Disease
Hematology
- Pyruvate Kinase Deficiency
- abilirubinuria jaundice syndrome
- acute hemorrhagic anemia
- Zygomycosis
- Paget's disease-like reticulocytosis
- erythropoietic porphyria
- eosinophilia
- eosinophilic leukemia
- Haemophilus influenzae skin infection
- post-transfusion thrombocytopenic purpura
- pine caterpillar osteoarthritis
- Leukopenia and agranulocytosis
- leukemia
- leukemic angina
- bleeding disorders
- pure red cell aplastic anemia
- Hypocalcemia and hypomagnesemia
- Thalassemia
- multiple myeloma
- malignant histiocytosis
- malignant lymphoma
- Bone marrow tuberculosis anemia
- myelofibrosis
- myelodysplastic syndrome
- Allergic purpura
- Acquired platelet dysfunction
- Acquired Circulatory Anticoagulant Hypertension Syndrome
- Hodgkin lymphoma
- macroglobulinemia
- acute leukemia
- megaloblastic anemia
- acute lymphoblastic leukemia
- lymphopenia
- sickle cell disease
- leukemia reaction
- agranulocytosis
- green tumor
- anemia of chronic disease
- disseminated intravascular coagulation
- chronic myelogenous leukemia
- chronic lymphocytic leukemia
- Congestive splenomegaly
- anemia
- Hypersplenism
- Glucose-6-phosphate dehydrogenase deficiency
- iron deficiency anemia
- Anemia due to excessive hemolysis
- hemolytic anemia
- eosinophilia
- idiopathic hypereosinophilic syndrome
- idiopathic thrombocytopenic purpura
- iron utilization anemia
- vitamin K deficiency
- thrombotic thrombocytopenic purpura
- Thrombocytopenia
- hemophilia
- congenital erythrocytic disease
- von Willebrand disease
- hereditary hemochromatosis
- Anemia due to folic acid deficiency
- hereditary hemorrhagic telangiectasia
- nutritional megaloblastic anemia
- idiopathic thrombocytopenic purpura
- essential thrombocythemia
- abnormal hemoglobinopathies
- neutropenia
- aplastic anemia
- autoimmune hemolytic anemia
- polycythemia vera
- paroxysmal nocturnal hemoglobinuria
- Anemia due to acute blood loss
- disseminated intravascular coagulation
- congenital pure red cell aplastic anemia
- congenital dyserythropoietic anemia
- myelo-pancreatic syndrome
- Alloimmune neonatal thrombocytopenic purpura
- Mycobacterium intracellularis infection
- Infectious lymphocytosis
- Geomycosis
- giant platelet disease
- arteriosclerosis obliterans
- giant cell arteritis 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 circulating anticoagulant hyperplasia
- Gitlin syndrome
- acute agranulocytosis
- acute lymphoblastic leukemia
- plasma cell leukemia
- Mycobacterium kansasii infection
- Mycobacterium ulcerans infection
- sickle cell anemia
- Blastomyces dermatitidis
- Light chain disease and light chain deposition disease
- Penicillosis
- Hemolytic anemia caused by arsine
- congenital leukemia
- relative polycythemia
- hereditary hemorrhagic telangiectasia
- Transient hypogammaglobulinemia in infancy
- neutropenia
- histiocytic necrotizing lymphadenitis
- Pseudomonas aeruginosa infection
- Infectious thrombocytopenic purpura
- Sulfhaemoglobinemia
- angioimmunoblastic lymphadenopathy
- thrombosis
- Alpha-reservoir disease
- Hodgkin's disease
- Nizhnov syndrome
- Anemia due to liver disease
- Pyrimidine 5'-nucleotide deficiency
- Allergic purpura nephritis
- acquired hemophilia
- Westcott-Aldrich syndrome
- hereditary protein C deficiency
- Serum sickness and serum sickness-like reactions
- primary cutaneous B-cell lymphoma
- Protoporphyria
- hypoproliferative acute leukemia
- toxic purpura
- Penicillosis marneffei
- Sepsis and Bacteremia
- Senile purpura
- congenital atransferrinemia
- Langerhans histiocytosis
- pure red blood cell aplasia
- Methotrexate-Associated Lymphoproliferative Disorders
- pediatric acute lymphoblastic leukemia
- congenital nonhemolytic jaundice
- hairy cell leukemia
- acute intermittent porphyria
- warm antibody autoimmune hemolytic anemia
- Hemolytic anemia caused by hyperthermia
- paroxysmal cold hemoglobinuria
- anemia of chronic disease
- geriatric acute leukemia
- purpura fulminans
- Hemolytic anemia due to lead poisoning
- secondary sideroblastic anemia
- lymphoma cell leukemia
- basophilic leukemia
- Mental disorders associated with leukemia
- Mental disorders associated with anemia
- hemolytic uremic syndrome
- Thrombocytopenia
- Hemophilia A
- folic acid deficiency
- chronic hematogenous osteomyelitis
- Anemia due to hypothyroidism
- chronic myeloid leukemia
- wound botulism
- leukemia kidney damage
- disseminated intravascular coagulation
- unstable hemoglobinopathies
- C5 insufficiency syndrome
- Castleman disease
- adult chronic myeloid leukemia
- Pasteurella haemorrhagic infection
- Skin manifestations of DF-2 sepsis
- delta-reservoir disease
- large granular lymphocytic leukemia
- monocytic leukemia
- reactive plasmacytosis
- acute nonlymphocytic leukemia in the elderly
- acute lymphoblastic leukemia in the elderly
- skin leukemia
- subcutaneous panniculitis inflammatory T-cell lymphoma
- amyloidosis
- Sinus histiocytosis with giant lymphadenopathy
- mast cell leukemia
- Pulmonary eosinophilic infiltrates
- Glucose phosphoisomerase deficiency
- bacillary epithelioid angiomatosis
- heparin-induced thrombocytopenia
- Anemia due to infectious disease
- high altitude polycythemia
- myelopathic anemia
- Mycobacterium chelae infection
- cavernous hemangioma thrombocytopenia syndrome
- erythropoietic protoporphyria
- anti-activated protein C disease
- necrotizing sarcoid-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 cutaneous follicular center cell lymphoma
- secondary thrombocytosis
- Acanthocytosis secondary to severe liver disease
- familial polycythemia
- capsular histoplasmosis
- progressive pigmented purpuric dermatosis
- stomatocytosis
- lazy leukocyte syndrome
- Histiocytosis of Langhans cells
- Leukopenia and agranulocytosis in the elderly
- sepsis in the elderly
- Disseminated intravascular coagulation in the elderly
- Hypocalcemia in the elderly
- Multiple Myeloma in the Elderly
- myelodysplastic syndrome in the elderly
- Allergic purpura in the elderly
- Hodgkin lymphoma in the elderly
- megaloblastic anemia in the elderly
- anemia of chronic disease 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
- Essential thrombocythemia in the elderly
- Aplastic anemia in the elderly
- polycythemia vera in the elderly
- cold antibody autoimmune hemolytic anemia
- cold agglutinin syndrome
- Cryoglobulinemia kidney damage
- Fusarium disease
- sickle cell nephropathy
- Mycobacterium scrofula infection
- chronic alcoholism
- chronic renal anemia
- Trichosporidiosis
- mucormycosis
- Rh incompatibility hemolytic disease
- telangiectatic annular purpura
- Melanie's Gangrene
- Meningococcal bacteremia
- skin lymphogranulomatosis
- Granulomatous loose skin
- Sezeri syndrome
- Sarcoidosis of the nervous system
- basophilia
- pediatric leukemia
- Acquired coagulation factor abnormalities due to severe liver disease
- myelomonocytic leukemia
- myeloperoxidase deficiency
- idiopathic delayed immunoglobulin deficiency
- idiopathic eosinophilic syndrome
- Hemolytic anemia due to copper poisoning
- Painful cyanosis syndrome
- microangiopathic hemolytic anemia
- centipede sting
- congenital agamma-globulinemia
- congenital aplastic anemia
- microscopic polyangiitis
- Pediatric alpha-thalassemia
- Pediatric beta thalassemia
- Pediatric Echo and Coxsackie Virus Infection
- pediatric adult chronic myeloid leukemia
- neonatal hemorrhage
- neonatal purpura
- marching hemoglobinuria
- Hemoglobin C disease
- Hemoglobin D disease
- Hemoglobin E disease
- Hemoglobin M disease
- Abnormal platelet procoagulant activity
- thrombocytopenic purpura
- platelet-type pseudovonoid hemophilia
- Hemophilia B
- Mycosis fungoides and Sezary syndrome
- drug immune thrombocytopenic purpura
- drug-related immune hemolytic anemia
- post-transplant lymphoproliferative disease
- Inherited protein S deficiency
- hereditary coproporphyria
- hereditary methemoglobinemia
- hereditary antithrombin III deficiency
- hereditary prothrombin deficiency
- Hereditary factor V deficiency
- Hereditary factor VII deficiency
- Hereditary factor XIII deficiency
- Hereditary factor X deficiency
- Hereditary factor XI deficiency
- hereditary spherocytosis
- hereditary sideroblastic anemia
- Hereditary Elliptocytosis
- hereditary fibrinogen deficiency
- hereditary dysfibrinogenemia
- abnormal gamma-globulinemia
- prolymphocytic leukemia
- juvenile myelomonocytic leukemia
- juvenile chronic myeloid leukemia
- Stasis purpura
- Lymphoproliferative disorders associated with primary immune disorders
- primary monoclonal immunoglobulin disease
- Primary hyperlipoproteinemia and xanthoma hyperplasia
- primary myelofibrosis
- Primary mixed cryoglobulinemic vasculitis
- primary macroglobulinemia
- primary macroglobulinemia renal impairment
- primary cutaneous immunocytoma
- primary fibrinolysis
- Toxic methemoglobinemia
- central nervous system leukemia
- neutropenia
- heavy chain disease
- thalassemia
- autoerythrocyte hypersensitivity purpura
- Broad bean disease
- chronic myelomonocytic leukemia
- blood poison
- blood stasis constitution
- congenital leukocyte dysgranulosis syndrome
- old rotten legs
- hypocalcemia
- Leukopenia
- nutritional anemia
- blood disease
- Congenital factor X deficiency
- hemolytic jaundice
- thick blood
- Microcytic hypochromic anemia
- acute myeloid leukemia