ICD-10-CM/PCS MS-DRG v39.0 Definitions Manual

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Appendix C: Principal diagnoses which convert CC/MCC to non-CC
Page 327 of 689
 
PDX Collection 3685
G20Parkinson's disease
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
G230Hallervorden-Spatz disease
G9001Carotid sinus syncope
G9009Other idiopathic peripheral autonomic neuropathy
G9340Encephalopathy, unspecified
G9341Metabolic encephalopathy
G9349Other encephalopathy
I6783Posterior reversible encephalopathy syndrome
 
PDX Collection 3687
G20Parkinson's disease
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
G231Progressive supranuclear ophthalmoplegia [Steele-Richardson-Olszewski]
G9001Carotid sinus syncope
G9009Other idiopathic peripheral autonomic neuropathy
G9340Encephalopathy, unspecified
G9341Metabolic encephalopathy
G9349Other encephalopathy
I6783Posterior reversible encephalopathy syndrome
 
PDX Collection 3689
G20Parkinson's disease
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
G232Striatonigral degeneration
G9001Carotid sinus syncope
G9009Other idiopathic peripheral autonomic neuropathy
G9340Encephalopathy, unspecified
G9341Metabolic encephalopathy
G9349Other encephalopathy
I6783Posterior reversible encephalopathy syndrome
 
PDX Collection 3691
G20Parkinson's disease
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
G238Other specified degenerative diseases of basal ganglia
G9001Carotid sinus syncope
G9009Other idiopathic peripheral autonomic neuropathy
G9340Encephalopathy, unspecified
G9341Metabolic encephalopathy
G9349Other encephalopathy
I6783Posterior reversible encephalopathy syndrome
 
PDX Collection 3693
G20Parkinson's disease
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
G239Degenerative disease of basal ganglia, unspecified
G9001Carotid sinus syncope
G9009Other idiopathic peripheral autonomic neuropathy
G9340Encephalopathy, unspecified
G9341Metabolic encephalopathy
G9349Other encephalopathy
I6783Posterior reversible encephalopathy syndrome
 
PDX Collection 3695
G20Parkinson's disease
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
G2402Drug induced acute dystonia
G2570Drug induced movement disorder, unspecified
G2571Drug induced akathisia
G2579Other drug induced movement disorders
G2589Other specified extrapyramidal and movement disorders
G259Extrapyramidal and movement disorder, unspecified
G26Extrapyramidal and movement disorders in diseases classified elsewhere
G803Athetoid cerebral palsy
G9340Encephalopathy, unspecified
G9341Metabolic encephalopathy
G9349Other encephalopathy
I6783Posterior reversible encephalopathy syndrome
 
PDX Collection 3697
G20Parkinson's disease
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
G2409Other drug induced dystonia
G2570Drug induced movement disorder, unspecified
G2571Drug induced akathisia
G2579Other drug induced movement disorders
G2589Other specified extrapyramidal and movement disorders
G259Extrapyramidal and movement disorder, unspecified
G26Extrapyramidal and movement disorders in diseases classified elsewhere
G803Athetoid cerebral palsy
G9340Encephalopathy, unspecified
G9341Metabolic encephalopathy
G9349Other encephalopathy
I6783Posterior reversible encephalopathy syndrome
 
PDX Collection 3699
G20Parkinson's disease
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
G242Idiopathic nonfamilial dystonia
G2570Drug induced movement disorder, unspecified
G2571Drug induced akathisia
G2579Other drug induced movement disorders
G2589Other specified extrapyramidal and movement disorders
G259Extrapyramidal and movement disorder, unspecified
G26Extrapyramidal and movement disorders in diseases classified elsewhere
G803Athetoid cerebral palsy
G9340Encephalopathy, unspecified
G9341Metabolic encephalopathy
G9349Other encephalopathy
I6783Posterior reversible encephalopathy syndrome
 
PDX Collection 3702
A9230West Nile virus infection, unspecified
A9231West Nile virus infection with encephalitis
A9232West Nile virus infection with other neurologic manifestation
A9239West Nile virus infection with other complications
B9721SARS-associated coronavirus as the cause of diseases classified elsewhere
G370Diffuse sclerosis of central nervous system
G9340Encephalopathy, unspecified
G9341Metabolic encephalopathy
G9349Other encephalopathy
I6783Posterior reversible encephalopathy syndrome
 
PDX Collection 3704
G210Malignant neuroleptic syndrome
G835Locked-in state
G9340Encephalopathy, unspecified
G9341Metabolic encephalopathy
G9349Other encephalopathy
 
PDX Collection 3706
C965Multifocal and unisystemic Langerhans-cell histiocytosis
C966Unifocal Langerhans-cell histiocytosis
E71310Long chain/very long chain acyl CoA dehydrogenase deficiency
E71311Medium chain acyl CoA dehydrogenase deficiency
E71312Short chain acyl CoA dehydrogenase deficiency
E71313Glutaric aciduria type II
E71314Muscle carnitine palmitoyltransferase deficiency
E71318Other disorders of fatty-acid oxidation
E7132Disorders of ketone metabolism
E7139Other disorders of fatty-acid metabolism
E7140Disorder of carnitine metabolism, unspecified
E7141Primary carnitine deficiency
E7142Carnitine deficiency due to inborn errors of metabolism
E7143Iatrogenic carnitine deficiency
E71440Ruvalcaba-Myhre-Smith syndrome
E71448Other secondary carnitine deficiency
E7150Peroxisomal disorder, unspecified
E71510Zellweger syndrome
E71511Neonatal adrenoleukodystrophy
E71518Other disorders of peroxisome biogenesis
E71520Childhood cerebral X-linked adrenoleukodystrophy
E71521Adolescent X-linked adrenoleukodystrophy
E71522Adrenomyeloneuropathy
E71528Other X-linked adrenoleukodystrophy
E71529X-linked adrenoleukodystrophy, unspecified type
E7153Other group 2 peroxisomal disorders
E71540Rhizomelic chondrodysplasia punctata
E71541Zellweger-like syndrome
E71542Other group 3 peroxisomal disorders
E71548Other peroxisomal disorders
E803Defects of catalase and peroxidase
E804Gilbert syndrome
E805Crigler-Najjar syndrome
E806Other disorders of bilirubin metabolism
E807Disorder of bilirubin metabolism, unspecified
E8889Other specified metabolic disorders
H49811Kearns-Sayre syndrome, right eye
 
PDX Collection 3708
C965Multifocal and unisystemic Langerhans-cell histiocytosis
C966Unifocal Langerhans-cell histiocytosis
E71310Long chain/very long chain acyl CoA dehydrogenase deficiency
E71311Medium chain acyl CoA dehydrogenase deficiency
E71312Short chain acyl CoA dehydrogenase deficiency
E71313Glutaric aciduria type II
E71314Muscle carnitine palmitoyltransferase deficiency
E71318Other disorders of fatty-acid oxidation
E7132Disorders of ketone metabolism
E7139Other disorders of fatty-acid metabolism
E7140Disorder of carnitine metabolism, unspecified
E7141Primary carnitine deficiency
E7142Carnitine deficiency due to inborn errors of metabolism
E7143Iatrogenic carnitine deficiency
E71440Ruvalcaba-Myhre-Smith syndrome
E71448Other secondary carnitine deficiency
E7150Peroxisomal disorder, unspecified
E71510Zellweger syndrome
E71511Neonatal adrenoleukodystrophy
E71518Other disorders of peroxisome biogenesis
E71520Childhood cerebral X-linked adrenoleukodystrophy
E71521Adolescent X-linked adrenoleukodystrophy
E71522Adrenomyeloneuropathy
E71528Other X-linked adrenoleukodystrophy
E71529X-linked adrenoleukodystrophy, unspecified type
E7153Other group 2 peroxisomal disorders
E71540Rhizomelic chondrodysplasia punctata
E71541Zellweger-like syndrome
E71542Other group 3 peroxisomal disorders
E71548Other peroxisomal disorders
E803Defects of catalase and peroxidase
E804Gilbert syndrome
E805Crigler-Najjar syndrome
E806Other disorders of bilirubin metabolism
E807Disorder of bilirubin metabolism, unspecified
E8889Other specified metabolic disorders
H49812Kearns-Sayre syndrome, left eye
 
PDX Collection 3710
C965Multifocal and unisystemic Langerhans-cell histiocytosis
C966Unifocal Langerhans-cell histiocytosis
E71310Long chain/very long chain acyl CoA dehydrogenase deficiency
E71311Medium chain acyl CoA dehydrogenase deficiency
E71312Short chain acyl CoA dehydrogenase deficiency
E71313Glutaric aciduria type II
E71314Muscle carnitine palmitoyltransferase deficiency
E71318Other disorders of fatty-acid oxidation
E7132Disorders of ketone metabolism
E7139Other disorders of fatty-acid metabolism
E7140Disorder of carnitine metabolism, unspecified
E7141Primary carnitine deficiency
E7142Carnitine deficiency due to inborn errors of metabolism
E7143Iatrogenic carnitine deficiency
E71440Ruvalcaba-Myhre-Smith syndrome
E71448Other secondary carnitine deficiency
E7150Peroxisomal disorder, unspecified
E71510Zellweger syndrome
E71511Neonatal adrenoleukodystrophy
E71518Other disorders of peroxisome biogenesis
E71520Childhood cerebral X-linked adrenoleukodystrophy
E71521Adolescent X-linked adrenoleukodystrophy
E71522Adrenomyeloneuropathy
E71528Other X-linked adrenoleukodystrophy
E71529X-linked adrenoleukodystrophy, unspecified type
E7153Other group 2 peroxisomal disorders
E71540Rhizomelic chondrodysplasia punctata
E71541Zellweger-like syndrome
E71542Other group 3 peroxisomal disorders
E71548Other peroxisomal disorders
E803Defects of catalase and peroxidase
E804Gilbert syndrome
E805Crigler-Najjar syndrome
E806Other disorders of bilirubin metabolism
E807Disorder of bilirubin metabolism, unspecified
E8889Other specified metabolic disorders
H49813Kearns-Sayre syndrome, bilateral
 
PDX Collection 3712
I0981Rheumatic heart failure
I110Hypertensive heart disease with heart failure
I130Hypertensive heart and chronic kidney disease with heart failure and stage 1 through stage 4 chronic kidney disease, or unspecified chronic kidney disease
I132Hypertensive heart and chronic kidney disease with heart failure and with stage 5 chronic kidney disease, or end stage renal disease
I200Unstable angina
I201Angina pectoris with documented spasm
I208Other 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
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
I248Other forms of acute ischemic heart disease
I249Acute ischemic heart disease, unspecified
I25110Atherosclerotic heart disease of native coronary artery with unstable angina pectoris
I255Ischemic cardiomyopathy
I256Silent myocardial ischemia
I2582Chronic total occlusion of coronary artery
I2583Coronary atherosclerosis due to lipid rich plaque
I2589Other forms of chronic ischemic heart disease
I259Chronic ischemic heart disease, unspecified
I501Left ventricular failure, unspecified
I50810Right heart failure, unspecified
I50811Acute right heart failure
I50812Chronic right heart failure
I50813Acute on chronic right heart failure
I50814Right heart failure due to left heart failure
I5082Biventricular heart failure
I5083High output heart failure
I5084End stage heart failure
I5089Other heart failure
I509Heart failure, 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 3714
I0981Rheumatic heart failure
I110Hypertensive heart disease with heart failure
I130Hypertensive heart and chronic kidney disease with heart failure and stage 1 through stage 4 chronic kidney disease, or unspecified chronic kidney disease
I132Hypertensive heart and chronic kidney disease with heart failure and with stage 5 chronic kidney disease, or end stage renal disease
I200Unstable angina
I201Angina pectoris with documented spasm
I208Other 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
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
I248Other forms of acute ischemic heart disease
I249Acute ischemic heart disease, unspecified
I255Ischemic cardiomyopathy
I256Silent myocardial ischemia
I25700Atherosclerosis of coronary artery bypass graft(s), unspecified, with unstable angina pectoris
I2582Chronic total occlusion of coronary artery
I2583Coronary atherosclerosis due to lipid rich plaque
I2589Other forms of chronic ischemic heart disease
I259Chronic ischemic heart disease, unspecified
I501Left ventricular failure, unspecified
I50810Right heart failure, unspecified
I50811Acute right heart failure
I50812Chronic right heart failure
I50813Acute on chronic right heart failure
I50814Right heart failure due to left heart failure
I5082Biventricular heart failure
I5083High output heart failure
I5084End stage heart failure
I5089Other heart failure
I509Heart failure, 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 3717
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
I25118Atherosclerotic heart disease of native coronary artery with other forms of angina pectoris
I25119Atherosclerotic heart disease of native coronary artery with unspecified angina pectoris
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
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
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
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
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
I25758Atherosclerosis of native coronary artery of transplanted heart with other forms of angina pectoris
I25759Atherosclerosis of native coronary artery of transplanted heart with unspecified angina pectoris
I25761Atherosclerosis of bypass graft of coronary artery of transplanted heart with angina pectoris with documented spasm
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
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
I25811Atherosclerosis of native coronary artery of transplanted heart without angina pectoris
I2582Chronic total occlusion of coronary artery
I2583Coronary atherosclerosis due to lipid rich plaque
I2584Coronary atherosclerosis due to calcified coronary lesion



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