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 1254 of 1324
PDX Collection 6835 (continued)
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
D5521Anemia due to pyruvate kinase deficiency
D5529Anemia due to other disorders of glycolytic enzymes
D553Anemia due to disorders of nucleotide metabolism
D558Other anemias due to enzyme disorders
D559Anemia due to enzyme disorder, unspecified
D564Hereditary persistence of fetal hemoglobin [HPFH]
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
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
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 6836
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
D564Hereditary persistence of fetal hemoglobin [HPFH]
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
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
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 6837
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
D564Hereditary persistence of fetal hemoglobin [HPFH]
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
D573Sickle-cell trait
D57811Other sickle-cell disorders with acute chest syndrome
D57812Other sickle-cell disorders with splenic sequestration
D57819Other sickle-cell disorders with crisis, unspecified
D582Other hemoglobinopathies
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
D5930Hemolytic-uremic syndrome, unspecified
D5931Infection-associated hemolytic-uremic syndrome
D5932Hereditary hemolytic-uremic syndrome
D5939Other hemolytic-uremic syndrome
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
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
D759Disease of blood and blood-forming organs, unspecified
P615Transient neonatal neutropenia
P618Other specified perinatal hematological disorders
P619Perinatal hematological disorder, unspecified
 
PDX Collection 6838
I200Unstable angina
I201Angina pectoris with documented spasm
I202Refractory angina pectoris
I2081Angina pectoris with coronary microvascular dysfunction
I2089Other forms of angina pectoris
I209Angina pectoris, unspecified
I2101ST elevation (STEMI) myocardial infarction involving left main coronary artery
I2102ST elevation (STEMI) myocardial infarction involving left anterior descending coronary artery
I2109ST elevation (STEMI) myocardial infarction involving other coronary artery of anterior wall
I2111ST elevation (STEMI) myocardial infarction involving right coronary artery
I2119ST elevation (STEMI) myocardial infarction involving other coronary artery of inferior wall
I2121ST elevation (STEMI) myocardial infarction involving left circumflex coronary artery
I2129ST elevation (STEMI) myocardial infarction involving other sites
I213ST elevation (STEMI) myocardial infarction of unspecified site
I214Non-ST elevation (NSTEMI) myocardial infarction
I219Acute myocardial infarction, unspecified
I21A1Myocardial infarction type 2
I21A9Other myocardial infarction type
I21BMyocardial infarction with coronary microvascular dysfunction
I220Subsequent ST elevation (STEMI) myocardial infarction of anterior wall
I221Subsequent ST elevation (STEMI) myocardial infarction of inferior wall
I222Subsequent non-ST elevation (NSTEMI) myocardial infarction
I228Subsequent ST elevation (STEMI) myocardial infarction of other sites
I229Subsequent ST elevation (STEMI) myocardial infarction of unspecified site
I240Acute coronary thrombosis not resulting in myocardial infarction
I2481Acute coronary microvascular dysfunction
I2489Other forms of acute ischemic heart disease
I249Acute ischemic heart disease, unspecified
I2510Atherosclerotic heart disease of native coronary artery without angina pectoris
I25110Atherosclerotic heart disease of native coronary artery with unstable angina pectoris
I25111Atherosclerotic heart disease of native coronary artery with angina pectoris with documented spasm
I25112Atherosclerotic heart disease of native coronary artery with refractory angina pectoris
I25118Atherosclerotic heart disease of native coronary artery with other forms of angina pectoris
I25119Atherosclerotic heart disease of native coronary artery with unspecified angina pectoris
I255Ischemic cardiomyopathy
I256Silent myocardial ischemia
I25700Atherosclerosis of coronary artery bypass graft(s), unspecified, with unstable angina pectoris
I25701Atherosclerosis of coronary artery bypass graft(s), unspecified, with angina pectoris with documented spasm
I25702Atherosclerosis of coronary artery bypass graft(s), unspecified, with refractory angina pectoris
I25708Atherosclerosis of coronary artery bypass graft(s), unspecified, with other forms of angina pectoris
I25709Atherosclerosis of coronary artery bypass graft(s), unspecified, with unspecified angina pectoris
I25710Atherosclerosis of autologous vein coronary artery bypass graft(s) with unstable angina pectoris
I25711Atherosclerosis of autologous vein coronary artery bypass graft(s) with angina pectoris with documented spasm
I25712Atherosclerosis of autologous vein coronary artery bypass graft(s) with refractory angina pectoris
I25718Atherosclerosis of autologous vein coronary artery bypass graft(s) with other forms of angina pectoris
I25719Atherosclerosis of autologous vein coronary artery bypass graft(s) with unspecified angina pectoris
I25720Atherosclerosis of autologous artery coronary artery bypass graft(s) with unstable angina pectoris
I25721Atherosclerosis of autologous artery coronary artery bypass graft(s) with angina pectoris with documented spasm
I25722Atherosclerosis of autologous artery coronary artery bypass graft(s) with refractory angina pectoris
I25728Atherosclerosis of autologous artery coronary artery bypass graft(s) with other forms of angina pectoris
I25729Atherosclerosis of autologous artery coronary artery bypass graft(s) with unspecified angina pectoris
I25730Atherosclerosis of nonautologous biological coronary artery bypass graft(s) with unstable angina pectoris
I25731Atherosclerosis of nonautologous biological coronary artery bypass graft(s) with angina pectoris with documented spasm
I25732Atherosclerosis of nonautologous biological coronary artery bypass graft(s) with refractory angina pectoris
I25738Atherosclerosis of nonautologous biological coronary artery bypass graft(s) with other forms of angina pectoris
I25739Atherosclerosis of nonautologous biological coronary artery bypass graft(s) with unspecified angina pectoris
I25750Atherosclerosis of native coronary artery of transplanted heart with unstable angina
I25751Atherosclerosis of native coronary artery of transplanted heart with angina pectoris with documented spasm
I25752Atherosclerosis of native coronary artery of transplanted heart with refractory angina pectoris
I25759Atherosclerosis of native coronary artery of transplanted heart with unspecified angina pectoris
I25760Atherosclerosis of bypass graft of coronary artery of transplanted heart with unstable angina
I25761Atherosclerosis of bypass graft of coronary artery of transplanted heart with angina pectoris with documented spasm
I25762Atherosclerosis of bypass graft of coronary artery of transplanted heart with refractory angina pectoris
I25768Atherosclerosis of bypass graft of coronary artery of transplanted heart with other forms of angina pectoris
I25769Atherosclerosis of bypass graft of coronary artery of transplanted heart with unspecified angina pectoris
I25790Atherosclerosis of other coronary artery bypass graft(s) with unstable angina pectoris
I25791Atherosclerosis of other coronary artery bypass graft(s) with angina pectoris with documented spasm
I25792Atherosclerosis of other coronary artery bypass graft(s) with refractory angina pectoris
I25798Atherosclerosis of other coronary artery bypass graft(s) with other forms of angina pectoris
I25799Atherosclerosis of other coronary artery bypass graft(s) with unspecified angina pectoris
I25812Atherosclerosis of bypass graft of coronary artery of transplanted heart without angina pectoris
I2585Chronic coronary microvascular dysfunction
I2589Other forms of chronic ischemic heart disease
I259Chronic ischemic heart disease, unspecified
I878Other specified disorders of veins
I879Disorder of vein, unspecified
I998Other disorder of circulatory system
I999Unspecified disorder of circulatory system
R570Cardiogenic shock
R579Shock, unspecified
 
PDX Collection 6839
G802Spastic hemiplegic cerebral palsy
G9340Encephalopathy, unspecified
G9341Metabolic encephalopathy
G9342Megaloencephalic leukoencephalopathy with subcortical cysts
G9343Leukoencephalopathy with calcifications and cysts
G9344Adult-onset leukodystrophy with axonal spheroids
G9349Other encephalopathy
I6783Posterior reversible encephalopathy syndrome
 
PDX Collection 6840
G801Spastic diplegic cerebral palsy
G9340Encephalopathy, unspecified
G9341Metabolic encephalopathy
G9342Megaloencephalic leukoencephalopathy with subcortical cysts
G9343Leukoencephalopathy with calcifications and cysts
G9344Adult-onset leukodystrophy with axonal spheroids
G9349Other encephalopathy
I6783Posterior reversible encephalopathy syndrome
 
PDX Collection 6841
G20A1Parkinson's disease without dyskinesia, without mention of fluctuations
G20A2Parkinson's disease without dyskinesia, with fluctuations
G20B1Parkinson's disease with dyskinesia, without mention of fluctuations
G20B2Parkinson's disease with dyskinesia, with fluctuations
G20CParkinsonism, unspecified
G2111Neuroleptic induced parkinsonism
G2119Other drug induced secondary parkinsonism
G212Secondary parkinsonism due to other external agents
G213Postencephalitic parkinsonism
G214Vascular parkinsonism
G218Other secondary parkinsonism
G219Secondary parkinsonism, unspecified
G2570Drug induced movement disorder, unspecified
G2571Drug induced akathisia
G2579Other drug induced movement disorders
G2589Other specified extrapyramidal and movement disorders
G259Extrapyramidal and movement disorder, unspecified
G800Spastic quadriplegic cerebral palsy
G801Spastic diplegic cerebral palsy
G802Spastic hemiplegic cerebral palsy
G803Athetoid cerebral palsy
G804Ataxic cerebral palsy
G808Other cerebral palsy
G809Cerebral palsy, unspecified
G9340Encephalopathy, unspecified
G9341Metabolic encephalopathy
G9342Megaloencephalic leukoencephalopathy with subcortical cysts
G9343Leukoencephalopathy with calcifications and cysts
G9344Adult-onset leukodystrophy with axonal spheroids
G9349Other encephalopathy
I6783Posterior reversible encephalopathy syndrome
 
PDX Collection 6842
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



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13 Oct 2023 12:52:35
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