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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 1292 of 1375
PDX Collection 6776 (continued)
Q969Turner's syndrome, unspecified
Q970Karyotype 47, XXX
Q971Female with more than three X chromosomes
Q972Mosaicism, lines with various numbers of X chromosomes
Q973Female with 46, XY karyotype
Q978Other specified sex chromosome abnormalities, female phenotype
Q979Sex chromosome abnormality, female phenotype, unspecified
Q980Klinefelter syndrome karyotype 47, XXY
Q981Klinefelter syndrome, male with more than two X chromosomes
Q983Other male with 46, XX karyotype
Q984Klinefelter syndrome, unspecified
Q985Karyotype 47, XYY
Q986Male with structurally abnormal sex chromosome
Q987Male with sex chromosome mosaicism
Q988Other specified sex chromosome abnormalities, male phenotype
Q989Sex chromosome abnormality, male phenotype, unspecified
Q990Chimera 46, XX/46, XY
Q99146, XX true hermaphrodite
Q998Other specified chromosome abnormalities
Q999Chromosomal abnormality, unspecified
 
PDX Collection 6777
G3289Other specified degenerative disorders of nervous system in diseases classified elsewhere
G40001Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, not intractable, with status epilepticus
G40009Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, not intractable, without status epilepticus
G40011Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, intractable, with status epilepticus
G40019Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, intractable, without status epilepticus
G40101Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, not intractable, with status epilepticus
G40109Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, not intractable, without status epilepticus
G40111Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, intractable, with status epilepticus
G40119Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, intractable, without status epilepticus
G40201Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, not intractable, with status epilepticus
G40209Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, not intractable, without status epilepticus
G40211Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, intractable, with status epilepticus
G40219Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, intractable, without status epilepticus
G40301Generalized idiopathic epilepsy and epileptic syndromes, not intractable, with status epilepticus
G40309Generalized idiopathic epilepsy and epileptic syndromes, not intractable, without status epilepticus
G40311Generalized idiopathic epilepsy and epileptic syndromes, intractable, with status epilepticus
G40319Generalized idiopathic epilepsy and epileptic syndromes, intractable, without status epilepticus
G40401Other generalized epilepsy and epileptic syndromes, not intractable, with status epilepticus
G40409Other generalized epilepsy and epileptic syndromes, not intractable, without status epilepticus
G40411Other generalized epilepsy and epileptic syndromes, intractable, with status epilepticus
G40419Other generalized epilepsy and epileptic syndromes, intractable, without status epilepticus
G4042Cyclin-Dependent Kinase-Like 5 Deficiency Disorder
G40501Epileptic seizures related to external causes, not intractable, with status epilepticus
G40509Epileptic seizures related to external causes, not intractable, without status epilepticus
G40801Other epilepsy, not intractable, with status epilepticus
G40802Other epilepsy, not intractable, without status epilepticus
G40803Other epilepsy, intractable, with status epilepticus
G40804Other epilepsy, intractable, without status epilepticus
G40811Lennox-Gastaut syndrome, not intractable, with status epilepticus
G40812Lennox-Gastaut syndrome, not intractable, without status epilepticus
G40813Lennox-Gastaut syndrome, intractable, with status epilepticus
G40814Lennox-Gastaut syndrome, intractable, without status epilepticus
G40821Epileptic spasms, not intractable, with status epilepticus
G40822Epileptic spasms, not intractable, without status epilepticus
G40823Epileptic spasms, intractable, with status epilepticus
G40824Epileptic spasms, intractable, without status epilepticus
G40833Dravet syndrome, intractable, with status epilepticus
G40834Dravet syndrome, intractable, without status epilepticus
G4089Other seizures
G40901Epilepsy, unspecified, not intractable, with status epilepticus
G40909Epilepsy, unspecified, not intractable, without status epilepticus
G40911Epilepsy, unspecified, intractable, with status epilepticus
G40919Epilepsy, unspecified, intractable, without status epilepticus
G40A01Absence epileptic syndrome, not intractable, with status epilepticus
G40A09Absence epileptic syndrome, not intractable, without status epilepticus
G40A11Absence epileptic syndrome, intractable, with status epilepticus
G40A19Absence epileptic syndrome, intractable, without status epilepticus
G40B01Juvenile myoclonic epilepsy, not intractable, with status epilepticus
G40B09Juvenile myoclonic epilepsy, not intractable, without status epilepticus
G40B11Juvenile myoclonic epilepsy, intractable, with status epilepticus
G40B19Juvenile myoclonic epilepsy, intractable, without status epilepticus
G40C01Lafora progressive myoclonus epilepsy, not intractable, with status epilepticus
G40C09Lafora progressive myoclonus epilepsy, not intractable, without status epilepticus
G40C11Lafora progressive myoclonus epilepsy, intractable, with status epilepticus
G40C19Lafora progressive myoclonus epilepsy, intractable, without status epilepticus
G9340Encephalopathy, unspecified
G9341Metabolic encephalopathy
G9342Megaloencephalic leukoencephalopathy with subcortical cysts
G9343Leukoencephalopathy with calcifications and cysts
G9344Adult-onset leukodystrophy with axonal spheroids
G9349Other encephalopathy
G939Disorder of brain, unspecified
G969Disorder of central nervous system, unspecified
G980Neurogenic arthritis, not elsewhere classified
G988Other disorders of nervous system
G998Other specified disorders of nervous system in diseases classified elsewhere
I6783Posterior reversible encephalopathy syndrome
R561Post traumatic seizures
 
PDX Collection 6778
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
I2582Chronic total occlusion of coronary artery
I2583Coronary atherosclerosis due to lipid rich plaque
I2584Coronary atherosclerosis due to calcified coronary lesion
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 6779
Q900Trisomy 21, nonmosaicism (meiotic nondisjunction)
Q901Trisomy 21, mosaicism (mitotic nondisjunction)
Q902Trisomy 21, translocation
Q909Down syndrome, unspecified
Q910Trisomy 18, nonmosaicism (meiotic nondisjunction)
Q911Trisomy 18, mosaicism (mitotic nondisjunction)
Q912Trisomy 18, translocation
Q913Trisomy 18, unspecified
Q914Trisomy 13, nonmosaicism (meiotic nondisjunction)
Q915Trisomy 13, mosaicism (mitotic nondisjunction)
Q916Trisomy 13, translocation
Q917Trisomy 13, unspecified
Q920Whole chromosome trisomy, nonmosaicism (meiotic nondisjunction)
Q921Whole chromosome trisomy, mosaicism (mitotic nondisjunction)
Q922Partial trisomy
Q925Duplications with other complex rearrangements
Q9261Marker chromosomes in normal individual
Q9262Marker chromosomes in abnormal individual
Q927Triploidy and polyploidy
Q928Other specified trisomies and partial trisomies of autosomes
Q929Trisomy and partial trisomy of autosomes, unspecified
Q930Whole chromosome monosomy, nonmosaicism (meiotic nondisjunction)
Q931Whole chromosome monosomy, mosaicism (mitotic nondisjunction)
Q932Chromosome replaced with ring, dicentric or isochromosome
Q933Deletion of short arm of chromosome 4
Q934Deletion of short arm of chromosome 5
Q9351Angelman syndrome
Q9352Phelan-McDermid syndrome
Q9359Other deletions of part of a chromosome
Q937Deletions with other complex rearrangements
Q9381Velo-cardio-facial syndrome
Q9382Williams syndrome
Q9388Other microdeletions
Q9389Other deletions from the autosomes
Q939Deletion from autosomes, unspecified
Q950Balanced translocation and insertion in normal individual
Q951Chromosome inversion in normal individual
Q952Balanced autosomal rearrangement in abnormal individual
Q953Balanced sex/autosomal rearrangement in abnormal individual
Q955Individual with autosomal fragile site
Q958Other balanced rearrangements and structural markers
Q959Balanced rearrangement and structural marker, unspecified
Q960Karyotype 45, X
Q961Karyotype 46, X iso (Xq)
Q962Karyotype 46, X with abnormal sex chromosome, except iso (Xq)
Q963Mosaicism, 45, X/46, XX or XY
Q964Mosaicism, 45, X/other cell line(s) with abnormal sex chromosome
Q968Other variants of Turner's syndrome
Q969Turner's syndrome, unspecified
Q970Karyotype 47, XXX
Q971Female with more than three X chromosomes
Q972Mosaicism, lines with various numbers of X chromosomes
Q973Female with 46, XY karyotype
Q978Other specified sex chromosome abnormalities, female phenotype
Q979Sex chromosome abnormality, female phenotype, unspecified
Q980Klinefelter syndrome karyotype 47, XXY
Q981Klinefelter syndrome, male with more than two X chromosomes
Q983Other male with 46, XX karyotype
Q984Klinefelter syndrome, unspecified
Q985Karyotype 47, XYY
Q986Male with structurally abnormal sex chromosome
Q987Male with sex chromosome mosaicism
Q988Other specified sex chromosome abnormalities, male phenotype
Q989Sex chromosome abnormality, male phenotype, unspecified
Q990Chimera 46, XX/46, XY
Q99146, XX true hermaphrodite
Q998Other specified chromosome abnormalities
Q999Chromosomal abnormality, unspecified
 
PDX Collection 6780
Q900Trisomy 21, nonmosaicism (meiotic nondisjunction)
Q901Trisomy 21, mosaicism (mitotic nondisjunction)
Q902Trisomy 21, translocation
Q909Down syndrome, unspecified
Q910Trisomy 18, nonmosaicism (meiotic nondisjunction)
Q911Trisomy 18, mosaicism (mitotic nondisjunction)
Q912Trisomy 18, translocation
Q913Trisomy 18, unspecified
Q914Trisomy 13, nonmosaicism (meiotic nondisjunction)
Q915Trisomy 13, mosaicism (mitotic nondisjunction)
Q916Trisomy 13, translocation
Q917Trisomy 13, unspecified
Q920Whole chromosome trisomy, nonmosaicism (meiotic nondisjunction)
Q921Whole chromosome trisomy, mosaicism (mitotic nondisjunction)
Q922Partial trisomy
Q925Duplications with other complex rearrangements
Q9261Marker chromosomes in normal individual
Q9262Marker chromosomes in abnormal individual
Q927Triploidy and polyploidy
Q928Other specified trisomies and partial trisomies of autosomes
Q929Trisomy and partial trisomy of autosomes, unspecified
Q930Whole chromosome monosomy, nonmosaicism (meiotic nondisjunction)
Q931Whole chromosome monosomy, mosaicism (mitotic nondisjunction)
Q932Chromosome replaced with ring, dicentric or isochromosome
Q933Deletion of short arm of chromosome 4
Q934Deletion of short arm of chromosome 5
Q9351Angelman syndrome
Q9352Phelan-McDermid syndrome
Q9359Other deletions of part of a chromosome
Q937Deletions with other complex rearrangements
Q9381Velo-cardio-facial syndrome
Q9382Williams syndrome
Q9388Other microdeletions
Q9389Other deletions from the autosomes
Q939Deletion from autosomes, unspecified
Q950Balanced translocation and insertion in normal individual
Q951Chromosome inversion in normal individual
Q952Balanced autosomal rearrangement in abnormal individual
Q953Balanced sex/autosomal rearrangement in abnormal individual
Q955Individual with autosomal fragile site
Q958Other balanced rearrangements and structural markers
Q959Balanced rearrangement and structural marker, unspecified
Q960Karyotype 45, X
Q961Karyotype 46, X iso (Xq)
Q962Karyotype 46, X with abnormal sex chromosome, except iso (Xq)
Q963Mosaicism, 45, X/46, XX or XY
Q964Mosaicism, 45, X/other cell line(s) with abnormal sex chromosome
Q968Other variants of Turner's syndrome
Q969Turner's syndrome, unspecified
Q970Karyotype 47, XXX
Q971Female with more than three X chromosomes
Q972Mosaicism, lines with various numbers of X chromosomes
Q973Female with 46, XY karyotype
Q978Other specified sex chromosome abnormalities, female phenotype
Q979Sex chromosome abnormality, female phenotype, unspecified
Q980Klinefelter syndrome karyotype 47, XXY
Q981Klinefelter syndrome, male with more than two X chromosomes
Q983Other male with 46, XX karyotype
Q984Klinefelter syndrome, unspecified
Q985Karyotype 47, XYY
Q986Male with structurally abnormal sex chromosome
Q987Male with sex chromosome mosaicism
Q988Other specified sex chromosome abnormalities, male phenotype
Q989Sex chromosome abnormality, male phenotype, unspecified
Q990Chimera 46, XX/46, XY
Q99146, XX true hermaphrodite
Q998Other specified chromosome abnormalities
Q999Chromosomal abnormality, unspecified
 
PDX Collection 6781
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
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
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
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
I25760Atherosclerosis of bypass graft of coronary artery of transplanted heart with unstable angina
I25762Atherosclerosis of bypass graft of coronary artery of transplanted heart with refractory 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
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
I2585Chronic coronary microvascular dysfunction
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



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