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ICD-10-CM/PCS MS-DRG v41.0 Definitions Manual |
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Appendix C: Principal diagnoses which convert CC/MCC to non-CC |
Page 1332 of 1375 |
PDX Collection 6913 (continued) | |
N80A51 | Deep endometriosis of right ureter |
N80A52 | Deep endometriosis of left ureter |
N80A53 | Deep endometriosis of bilateral ureters |
N80A59 | Deep endometriosis of unspecified ureter |
N80A61 | Endometriosis of right ureter, unspecified depth |
N80A62 | Endometriosis of left ureter, unspecified depth |
N80A63 | Endometriosis of bilateral ureters, unspecified depth |
N80A69 | Endometriosis of unspecified ureter, unspecified depth |
R310 | Gross hematuria |
R311 | Benign essential microscopic hematuria |
R3121 | Asymptomatic microscopic hematuria |
R3129 | Other microscopic hematuria |
R319 | Hematuria, unspecified |
PDX Collection 6914 | |
D474 | Osteomyelofibrosis |
D500 | Iron deficiency anemia secondary to blood loss (chronic) |
D501 | Sideropenic dysphagia |
D508 | Other iron deficiency anemias |
D509 | Iron deficiency anemia, unspecified |
D510 | Vitamin B12 deficiency anemia due to intrinsic factor deficiency |
D511 | Vitamin B12 deficiency anemia due to selective vitamin B12 malabsorption with proteinuria |
D512 | Transcobalamin II deficiency |
D513 | Other dietary vitamin B12 deficiency anemia |
D518 | Other vitamin B12 deficiency anemias |
D519 | Vitamin B12 deficiency anemia, unspecified |
D520 | Dietary folate deficiency anemia |
D521 | Drug-induced folate deficiency anemia |
D528 | Other folate deficiency anemias |
D529 | Folate deficiency anemia, unspecified |
D530 | Protein deficiency anemia |
D531 | Other megaloblastic anemias, not elsewhere classified |
D532 | Scorbutic anemia |
D538 | Other specified nutritional anemias |
D539 | Nutritional anemia, unspecified |
D550 | Anemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency |
D551 | Anemia due to other disorders of glutathione metabolism |
D553 | Anemia due to disorders of nucleotide metabolism |
D558 | Other anemias due to enzyme disorders |
D559 | Anemia due to enzyme disorder, unspecified |
D560 | Alpha thalassemia |
D561 | Beta thalassemia |
D562 | Delta-beta thalassemia |
D563 | Thalassemia minor |
D564 | Hereditary persistence of fetal hemoglobin [HPFH] |
D565 | Hemoglobin E-beta thalassemia |
D568 | Other thalassemias |
D569 | Thalassemia, unspecified |
D5700 | Hb-SS disease with crisis, unspecified |
D5701 | Hb-SS disease with acute chest syndrome |
D5702 | Hb-SS disease with splenic sequestration |
D571 | Sickle-cell disease without crisis |
D5720 | Sickle-cell/Hb-C disease without crisis |
D57211 | Sickle-cell/Hb-C disease with acute chest syndrome |
D57212 | Sickle-cell/Hb-C disease with splenic sequestration |
D57213 | Sickle-cell/Hb-C disease with cerebral vascular involvement |
D57214 | Sickle-cell/Hb-C disease with dactylitis |
D57218 | Sickle-cell/Hb-C disease with crisis with other specified complication |
D57219 | Sickle-cell/Hb-C disease with crisis, unspecified |
D573 | Sickle-cell trait |
D5740 | Sickle-cell thalassemia without crisis |
D57411 | Sickle-cell thalassemia, unspecified, with acute chest syndrome |
D57412 | Sickle-cell thalassemia, unspecified, with splenic sequestration |
D57419 | Sickle-cell thalassemia, unspecified, with crisis |
D5780 | Other sickle-cell disorders without crisis |
D57811 | Other sickle-cell disorders with acute chest syndrome |
D57812 | Other sickle-cell disorders with splenic sequestration |
D57819 | Other sickle-cell disorders with crisis, unspecified |
D580 | Hereditary spherocytosis |
D581 | Hereditary elliptocytosis |
D582 | Other hemoglobinopathies |
D588 | Other specified hereditary hemolytic anemias |
D589 | Hereditary hemolytic anemia, unspecified |
D590 | Drug-induced autoimmune hemolytic anemia |
D5910 | Autoimmune hemolytic anemia, unspecified |
D5911 | Warm autoimmune hemolytic anemia |
D5912 | Cold autoimmune hemolytic anemia |
D5913 | Mixed type autoimmune hemolytic anemia |
D5919 | Other autoimmune hemolytic anemia |
D592 | Drug-induced nonautoimmune hemolytic anemia |
D5930 | Hemolytic-uremic syndrome, unspecified |
D5931 | Infection-associated hemolytic-uremic syndrome |
D5932 | Hereditary hemolytic-uremic syndrome |
D5939 | Other hemolytic-uremic syndrome |
D594 | Other nonautoimmune hemolytic anemias |
D595 | Paroxysmal nocturnal hemoglobinuria [Marchiafava-Micheli] |
D596 | Hemoglobinuria due to hemolysis from other external causes |
D598 | Other acquired hemolytic anemias |
D599 | Acquired hemolytic anemia, unspecified |
D600 | Chronic acquired pure red cell aplasia |
D601 | Transient acquired pure red cell aplasia |
D608 | Other acquired pure red cell aplasias |
D609 | Acquired pure red cell aplasia, unspecified |
D6101 | Constitutional (pure) red blood cell aplasia |
D6102 | Shwachman-Diamond syndrome |
D6109 | Other constitutional aplastic anemia |
D611 | Drug-induced aplastic anemia |
D612 | Aplastic anemia due to other external agents |
D613 | Idiopathic aplastic anemia |
D61810 | Antineoplastic chemotherapy induced pancytopenia |
D61811 | Other drug-induced pancytopenia |
D61818 | Other pancytopenia |
D6182 | Myelophthisis |
D6189 | Other specified aplastic anemias and other bone marrow failure syndromes |
D619 | Aplastic anemia, unspecified |
D62 | Acute posthemorrhagic anemia |
D630 | Anemia in neoplastic disease |
D631 | Anemia in chronic kidney disease |
D638 | Anemia in other chronic diseases classified elsewhere |
D640 | Hereditary sideroblastic anemia |
D641 | Secondary sideroblastic anemia due to disease |
D642 | Secondary sideroblastic anemia due to drugs and toxins |
D643 | Other sideroblastic anemias |
D644 | Congenital dyserythropoietic anemia |
D6481 | Anemia due to antineoplastic chemotherapy |
D6489 | Other specified anemias |
D649 | Anemia, unspecified |
D68312 | Antiphospholipid antibody with hemorrhagic disorder |
D6851 | Activated protein C resistance |
D6852 | Prothrombin gene mutation |
D6859 | Other primary thrombophilia |
D6861 | Antiphospholipid syndrome |
D6862 | Lupus anticoagulant syndrome |
D6869 | Other thrombophilia |
D7581 | Myelofibrosis |
D7589 | Other specified diseases of blood and blood-forming organs |
D759 | Disease of blood and blood-forming organs, unspecified |
D75A | Glucose-6-phosphate dehydrogenase (G6PD) deficiency without anemia |
D77 | Other disorders of blood and blood-forming organs in diseases classified elsewhere |
D892 | Hypergammaglobulinemia, unspecified |
PDX Collection 6915 | |
D474 | Osteomyelofibrosis |
D500 | Iron deficiency anemia secondary to blood loss (chronic) |
D501 | Sideropenic dysphagia |
D508 | Other iron deficiency anemias |
D509 | Iron deficiency anemia, unspecified |
D510 | Vitamin B12 deficiency anemia due to intrinsic factor deficiency |
D511 | Vitamin B12 deficiency anemia due to selective vitamin B12 malabsorption with proteinuria |
D512 | Transcobalamin II deficiency |
D513 | Other dietary vitamin B12 deficiency anemia |
D518 | Other vitamin B12 deficiency anemias |
D519 | Vitamin B12 deficiency anemia, unspecified |
D520 | Dietary folate deficiency anemia |
D521 | Drug-induced folate deficiency anemia |
D528 | Other folate deficiency anemias |
D529 | Folate deficiency anemia, unspecified |
D530 | Protein deficiency anemia |
D531 | Other megaloblastic anemias, not elsewhere classified |
D532 | Scorbutic anemia |
D538 | Other specified nutritional anemias |
D539 | Nutritional anemia, unspecified |
D550 | Anemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency |
D551 | Anemia due to other disorders of glutathione metabolism |
D553 | Anemia due to disorders of nucleotide metabolism |
D558 | Other anemias due to enzyme disorders |
D559 | Anemia due to enzyme disorder, unspecified |
D560 | Alpha thalassemia |
D561 | Beta thalassemia |
D562 | Delta-beta thalassemia |
D563 | Thalassemia minor |
D564 | Hereditary persistence of fetal hemoglobin [HPFH] |
D565 | Hemoglobin E-beta thalassemia |
D568 | Other thalassemias |
D569 | Thalassemia, unspecified |
D5700 | Hb-SS disease with crisis, unspecified |
D5701 | Hb-SS disease with acute chest syndrome |
D5702 | Hb-SS disease with splenic sequestration |
D571 | Sickle-cell disease without crisis |
D5720 | Sickle-cell/Hb-C disease without crisis |
D57211 | Sickle-cell/Hb-C disease with acute chest syndrome |
D57212 | Sickle-cell/Hb-C disease with splenic sequestration |
D57213 | Sickle-cell/Hb-C disease with cerebral vascular involvement |
D57214 | Sickle-cell/Hb-C disease with dactylitis |
D57218 | Sickle-cell/Hb-C disease with crisis with other specified complication |
D57219 | Sickle-cell/Hb-C disease with crisis, unspecified |
D573 | Sickle-cell trait |
D5740 | Sickle-cell thalassemia without crisis |
D57411 | Sickle-cell thalassemia, unspecified, with acute chest syndrome |
D57412 | Sickle-cell thalassemia, unspecified, with splenic sequestration |
D57419 | Sickle-cell thalassemia, unspecified, with crisis |
D5780 | Other sickle-cell disorders without crisis |
D57811 | Other sickle-cell disorders with acute chest syndrome |
D57812 | Other sickle-cell disorders with splenic sequestration |
D57819 | Other sickle-cell disorders with crisis, unspecified |
D580 | Hereditary spherocytosis |
D581 | Hereditary elliptocytosis |
D582 | Other hemoglobinopathies |
D588 | Other specified hereditary hemolytic anemias |
D589 | Hereditary hemolytic anemia, unspecified |
D590 | Drug-induced autoimmune hemolytic anemia |
D5910 | Autoimmune hemolytic anemia, unspecified |
D5911 | Warm autoimmune hemolytic anemia |
D5912 | Cold autoimmune hemolytic anemia |
D5913 | Mixed type autoimmune hemolytic anemia |
D5919 | Other autoimmune hemolytic anemia |
D592 | Drug-induced nonautoimmune hemolytic anemia |
D5930 | Hemolytic-uremic syndrome, unspecified |
D5931 | Infection-associated hemolytic-uremic syndrome |
D5932 | Hereditary hemolytic-uremic syndrome |
D5939 | Other hemolytic-uremic syndrome |
D594 | Other nonautoimmune hemolytic anemias |
D595 | Paroxysmal nocturnal hemoglobinuria [Marchiafava-Micheli] |
D596 | Hemoglobinuria due to hemolysis from other external causes |
D598 | Other acquired hemolytic anemias |
D599 | Acquired hemolytic anemia, unspecified |
D600 | Chronic acquired pure red cell aplasia |
D601 | Transient acquired pure red cell aplasia |
D608 | Other acquired pure red cell aplasias |
D609 | Acquired pure red cell aplasia, unspecified |
D6101 | Constitutional (pure) red blood cell aplasia |
D6102 | Shwachman-Diamond syndrome |
D6109 | Other constitutional aplastic anemia |
D611 | Drug-induced aplastic anemia |
D612 | Aplastic anemia due to other external agents |
D613 | Idiopathic aplastic anemia |
D61810 | Antineoplastic chemotherapy induced pancytopenia |
D61811 | Other drug-induced pancytopenia |
D61818 | Other pancytopenia |
D6182 | Myelophthisis |
D6189 | Other specified aplastic anemias and other bone marrow failure syndromes |
D619 | Aplastic anemia, unspecified |
D62 | Acute posthemorrhagic anemia |
D630 | Anemia in neoplastic disease |
D631 | Anemia in chronic kidney disease |
D638 | Anemia in other chronic diseases classified elsewhere |
D640 | Hereditary sideroblastic anemia |
D641 | Secondary sideroblastic anemia due to disease |
D642 | Secondary sideroblastic anemia due to drugs and toxins |
D643 | Other sideroblastic anemias |
D644 | Congenital dyserythropoietic anemia |
D6481 | Anemia due to antineoplastic chemotherapy |
D6489 | Other specified anemias |
D649 | Anemia, unspecified |
D68312 | Antiphospholipid antibody with hemorrhagic disorder |
D6851 | Activated protein C resistance |
D6852 | Prothrombin gene mutation |
D6859 | Other primary thrombophilia |
D6861 | Antiphospholipid syndrome |
D6862 | Lupus anticoagulant syndrome |
D6869 | Other thrombophilia |
D7581 | Myelofibrosis |
D7589 | Other specified diseases of blood and blood-forming organs |
D759 | Disease of blood and blood-forming organs, unspecified |
D75A | Glucose-6-phosphate dehydrogenase (G6PD) deficiency without anemia |
D77 | Other disorders of blood and blood-forming organs in diseases classified elsewhere |
D892 | Hypergammaglobulinemia, unspecified |
PDX Collection 6916 | |
D474 | Osteomyelofibrosis |
D500 | Iron deficiency anemia secondary to blood loss (chronic) |
D501 | Sideropenic dysphagia |
D508 | Other iron deficiency anemias |
D509 | Iron deficiency anemia, unspecified |
D510 | Vitamin B12 deficiency anemia due to intrinsic factor deficiency |
D511 | Vitamin B12 deficiency anemia due to selective vitamin B12 malabsorption with proteinuria |
D512 | Transcobalamin II deficiency |
D513 | Other dietary vitamin B12 deficiency anemia |
D518 | Other vitamin B12 deficiency anemias |
D519 | Vitamin B12 deficiency anemia, unspecified |
D520 | Dietary folate deficiency anemia |
D521 | Drug-induced folate deficiency anemia |
D528 | Other folate deficiency anemias |
D529 | Folate deficiency anemia, unspecified |
D530 | Protein deficiency anemia |
D531 | Other megaloblastic anemias, not elsewhere classified |
D532 | Scorbutic anemia |
D538 | Other specified nutritional anemias |
D539 | Nutritional anemia, unspecified |
D550 | Anemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency |
D551 | Anemia due to other disorders of glutathione metabolism |
D5521 | Anemia due to pyruvate kinase deficiency |
D5529 | Anemia due to other disorders of glycolytic enzymes |
D553 | Anemia due to disorders of nucleotide metabolism |
D558 | Other anemias due to enzyme disorders |
D559 | Anemia due to enzyme disorder, unspecified |
D560 | Alpha thalassemia |
D561 | Beta thalassemia |
D562 | Delta-beta thalassemia |
D563 | Thalassemia minor |
D564 | Hereditary persistence of fetal hemoglobin [HPFH] |
D565 | Hemoglobin E-beta thalassemia |
D568 | Other thalassemias |
D569 | Thalassemia, unspecified |
D5700 | Hb-SS disease with crisis, unspecified |
D5701 | Hb-SS disease with acute chest syndrome |
D5702 | Hb-SS disease with splenic sequestration |
D571 | Sickle-cell disease without crisis |
D5720 | Sickle-cell/Hb-C disease without crisis |
D57211 | Sickle-cell/Hb-C disease with acute chest syndrome |
D57212 | Sickle-cell/Hb-C disease with splenic sequestration |
D57213 | Sickle-cell/Hb-C disease with cerebral vascular involvement |
D57214 | Sickle-cell/Hb-C disease with dactylitis |
D57218 | Sickle-cell/Hb-C disease with crisis with other specified complication |
D57219 | Sickle-cell/Hb-C disease with crisis, unspecified |
D573 | Sickle-cell trait |
D5740 | Sickle-cell thalassemia without crisis |
D57411 | Sickle-cell thalassemia, unspecified, with acute chest syndrome |
D57412 | Sickle-cell thalassemia, unspecified, with splenic sequestration |
D57419 | Sickle-cell thalassemia, unspecified, with crisis |
D5780 | Other sickle-cell disorders without crisis |
D57811 | Other sickle-cell disorders with acute chest syndrome |
D57812 | Other sickle-cell disorders with splenic sequestration |
D57819 | Other sickle-cell disorders with crisis, unspecified |
D580 | Hereditary spherocytosis |
D581 | Hereditary elliptocytosis |
D582 | Other hemoglobinopathies |
D588 | Other specified hereditary hemolytic anemias |
D589 | Hereditary hemolytic anemia, unspecified |
D590 | Drug-induced autoimmune hemolytic anemia |
D5910 | Autoimmune hemolytic anemia, unspecified |
D5911 | Warm autoimmune hemolytic anemia |
D5912 | Cold autoimmune hemolytic anemia |
D5913 | Mixed type autoimmune hemolytic anemia |
D5919 | Other autoimmune hemolytic anemia |
D592 | Drug-induced nonautoimmune hemolytic anemia |
D5930 | Hemolytic-uremic syndrome, unspecified |
D5931 | Infection-associated hemolytic-uremic syndrome |
D5932 | Hereditary hemolytic-uremic syndrome |
D5939 | Other hemolytic-uremic syndrome |
D594 | Other nonautoimmune hemolytic anemias |
D595 | Paroxysmal nocturnal hemoglobinuria [Marchiafava-Micheli] |
D596 | Hemoglobinuria due to hemolysis from other external causes |
D598 | Other acquired hemolytic anemias |
D599 | Acquired hemolytic anemia, unspecified |
D600 | Chronic acquired pure red cell aplasia |
D601 | Transient acquired pure red cell aplasia |
D608 | Other acquired pure red cell aplasias |
D609 | Acquired pure red cell aplasia, unspecified |
D6101 | Constitutional (pure) red blood cell aplasia |
D6102 | Shwachman-Diamond syndrome |
D6109 | Other constitutional aplastic anemia |
D611 | Drug-induced aplastic anemia |
D612 | Aplastic anemia due to other external agents |
D613 | Idiopathic aplastic anemia |
D61810 | Antineoplastic chemotherapy induced pancytopenia |
D61811 | Other drug-induced pancytopenia |
D61818 | Other pancytopenia |
D6182 | Myelophthisis |
D6189 | Other specified aplastic anemias and other bone marrow failure syndromes |
D619 | Aplastic anemia, unspecified |
D62 | Acute posthemorrhagic anemia |
D630 | Anemia in neoplastic disease |
D631 | Anemia in chronic kidney disease |
D638 | Anemia in other chronic diseases classified elsewhere |
D640 | Hereditary sideroblastic anemia |
D641 | Secondary sideroblastic anemia due to disease |
D642 | Secondary sideroblastic anemia due to drugs and toxins |
D643 | Other sideroblastic anemias |
D644 | Congenital dyserythropoietic anemia |
D6481 | Anemia due to antineoplastic chemotherapy |
D6489 | Other specified anemias |
D649 | Anemia, unspecified |
D68312 | Antiphospholipid antibody with hemorrhagic disorder |
D6851 | Activated protein C resistance |
D6852 | Prothrombin gene mutation |
D6859 | Other primary thrombophilia |
D6861 | Antiphospholipid syndrome |
D6862 | Lupus anticoagulant syndrome |
D6869 | Other thrombophilia |
D7581 | Myelofibrosis |
D7589 | Other specified diseases of blood and blood-forming organs |
D759 | Disease of blood and blood-forming organs, unspecified |
D75A | Glucose-6-phosphate dehydrogenase (G6PD) deficiency without anemia |
D77 | Other disorders of blood and blood-forming organs in diseases classified elsewhere |
D892 | Hypergammaglobulinemia, unspecified |
PDX Collection 6917 | |
N000 | Acute nephritic syndrome with minor glomerular abnormality |
N001 | Acute nephritic syndrome with focal and segmental glomerular lesions |
N002 | Acute nephritic syndrome with diffuse membranous glomerulonephritis |
N003 | Acute nephritic syndrome with diffuse mesangial proliferative glomerulonephritis |
N004 | Acute nephritic syndrome with diffuse endocapillary proliferative glomerulonephritis |
N005 | Acute nephritic syndrome with diffuse mesangiocapillary glomerulonephritis |
N006 | Acute nephritic syndrome with dense deposit disease |
N007 | Acute nephritic syndrome with diffuse crescentic glomerulonephritis |
N008 | Acute nephritic syndrome with other morphologic changes |
N009 | Acute nephritic syndrome with unspecified morphologic changes |
N00A | Acute nephritic syndrome with C3 glomerulonephritis |
N010 | Rapidly progressive nephritic syndrome with minor glomerular abnormality |
N011 | Rapidly progressive nephritic syndrome with focal and segmental glomerular lesions |
N012 | Rapidly progressive nephritic syndrome with diffuse membranous glomerulonephritis |
N013 | Rapidly progressive nephritic syndrome with diffuse mesangial proliferative glomerulonephritis |
N014 | Rapidly progressive nephritic syndrome with diffuse endocapillary proliferative glomerulonephritis |
N015 | Rapidly progressive nephritic syndrome with diffuse mesangiocapillary glomerulonephritis |
N016 | Rapidly progressive nephritic syndrome with dense deposit disease |
N017 | Rapidly progressive nephritic syndrome with diffuse crescentic glomerulonephritis |
N018 | Rapidly progressive nephritic syndrome with other morphologic changes |
N019 | Rapidly progressive nephritic syndrome with unspecified morphologic changes |
N01A | Rapidly progressive nephritic syndrome with C3 glomerulonephritis |
N020 | Recurrent and persistent hematuria with minor glomerular abnormality |
N021 | Recurrent and persistent hematuria with focal and segmental glomerular lesions |
N022 | Recurrent and persistent hematuria with diffuse membranous glomerulonephritis |
N023 | Recurrent and persistent hematuria with diffuse mesangial proliferative glomerulonephritis |
N024 | Recurrent and persistent hematuria with diffuse endocapillary proliferative glomerulonephritis |
N025 | Recurrent and persistent hematuria with diffuse mesangiocapillary glomerulonephritis |
N026 | Recurrent and persistent hematuria with dense deposit disease |
N027 | Recurrent and persistent hematuria with diffuse crescentic glomerulonephritis |
N028 | Recurrent and persistent hematuria with other morphologic changes |
N029 | Recurrent and persistent hematuria with unspecified morphologic changes |
N02A | Recurrent and persistent hematuria with C3 glomerulonephritis |
N02B1 | Recurrent and persistent immunoglobulin A nephropathy with glomerular lesion |
N02B2 | Recurrent and persistent immunoglobulin A nephropathy with focal and segmental glomerular lesion |
N02B3 | Recurrent and persistent immunoglobulin A nephropathy with diffuse membranoproliferative glomerulonephritis |
N02B4 | Recurrent and persistent immunoglobulin A nephropathy with diffuse membranous glomerulonephritis |
N02B5 | Recurrent and persistent immunoglobulin A nephropathy with diffuse mesangial proliferative glomerulonephritis |
N02B6 | Recurrent and persistent immunoglobulin A nephropathy with diffuse mesangiocapillary glomerulonephritis |
N02B9 | Other recurrent and persistent immunoglobulin A nephropathy |
N030 | Chronic nephritic syndrome with minor glomerular abnormality |
Centers for Medicare & Medicaid Services, 7500 Security Boulevard Baltimore, MD 21244 01 Mar 2023 06:12:40 CMS, code-revision=344, description-revision=1357 |