Hematology
A
- AA (amyloidosis)
- AA (aplastic anemia)
- ACD
- Acquired thrombophilia
- Acute event-related anemia
- Acute GVHD
- Acute hemolytic reaction
- Acute lymphoblastic leukemia
- Acute myeloid leukemia
- Agnogenic myeloid metaplasia (AMM)
- AL
- AL amyloidosis
- Aldrich syndrome
- ALL
- Alpha-(alpha) thalassemia
- Alpha-thal
- Alpha-thalassemia
- Alpha-thalassemia major
- AML
- Amyloid
- Amyloidosis
- Anaphylactic transfusion reaction
- Anemia (evaluation of)
- Anemia of chronic disease
- Anemia of chronic inflammation
- Anemia of critical illness
- Anemia of inflammation
- Antiphospholipid antibodies
- Antiphospholipid antibody syndrome
- Antiphospholipid syndrome
- Aplastic anemia in adults
- APS
- Attenuated WAS (XLT)
- Atypical preeclampsia
B
- Babesia infection
- Babesiosis
- Beta-thalassemia
- Beta-thalassemia intermedia
- Beta-thalassemia major
- Beta-thalassemia minor
- Blast crisis
- Blast phase of chronic myelogenous leukemia
- Blastic CML
C
- Cbl deficiency
- Chlorosis
- Chronic GVHD
- Chronic lymphocytic leukemia
- Chronic myelogenous leukemia
- Chronic myeloid leukemia
- CLL
- CML
- Cobalamin deficiency
- Congenital bone marrow failure syndromes
- Congenital spherocytic hemolytic anemia
- Congenital spherocytosis
- Cooley anemia
D
E
- Easy bruising (evaluation of)
- Eczema-thrombocytopenia-immunodeficiency syndrome
- Eosinophilia (evaluation of)
- Essential thrombocythemia
- Essential thrombocytosis
- ET
- Evaluation of anemia
- Evaluation of easy bruising
- Evaluation of eosinophilia
- Evaluation of jaundice
- Evaluation of monoclonal gammopathies
- Evaluation of neutropenia
- Evaluation of neutrophilia
- Evaluation of pancytopenia
- Evaluation of splenomegaly
- Evaluation of thrombocytopenia
- Evaluation of unintentional weight loss
F
- Factor VIII deficiency
- Febrile neutropenia
- Febrile nonhemolytic transfusion reaction
- Felty syndrome
- Fever and neutropenia
- Folate deficiency
- Folic acid deficiency
- FS
G
- Gene map locus Xp11.23-p11.22
- Graft versus host disease
- Graft vs Host disease
- Graft-versus-Host
- Granulocytic sarcoma
- GVHD
H
- HA
- Hairy cell leukemia
- HCL
- HELLP syndrome
- Hemoglobin Bart hydrops fetalis syndrome (Hb Bart)
- Hemoglobin Constant Spring (Hb CS)
- Hemoglobin H (Hb H)
- Hemoglobin H hydrops fetalis syndrome
- Hemoglobin H/Constant Spring (Hb H/CS)
- Hemoglobin SC (HbSC) disease
- Hemoglobinopathy
- Hemolysis, elevated liver enzymes, low platelet syndrome
- Hemolytic anemia
- Hemolytic anemia (hereditary spherocytosis)
- Hemolytic anemia, elevated liver enzymes, and low platelet count
- Hemolytic uremic syndrome
- Hemophilia
- Hereditary spherocytosis
- High platelet count
- HL
- Hodgkin disease
- Hodgkin lymphoma
- Homozygous HbS condition
- HS (hereditary spherocytosis)
- Hughes syndrome
- HUS
- Hypercoagulability
- Hypercoagulable state
I
- IDA
- Idiopathic myelofibrosis (IMF)
- Idiopathic thrombocythemia
- Idiopathic thrombocytosis
- Immune thrombocytopenia
- Immunocytoma
- Immunodeficiency 2; IMD2
- Immunologic blood transfusion reactions
- Iron deficiency anemia
- ITP
J
L
M
- Marchiafava-Micheli syndrome
- MDS
- Mediterranean anemia
- MGUS
- Microvascular thrombosis
- MM
- Monoclonal gammopathies (evaluation of)
- Monoclonal gammopathy of undetermined significance
- Multiple myeloma
- Myelodysplastic syndrome
- Myelodysplastic syndrome (essential thrombocytosis)
- Myelofibrosis
- Myeloma
- Myelomatosis
- Myeloproliferative disorder
N
- Neutropenia (evaluation of)
- Neutropenic fever (febrile neutropenia)
- Neutrophilia (evaluation of)
- NHL
- Non-Hodgkin lymphoma
O
P
- Pancytopenia (evaluation of)
- Paroxysmal nocturnal hemoglobinuria
- Plasma cell disorder
- Plasma cell dyscrasia
- Plasma cell myeloma
- Plasmacytoid lymphocytic lymphoma
- Plasmacytoma
- PNH
- Polycythemia rubra vera
- Polycythemia vera
- Post-polycythemic myelofibrosis (PPMF)
- Post-thrombocythemic myelofibrosis (PTMF)
- Postpolycythemic myelofibrosis (PPMF)
- Posttransfusion purpura
- Precursor disease
- Primary and secondary APS
- Primary immune thrombocytopenia
- Primary myelofibrosis (PMF)
- Primary myelosclerosis
- Primary systemic amyloidosis
- Primary thrombocythemia
- Prothrombotic state
- PRV
- Pulmonary leukoagglutinin reactions
- PV (polycythemia vera)
S
- Sickle cell anemia
- Sickle cell disease (SCD)
- Sickle cell hemoglobinopathies
- Smoldering myeloma
- Splenomegaly (evaluation of)
- Systemic amyloidosis
T
- Thrombocythemia
- Thrombocytopenia (evaluation of)
- Thrombocytopenic purpura
- Thrombocytosis
- Thrombohemorrhagic disorder
- Thrombophilia
- Thrombotic thrombocytopenic purpura
- TLS
- Transfusion reaction
- Transfusion-associated graft-versus-host disease
- Transfusion-associated hemolysis
- Transfusion-related acute lung injury (TRALI)
- TTP
- Tumor lysis syndrome