ICD-10-CM/PCS MS-DRG v41.1 Definitions Manual

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Appendix C: Principal diagnoses which convert CC/MCC to non-CC
Page 53 of 429
PDX Collection 0554 (continued)
D5930Hemolytic-uremic syndrome, unspecified
D5931Infection-associated hemolytic-uremic syndrome
D5932Hereditary hemolytic-uremic syndrome
D5939Other hemolytic-uremic syndrome
D594Other nonautoimmune hemolytic anemias
D595Paroxysmal nocturnal hemoglobinuria [Marchiafava-Micheli]
D596Hemoglobinuria due to hemolysis from other external causes
D598Other acquired hemolytic anemias
D599Acquired hemolytic anemia, unspecified
D600Chronic acquired pure red cell aplasia
D601Transient acquired pure red cell aplasia
D608Other acquired pure red cell aplasias
D609Acquired pure red cell aplasia, unspecified
D6101Constitutional (pure) red blood cell aplasia
D6102Shwachman-Diamond syndrome
D6109Other constitutional aplastic anemia
D611Drug-induced aplastic anemia
D612Aplastic anemia due to other external agents
D613Idiopathic aplastic anemia
D6189Other specified aplastic anemias and other bone marrow failure syndromes
D619Aplastic anemia, unspecified
D62Acute posthemorrhagic anemia
D640Hereditary sideroblastic anemia
D642Secondary sideroblastic anemia due to drugs and toxins
D643Other sideroblastic anemias
D644Congenital dyserythropoietic anemia
D6481Anemia due to antineoplastic chemotherapy
D6489Other specified anemias
D649Anemia, unspecified
D693Immune thrombocytopenic purpura
D6941Evans syndrome
D6942Congenital and hereditary thrombocytopenia purpura
D6949Other primary thrombocytopenia
D759Disease of blood and blood-forming organs, unspecified
P612Anemia of prematurity
P613Congenital anemia from fetal blood loss
P614Other congenital anemias, not elsewhere classified
 
PDX Collection 0555
D500Iron deficiency anemia secondary to blood loss (chronic)
D501Sideropenic dysphagia
D508Other iron deficiency anemias
D509Iron deficiency anemia, unspecified
D510Vitamin B12 deficiency anemia due to intrinsic factor deficiency
D511Vitamin B12 deficiency anemia due to selective vitamin B12 malabsorption with proteinuria
D512Transcobalamin II deficiency
D513Other dietary vitamin B12 deficiency anemia
D518Other vitamin B12 deficiency anemias
D519Vitamin B12 deficiency anemia, unspecified
D520Dietary folate deficiency anemia
D521Drug-induced folate deficiency anemia
D528Other folate deficiency anemias
D529Folate deficiency anemia, unspecified
D530Protein deficiency anemia
D531Other megaloblastic anemias, not elsewhere classified
D532Scorbutic anemia
D538Other specified nutritional anemias
D539Nutritional anemia, unspecified
D550Anemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency
D551Anemia due to other disorders of glutathione metabolism
D553Anemia due to disorders of nucleotide metabolism
D558Other anemias due to enzyme disorders
D559Anemia due to enzyme disorder, unspecified
D560Alpha thalassemia
D561Beta thalassemia
D562Delta-beta thalassemia
D563Thalassemia minor
D564Hereditary persistence of fetal hemoglobin [HPFH]
D565Hemoglobin E-beta thalassemia
D568Other thalassemias
D569Thalassemia, unspecified
D5700Hb-SS disease with crisis, unspecified
D5701Hb-SS disease with acute chest syndrome
D5702Hb-SS disease with splenic sequestration
D571Sickle-cell disease without crisis
D5720Sickle-cell/Hb-C disease without crisis
D57211Sickle-cell/Hb-C disease with acute chest syndrome
D57212Sickle-cell/Hb-C disease with splenic sequestration
D57213Sickle-cell/Hb-C disease with cerebral vascular involvement
D57214Sickle-cell/Hb-C disease with dactylitis
D57218Sickle-cell/Hb-C disease with crisis with other specified complication
D57219Sickle-cell/Hb-C disease with crisis, unspecified
D573Sickle-cell trait
D5740Sickle-cell thalassemia without crisis
D57411Sickle-cell thalassemia, unspecified, with acute chest syndrome
D57412Sickle-cell thalassemia, unspecified, with splenic sequestration
D57419Sickle-cell thalassemia, unspecified, with crisis
D5780Other sickle-cell disorders without crisis
D57811Other sickle-cell disorders with acute chest syndrome
D57812Other sickle-cell disorders with splenic sequestration
D57819Other sickle-cell disorders with crisis, unspecified
D580Hereditary spherocytosis
D581Hereditary elliptocytosis
D582Other hemoglobinopathies
D588Other specified hereditary hemolytic anemias
D589Hereditary hemolytic anemia, unspecified
D590Drug-induced autoimmune hemolytic anemia
D5910Autoimmune hemolytic anemia, unspecified
D5911Warm autoimmune hemolytic anemia
D5912Cold autoimmune hemolytic anemia
D5913Mixed type autoimmune hemolytic anemia
D5919Other autoimmune hemolytic anemia
D592Drug-induced nonautoimmune hemolytic anemia
D5930Hemolytic-uremic syndrome, unspecified
D5931Infection-associated hemolytic-uremic syndrome
D5932Hereditary hemolytic-uremic syndrome
D5939Other hemolytic-uremic syndrome
D594Other nonautoimmune hemolytic anemias
D595Paroxysmal nocturnal hemoglobinuria [Marchiafava-Micheli]
D596Hemoglobinuria due to hemolysis from other external causes
D598Other acquired hemolytic anemias
D599Acquired hemolytic anemia, unspecified
D600Chronic acquired pure red cell aplasia
D601Transient acquired pure red cell aplasia
D608Other acquired pure red cell aplasias
D609Acquired pure red cell aplasia, unspecified
D6101Constitutional (pure) red blood cell aplasia
D6102Shwachman-Diamond syndrome
D6109Other constitutional aplastic anemia
D611Drug-induced aplastic anemia
D612Aplastic anemia due to other external agents
D613Idiopathic aplastic anemia
D6189Other specified aplastic anemias and other bone marrow failure syndromes
D619Aplastic anemia, unspecified
D62Acute posthemorrhagic anemia
D640Hereditary sideroblastic anemia
D642Secondary sideroblastic anemia due to drugs and toxins
D643Other sideroblastic anemias
D644Congenital dyserythropoietic anemia
D6481Anemia due to antineoplastic chemotherapy
D6489Other specified anemias
D649Anemia, unspecified
D693Immune thrombocytopenic purpura
D6941Evans syndrome
D6942Congenital and hereditary thrombocytopenia purpura
D6949Other primary thrombocytopenia
D759Disease of blood and blood-forming organs, unspecified
P612Anemia of prematurity
P613Congenital anemia from fetal blood loss
P614Other congenital anemias, not elsewhere classified
 
PDX Collection 0556
D600Chronic acquired pure red cell aplasia
D601Transient acquired pure red cell aplasia
D608Other acquired pure red cell aplasias
D609Acquired pure red cell aplasia, unspecified
D611Drug-induced aplastic anemia
D612Aplastic anemia due to other external agents
D613Idiopathic aplastic anemia
D61810Antineoplastic chemotherapy induced pancytopenia
D61811Other drug-induced pancytopenia
D61818Other pancytopenia
D6182Myelophthisis
D6189Other specified aplastic anemias and other bone marrow failure syndromes
D619Aplastic anemia, unspecified
D62Acute posthemorrhagic anemia
D640Hereditary sideroblastic anemia
D642Secondary sideroblastic anemia due to drugs and toxins
D643Other sideroblastic anemias
D644Congenital dyserythropoietic anemia
D6481Anemia due to antineoplastic chemotherapy
D6489Other specified anemias
D649Anemia, unspecified
D700Congenital agranulocytosis
D701Agranulocytosis secondary to cancer chemotherapy
D702Other drug-induced agranulocytosis
D703Neutropenia due to infection
D704Cyclic neutropenia
D708Other neutropenia
D709Neutropenia, unspecified
D72810Lymphocytopenia
D72818Other decreased white blood cell count
D72819Decreased white blood cell count, unspecified
D72820Lymphocytosis (symptomatic)
D72823Leukemoid reaction
D72825Bandemia
D72828Other elevated white blood cell count
D72829Elevated white blood cell count, unspecified
D759Disease of blood and blood-forming organs, unspecified
D761Hemophagocytic lymphohistiocytosis
D762Hemophagocytic syndrome, infection-associated
D763Other histiocytosis syndromes
P612Anemia of prematurity
 
PDX Collection 0557
D474Osteomyelofibrosis
D500Iron deficiency anemia secondary to blood loss (chronic)
D501Sideropenic dysphagia
D508Other iron deficiency anemias
D509Iron deficiency anemia, unspecified
D510Vitamin B12 deficiency anemia due to intrinsic factor deficiency
D511Vitamin B12 deficiency anemia due to selective vitamin B12 malabsorption with proteinuria
D512Transcobalamin II deficiency
D513Other dietary vitamin B12 deficiency anemia
D518Other vitamin B12 deficiency anemias
D519Vitamin B12 deficiency anemia, unspecified
D520Dietary folate deficiency anemia
D521Drug-induced folate deficiency anemia
D528Other folate deficiency anemias
D529Folate deficiency anemia, unspecified
D530Protein deficiency anemia
D531Other megaloblastic anemias, not elsewhere classified
D532Scorbutic anemia
D538Other specified nutritional anemias
D539Nutritional anemia, unspecified
D550Anemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency
D551Anemia due to other disorders of glutathione metabolism
D553Anemia due to disorders of nucleotide metabolism
D558Other anemias due to enzyme disorders
D559Anemia due to enzyme disorder, unspecified
D560Alpha thalassemia
D561Beta thalassemia
D562Delta-beta thalassemia
D563Thalassemia minor
D564Hereditary persistence of fetal hemoglobin [HPFH]
D565Hemoglobin E-beta thalassemia
D568Other thalassemias
D569Thalassemia, unspecified
D5700Hb-SS disease with crisis, unspecified
D5701Hb-SS disease with acute chest syndrome
D5702Hb-SS disease with splenic sequestration
D571Sickle-cell disease without crisis
D5720Sickle-cell/Hb-C disease without crisis
D57211Sickle-cell/Hb-C disease with acute chest syndrome
D57212Sickle-cell/Hb-C disease with splenic sequestration
D57213Sickle-cell/Hb-C disease with cerebral vascular involvement
D57214Sickle-cell/Hb-C disease with dactylitis
D57218Sickle-cell/Hb-C disease with crisis with other specified complication
D57219Sickle-cell/Hb-C disease with crisis, unspecified
D573Sickle-cell trait
D5740Sickle-cell thalassemia without crisis
D57411Sickle-cell thalassemia, unspecified, with acute chest syndrome
D57412Sickle-cell thalassemia, unspecified, with splenic sequestration
D57419Sickle-cell thalassemia, unspecified, with crisis
D5780Other sickle-cell disorders without crisis
D57811Other sickle-cell disorders with acute chest syndrome
D57812Other sickle-cell disorders with splenic sequestration
D57819Other sickle-cell disorders with crisis, unspecified
D580Hereditary spherocytosis
D581Hereditary elliptocytosis
D582Other hemoglobinopathies
D588Other specified hereditary hemolytic anemias
D589Hereditary hemolytic anemia, unspecified
D590Drug-induced autoimmune hemolytic anemia
D5910Autoimmune hemolytic anemia, unspecified
D5911Warm autoimmune hemolytic anemia
D5912Cold autoimmune hemolytic anemia
D5913Mixed type autoimmune hemolytic anemia
D5919Other autoimmune hemolytic anemia
D592Drug-induced nonautoimmune hemolytic anemia
D5930Hemolytic-uremic syndrome, unspecified
D5931Infection-associated hemolytic-uremic syndrome
D5932Hereditary hemolytic-uremic syndrome
D5939Other hemolytic-uremic syndrome
D594Other nonautoimmune hemolytic anemias
D595Paroxysmal nocturnal hemoglobinuria [Marchiafava-Micheli]
D596Hemoglobinuria due to hemolysis from other external causes
D598Other acquired hemolytic anemias
D599Acquired hemolytic anemia, unspecified
D600Chronic acquired pure red cell aplasia
D601Transient acquired pure red cell aplasia
D608Other acquired pure red cell aplasias
D609Acquired pure red cell aplasia, unspecified
D6101Constitutional (pure) red blood cell aplasia
D6102Shwachman-Diamond syndrome
D6109Other constitutional aplastic anemia
D611Drug-induced aplastic anemia
D612Aplastic anemia due to other external agents
D613Idiopathic aplastic anemia
D61810Antineoplastic chemotherapy induced pancytopenia
D61811Other drug-induced pancytopenia
D61818Other pancytopenia
D6182Myelophthisis
D6189Other specified aplastic anemias and other bone marrow failure syndromes
D619Aplastic anemia, unspecified
D62Acute posthemorrhagic anemia
D640Hereditary sideroblastic anemia
D642Secondary sideroblastic anemia due to drugs and toxins
D643Other sideroblastic anemias
D644Congenital dyserythropoietic anemia
D6481Anemia due to antineoplastic chemotherapy
D6489Other specified anemias
D649Anemia, unspecified
D68312Antiphospholipid antibody with hemorrhagic disorder
D6851Activated protein C resistance
D6852Prothrombin gene mutation
D6859Other primary thrombophilia
D6861Antiphospholipid syndrome
D6862Lupus anticoagulant syndrome
D6869Other thrombophilia
D7589Other specified diseases of blood and blood-forming organs
D759Disease of blood and blood-forming organs, unspecified
D75AGlucose-6-phosphate dehydrogenase (G6PD) deficiency without anemia
D892Hypergammaglobulinemia, unspecified
T792XXATraumatic secondary and recurrent hemorrhage and seroma, initial encounter
 
PDX Collection 0558
D474Osteomyelofibrosis
D65Disseminated intravascular coagulation [defibrination syndrome]
D66Hereditary factor VIII deficiency
D67Hereditary factor IX deficiency
D6800Von Willebrand disease, unspecified
D6801Von Willebrand disease, type 1
D68020Von Willebrand disease, type 2A
D68021Von Willebrand disease, type 2B
D68022Von Willebrand disease, type 2M
D68023Von Willebrand disease, type 2N
D68029Von Willebrand disease, type 2, unspecified
D6803Von Willebrand disease, type 3
D6804Acquired von Willebrand disease
D6809Other von Willebrand disease
D681Hereditary factor XI deficiency
D682Hereditary deficiency of other clotting factors
D68311Acquired hemophilia
D68312Antiphospholipid antibody with hemorrhagic disorder
D68318Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors
D6832Hemorrhagic disorder due to extrinsic circulating anticoagulants
D684Acquired coagulation factor deficiency
D6851Activated protein C resistance
D6852Prothrombin gene mutation
D6859Other primary thrombophilia
D6861Antiphospholipid syndrome
D6862Lupus anticoagulant syndrome
D6869Other thrombophilia
D688Other specified coagulation defects
D689Coagulation defect, unspecified
D690Allergic purpura
D691Qualitative platelet defects
D692Other nonthrombocytopenic purpura
D693Immune thrombocytopenic purpura
D6941Evans syndrome
D6942Congenital and hereditary thrombocytopenia purpura
D6949Other primary thrombocytopenia
D6951Posttransfusion purpura
D6959Other secondary thrombocytopenia
D696Thrombocytopenia, unspecified
D698Other specified hemorrhagic conditions
D699Hemorrhagic condition, unspecified
D75821Non-immune heparin-induced thrombocytopenia
D75822Immune-mediated heparin-induced thrombocytopenia
D75828Other heparin-induced thrombocytopenia syndrome
D75829Heparin-induced thrombocytopenia, unspecified
D7584Other platelet-activating anti-PF4 disorders
D7589Other specified diseases of blood and blood-forming organs
D759Disease of blood and blood-forming organs, unspecified
D75AGlucose-6-phosphate dehydrogenase (G6PD) deficiency without anemia
D892Hypergammaglobulinemia, unspecified
 
PDX Collection 0559
D474Osteomyelofibrosis
D65Disseminated intravascular coagulation [defibrination syndrome]
D66Hereditary factor VIII deficiency
D67Hereditary factor IX deficiency
D6800Von Willebrand disease, unspecified
D6801Von Willebrand disease, type 1
D68020Von Willebrand disease, type 2A
D68021Von Willebrand disease, type 2B
D68022Von Willebrand disease, type 2M
D68023Von Willebrand disease, type 2N
D68029Von Willebrand disease, type 2, unspecified
D6803Von Willebrand disease, type 3
D6804Acquired von Willebrand disease
D6809Other von Willebrand disease
D681Hereditary factor XI deficiency
D682Hereditary deficiency of other clotting factors
D68311Acquired hemophilia
D68312Antiphospholipid antibody with hemorrhagic disorder
D68318Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors
D6832Hemorrhagic disorder due to extrinsic circulating anticoagulants
D684Acquired coagulation factor deficiency
D6851Activated protein C resistance
D6852Prothrombin gene mutation
D6859Other primary thrombophilia
D6861Antiphospholipid syndrome
D6862Lupus anticoagulant syndrome
D6869Other thrombophilia
D688Other specified coagulation defects
D689Coagulation defect, unspecified
D690Allergic purpura
D691Qualitative platelet defects
D692Other nonthrombocytopenic purpura
D693Immune thrombocytopenic purpura
D6941Evans syndrome
D6942Congenital and hereditary thrombocytopenia purpura
D6949Other primary thrombocytopenia
D6951Posttransfusion purpura
D6959Other secondary thrombocytopenia
D696Thrombocytopenia, unspecified
D698Other specified hemorrhagic conditions
D699Hemorrhagic condition, unspecified
D75821Non-immune heparin-induced thrombocytopenia
D75822Immune-mediated heparin-induced thrombocytopenia
D75828Other heparin-induced thrombocytopenia syndrome
D75829Heparin-induced thrombocytopenia, unspecified
D7589Other specified diseases of blood and blood-forming organs
D759Disease of blood and blood-forming organs, unspecified
D75AGlucose-6-phosphate dehydrogenase (G6PD) deficiency without anemia
D892Hypergammaglobulinemia, unspecified
 
PDX Collection 0560
D474Osteomyelofibrosis
D6800Von Willebrand disease, unspecified
D6801Von Willebrand disease, type 1
D68020Von Willebrand disease, type 2A
D68021Von Willebrand disease, type 2B
D68022Von Willebrand disease, type 2M
D68023Von Willebrand disease, type 2N
D68029Von Willebrand disease, type 2, unspecified
D6803Von Willebrand disease, type 3
D6804Acquired von Willebrand disease
D6809Other von Willebrand disease
D68311Acquired hemophilia



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