackie virus infection in children
- Adult chronic myeloid leukemia in children
- Neonatal hemorrhage
- Purpura neonatorum
- Marching hemoglobinuria
- Hemoglobin C disease
- Hemoglobin D disease
- Hemoglobin E disease
- Hemoglobin M disease
- Abnormal platelet procoagulant activity
- Thrombocytopenic purpura
- Platelet pseudovascular hemophilia
- Hemophilia B
- Fungoid mycosis and Sezary syndrome
- drugs induced immune thrombocytopenic purpura
- Drug-related immune hemolytic anemia
- Post transplant lymphoproliferative disease
- Hereditary protein S deficiency
- Hereditary coprophyria
- Hereditary methemoglobinemia
- Hereditary antithrombin III deficiency
- Hereditary prothrombin deficiency
- Hereditary coagulation factor V deficiency
- Hereditary coagulation factor Ⅶ deficiency
- Hereditary coagulation factor XIII deficiency
- Hereditary coagulation factor X deficiency
- Hereditary coagulation factor XI deficiency
- Hereditary spherocytosis
- Hereditary sideroblastic anemia
- Hereditary elliptical polycythemia
- Hereditary fibrinogen deficiency
- Hereditary abnormal fibrinogenemia
- abnormal γ- Globulinemia
- Lymphoblastic leukemia
- Juvenile myelomonocytic leukemia
- Juvenile chronic myeloid leukemia
- Stasis purpura
- Lymphproliferative diseases associated with primary immune diseases
- Primary monoclonal immunoglobulin disease
- Primary hyperlipoproteinemia and xanthomatosis
- Primary myelofibrosis
- Primary mixed cryoglobulinemic vasculitis
- Primary macroglobulinemia
- Renal damage in primary megaglobulinemia
- Primary cutaneous immunocytoma
- Primary fibrinolysis
- Toxic methemoglobinemia
- Central nervous system leukemia
- Neutrophilia
- Heavy chain disease
- Thalassemia
- Autoerythrocytic anaphylactoid purpura
- Broad bean disease
- Chronic myelomonocytic leukemia
- Blood poison
- Blood stasis constitution
- Congenital Leukocyte Granular Abnormality Syndrome
- Old rotten leg
- Hypocalcemia
- Leukopenia
- Nutritional anemia
- Hematopathy
- Congenital factor X deficiency
- Hemolytic jaundice
- Blood thickened
- Microcytic hypochromic anemia
- Acute myeloid leukemia