MDC 16 : Diseases and disorders of blood, blood forming organs and immunologic disorders
686 Diagnosis Codes are assigned to this MDC
D74.0 Congenital methemoglobinemia
D74.8 Other methemoglobinemias
D74.9 Methemoglobinemia, unspecified
R71.0 Precipitous drop in hematocrit
R71.8 Other abnormality of red blood cells
T80.30XA ABO incompatibility reaction due to transfusion of blood or blood products, unspecified, initial encounter
T80.310A ABO incompatibility with acute hemolytic transfusion reaction, initial encounter
T80.311A ABO incompatibility with delayed hemolytic transfusion reaction, initial encounter
T80.319A ABO incompatibility with hemolytic transfusion reaction, unspecified, initial encounter
T80.39XA Other ABO incompatibility reaction due to transfusion of blood or blood products, initial encounter
T80.40XA Rh incompatibility reaction due to transfusion of blood or blood products, unspecified, initial encounter
T80.410A Rh incompatibility with acute hemolytic transfusion reaction, initial encounter
T80.411A Rh incompatibility with delayed hemolytic transfusion reaction, initial encounter
T80.419A Rh incompatibility with hemolytic transfusion reaction, unspecified, initial encounter
T80.49XA Other Rh incompatibility reaction due to transfusion of blood or blood products, initial encounter
T80.89XA Other complications following infusion, transfusion and therapeutic injection, initial encounter
T80.910A Acute hemolytic transfusion reaction, unspecified incompatibility, initial encounter
T80.911A Delayed hemolytic transfusion reaction, unspecified incompatibility, initial encounter
T80.919A Hemolytic transfusion reaction, unspecified incompatibility, unspecified as acute or delayed, initial encounter
T80.92XA Unspecified transfusion reaction, initial encounter
T80.A0XA Non-ABO incompatibility reaction due to transfusion of blood or blood products, unspecified, initial encounter
T80.A10A Non-ABO incompatibility with acute hemolytic transfusion reaction, initial encounter
T80.A11A Non-ABO incompatibility with delayed hemolytic transfusion reaction, initial encounter
T80.A19A Non-ABO incompatibility with hemolytic transfusion reaction, unspecified, initial encounter
T80.A9XA Other non-ABO incompatibility reaction due to transfusion of blood or blood products, initial encounter
D65 Disseminated intravascular coagulation [defibrination syndrome]
D66 Hereditary factor VIII deficiency
D67 Hereditary factor IX deficiency
D68.0 Von Willebrand's disease
D68.1 Hereditary factor XI deficiency
D68.2 Hereditary deficiency of other clotting factors
D68.311 Acquired hemophilia
D68.318 Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors
D68.32 Hemorrhagic disorder due to extrinsic circulating anticoagulants
D68.4 Acquired coagulation factor deficiency
D68.8 Other specified coagulation defects
D68.9 Coagulation defect, unspecified
D69.0 Allergic purpura
D69.1 Qualitative platelet defects
D69.2 Other nonthrombocytopenic purpura
D69.3 Immune thrombocytopenic purpura
D69.41 Evans syndrome
D69.42 Congenital and hereditary thrombocytopenia purpura
D69.49 Other primary thrombocytopenia
D69.51 Posttransfusion purpura
D69.59 Other secondary thrombocytopenia
D69.6 Thrombocytopenia, unspecified
D69.8 Other specified hemorrhagic conditions
D69.9 Hemorrhagic condition, unspecified
D75.82 Heparin induced thrombocytopenia (HIT)
R23.3 Spontaneous ecchymoses
A18.2 Tuberculous peripheral lymphadenopathy
A18.85 Tuberculosis of spleen
A28.1 Cat-scratch disease
D15.0 Benign neoplasm of thymus
D18.1 Lymphangioma, any site
D36.0 Benign neoplasm of lymph nodes
D3A.091 Benign carcinoid tumor of the thymus
D47.2 Monoclonal gammopathy
D47.3 Essential (hemorrhagic) thrombocythemia
D47.4 Osteomyelofibrosis
D68.312 Antiphospholipid antibody with hemorrhagic disorder
D68.51 Activated protein C resistance
D68.52 Prothrombin gene mutation
D68.59 Other primary thrombophilia
D68.61 Antiphospholipid syndrome
D68.62 Lupus anticoagulant syndrome
D68.69 Other thrombophilia
D72.10 Eosinophilia, unspecified
D72.110 Idiopathic hypereosinophilic syndrome [IHES]
D72.111 Lymphocytic Variant Hypereosinophilic Syndrome [LHES]
D72.118 Other hypereosinophilic syndrome
D72.119 Hypereosinophilic syndrome [HES], unspecified
D72.12 Drug rash with eosinophilia and systemic symptoms syndrome
D72.18 Eosinophilia in diseases classified elsewhere
D72.19 Other eosinophilia
D72.810 Lymphocytopenia
D72.818 Other decreased white blood cell count
D72.819 Decreased white blood cell count, unspecified
D72.820 Lymphocytosis (symptomatic)
D72.821 Monocytosis (symptomatic)
D72.822 Plasmacytosis
D72.823 Leukemoid reaction
D72.824 Basophilia
D72.825 Bandemia
D72.828 Other elevated white blood cell count
D72.829 Elevated white blood cell count, unspecified
D72.89 Other specified disorders of white blood cells
D72.9 Disorder of white blood cells, unspecified
D73.0 Hyposplenism
D73.1 Hypersplenism
D73.2 Chronic congestive splenomegaly
D73.3 Abscess of spleen
D73.4 Cyst of spleen
D73.5 Infarction of spleen
D73.81 Neutropenic splenomegaly
D73.89 Other diseases of spleen
D73.9 Disease of spleen, unspecified
D75.0 Familial erythrocytosis
D75.1 Secondary polycythemia