ICD-10 Search Results for diseases-of-blood-forming-organs-certain-disorders-involving-immune-mechanism


ICD-10-CM CodeDescriptionCategoryValid for Submission
O99.1Other diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism complicating pregnancy, childbirth and the puerperiumNot Valid
O99.11Other diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism complicating pregnancyNot Valid
O99.111Other diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism complicating pregnancy, first trimesterValid
O99.112Other diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism complicating pregnancy, second trimesterValid
O99.113Other diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism complicating pregnancy, third trimesterValid
O99.119Other diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism complicating pregnancy, unspecified trimester
Blood coagulation disorder complicating pregnancy;
Valid
O99.12Other diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism complicating childbirth
Blood coagulation disorder complicating childbirth;
Valid
O99.13Other diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism complicating the puerperiumValid
Z13.0Encounter for screening for diseases of the blood and blood-forming organs and certain disorders involving the immune mechanismValid
Z83.2Family history of diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
Family history of blood coagulation disorder; Family history of antithrombin III deficiency; Family history of protein S deficiency; Family history of protein C deficiency; Family history of protein C resistance; Family history of hypercoagulable state; Family history of Factor V Leiden mutation; Family history of sickle cell anemia; Family history of factor V deficiency; Family history of disorder due to sex chromosome abnormality; Family history of pernicious anemia; Family history of antiphospholipid syndrome; Family history of asplenia; Family history of polycythemia; Family history of rheumatic fever; Family history of sarcoidosis; Family history of immunodeficiency disorder; Family history of congenital immunodeficiency disease; Family history of beta thalassemia; Family history of hemoglobinopathy C; Family history of hemoglobinopathy E; Family history of alpha thalassemia; Family history of hemoglobinopathy; Family history of Von Willebrand disease; Family history of hemophilia A; Family history of disorder of immune function; Family history of blood coagulation disorder; FH: Blood disorder; FH: Autoimmune disease; Family history of disorder of immune function;
Valid
Z86.2Personal history of diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
History of pre-eclampsia; History of immune disorder; History of anemia vitamin B12 deficient; History of hemolytic anemia; History of hemolytic disease; History of anemia; History of lymphadenopathy; History of aplastic anemia; History of autoimmune hemolytic anemia; History of sickle cell anemia; History of splenomegaly; History of immune thrombocytopenia; History of Fanconi anemia; History of Diamond-Blackfan anemia; History of thrombophilia; History of lymphocytosis; History of immunodeficiency disorder; History of histiocytosis; History of neutropenia; History of thrombocytopenia; History of patient immunocompromised; History of gestational hypertension; History of hemolysis-elevated liver enzymes-low platelet count syndrome; History of hypercoagulable state; H/O: blood disorder; History of immune disorder; History of autoimmune hemolytic anemia; History of immune thrombocytopenia;
Valid