ICD-10-CM/PCS MS-DRG v41.0 Definitions Manual
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DRAFT
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 1156 of 1375 |
| PDX Collection 6181 (continued) | |
| Q2121 | Partial atrioventricular septal defect |
| Q2122 | Transitional atrioventricular septal defect |
| Q2123 | Complete atrioventricular septal defect |
| Q213 | Tetralogy of Fallot |
| Q214 | Aortopulmonary septal defect |
| Q218 | Other congenital malformations of cardiac septa |
| Q219 | Congenital malformation of cardiac septum, unspecified |
| Q238 | Other congenital malformations of aortic and mitral valves |
| Q239 | Congenital malformation of aortic and mitral valves, unspecified |
| Q248 | Other specified congenital malformations of heart |
| Q249 | Congenital malformation of heart, unspecified |
| Q2730 | Arteriovenous malformation, site unspecified |
| Q274 | Congenital phlebectasia |
| Q280 | Arteriovenous malformation of precerebral vessels |
| Q281 | Other malformations of precerebral vessels |
| Q288 | Other specified congenital malformations of circulatory system |
| Q289 | Congenital malformation of circulatory system, unspecified |
| Q8711 | Prader-Willi syndrome |
| Q8719 | Other congenital malformation syndromes predominantly associated with short stature |
| Q872 | Congenital malformation syndromes predominantly involving limbs |
| Q873 | Congenital malformation syndromes involving early overgrowth |
| Q8740 | Marfan syndrome, unspecified |
| Q87410 | Marfan syndrome with aortic dilation |
| Q87418 | Marfan syndrome with other cardiovascular manifestations |
| Q8742 | Marfan syndrome with ocular manifestations |
| Q8743 | Marfan syndrome with skeletal manifestation |
| Q875 | Other congenital malformation syndromes with other skeletal changes |
| Q8781 | Alport syndrome |
| Q8782 | Arterial tortuosity syndrome |
| Q8783 | Bardet-Biedl syndrome |
| Q8784 | Laurence-Moon syndrome |
| Q8785 | MED13L syndrome |
| Q8789 | Other specified congenital malformation syndromes, not elsewhere classified |
| Q897 | Multiple congenital malformations, not elsewhere classified |
| Q898 | Other specified congenital malformations |
| Q992 | Fragile X chromosome |
| PDX Collection 6182 | |
| E7871 | Barth syndrome |
| E7872 | Smith-Lemli-Opitz syndrome |
| I230 | Hemopericardium as current complication following acute myocardial infarction |
| I231 | Atrial septal defect as current complication following acute myocardial infarction |
| I232 | Ventricular septal defect as current complication following acute myocardial infarction |
| I233 | Rupture of cardiac wall without hemopericardium as current complication following acute myocardial infarction |
| I234 | Rupture of chordae tendineae as current complication following acute myocardial infarction |
| I235 | Rupture of papillary muscle as current complication following acute myocardial infarction |
| I236 | Thrombosis of atrium, auricular appendage, and ventricle as current complications following acute myocardial infarction |
| I237 | Postinfarction angina |
| I238 | Other current complications following acute myocardial infarction |
| I400 | Infective myocarditis |
| I401 | Isolated myocarditis |
| I408 | Other acute myocarditis |
| I409 | Acute myocarditis, unspecified |
| I41 | Myocarditis in diseases classified elsewhere |
| I510 | Cardiac septal defect, acquired |
| I511 | Rupture of chordae tendineae, not elsewhere classified |
| I512 | Rupture of papillary muscle, not elsewhere classified |
| I514 | Myocarditis, unspecified |
| I878 | Other specified disorders of veins |
| I879 | Disorder of vein, unspecified |
| I970 | Postcardiotomy syndrome |
| I97110 | Postprocedural cardiac insufficiency following cardiac surgery |
| I97111 | Postprocedural cardiac insufficiency following other surgery |
| I97120 | Postprocedural cardiac arrest following cardiac surgery |
| I97121 | Postprocedural cardiac arrest following other surgery |
| I97130 | Postprocedural heart failure following cardiac surgery |
| I97131 | Postprocedural heart failure following other surgery |
| I97190 | Other postprocedural cardiac functional disturbances following cardiac surgery |
| I97191 | Other postprocedural cardiac functional disturbances following other surgery |
| I998 | Other disorder of circulatory system |
| I999 | Unspecified disorder of circulatory system |
| P2930 | Pulmonary hypertension of newborn |
| P2938 | Other persistent fetal circulation |
| Q200 | Common arterial trunk |
| Q201 | Double outlet right ventricle |
| Q202 | Double outlet left ventricle |
| Q203 | Discordant ventriculoarterial connection |
| Q204 | Double inlet ventricle |
| Q205 | Discordant atrioventricular connection |
| Q206 | Isomerism of atrial appendages |
| Q208 | Other congenital malformations of cardiac chambers and connections |
| Q209 | Congenital malformation of cardiac chambers and connections, unspecified |
| Q210 | Ventricular septal defect |
| Q2110 | Atrial septal defect, unspecified |
| Q2111 | Secundum atrial septal defect |
| Q2112 | Patent foramen ovale |
| Q2113 | Coronary sinus atrial septal defect |
| Q2114 | Superior sinus venosus atrial septal defect |
| Q2115 | Inferior sinus venosus atrial septal defect |
| Q2116 | Sinus venosus atrial septal defect, unspecified |
| Q2119 | Other specified atrial septal defect |
| Q2120 | Atrioventricular septal defect, unspecified as to partial or complete |
| Q2121 | Partial atrioventricular septal defect |
| Q2122 | Transitional atrioventricular septal defect |
| Q2123 | Complete atrioventricular septal defect |
| Q213 | Tetralogy of Fallot |
| Q214 | Aortopulmonary septal defect |
| Q218 | Other congenital malformations of cardiac septa |
| Q219 | Congenital malformation of cardiac septum, unspecified |
| Q238 | Other congenital malformations of aortic and mitral valves |
| Q239 | Congenital malformation of aortic and mitral valves, unspecified |
| Q248 | Other specified congenital malformations of heart |
| Q249 | Congenital malformation of heart, unspecified |
| Q2730 | Arteriovenous malformation, site unspecified |
| Q274 | Congenital phlebectasia |
| Q280 | Arteriovenous malformation of precerebral vessels |
| Q281 | Other malformations of precerebral vessels |
| Q288 | Other specified congenital malformations of circulatory system |
| Q289 | Congenital malformation of circulatory system, unspecified |
| Q8711 | Prader-Willi syndrome |
| Q8719 | Other congenital malformation syndromes predominantly associated with short stature |
| Q872 | Congenital malformation syndromes predominantly involving limbs |
| Q873 | Congenital malformation syndromes involving early overgrowth |
| Q8740 | Marfan syndrome, unspecified |
| Q87410 | Marfan syndrome with aortic dilation |
| Q87418 | Marfan syndrome with other cardiovascular manifestations |
| Q8742 | Marfan syndrome with ocular manifestations |
| Q8743 | Marfan syndrome with skeletal manifestation |
| Q875 | Other congenital malformation syndromes with other skeletal changes |
| Q8781 | Alport syndrome |
| Q8782 | Arterial tortuosity syndrome |
| Q8783 | Bardet-Biedl syndrome |
| Q8784 | Laurence-Moon syndrome |
| Q8785 | MED13L syndrome |
| Q8789 | Other specified congenital malformation syndromes, not elsewhere classified |
| Q897 | Multiple congenital malformations, not elsewhere classified |
| Q898 | Other specified congenital malformations |
| Q992 | Fragile X chromosome |
| PDX Collection 6183 | |
| K634 | Enteroptosis |
| K638211 | Small intestinal bacterial overgrowth, hydrogen-subtype |
| K638212 | Small intestinal bacterial overgrowth, hydrogen sulfide-subtype |
| K638219 | Small intestinal bacterial overgrowth, unspecified |
| K63822 | Small intestinal fungal overgrowth |
| K63829 | Intestinal methanogen overgrowth, unspecified |
| K6389 | Other specified diseases of intestine |
| K639 | Disease of intestine, unspecified |
| K650 | Generalized (acute) peritonitis |
| K651 | Peritoneal abscess |
| K652 | Spontaneous bacterial peritonitis |
| K653 | Choleperitonitis |
| K654 | Sclerosing mesenteritis |
| K658 | Other peritonitis |
| K659 | Peritonitis, unspecified |
| K67 | Disorders of peritoneum in infectious diseases classified elsewhere |
| K6819 | Other retroperitoneal abscess |
| K682 | Retroperitoneal fibrosis |
| K683 | Retroperitoneal hematoma |
| K689 | Other disorders of retroperitoneum |
| K9289 | Other specified diseases of the digestive system |
| K929 | Disease of digestive system, unspecified |
| R1113 | Vomiting of fecal matter |
| PDX Collection 6184 | |
| E7871 | Barth syndrome |
| E7872 | Smith-Lemli-Opitz syndrome |
| I230 | Hemopericardium as current complication following acute myocardial infarction |
| I231 | Atrial septal defect as current complication following acute myocardial infarction |
| I232 | Ventricular septal defect as current complication following acute myocardial infarction |
| I233 | Rupture of cardiac wall without hemopericardium as current complication following acute myocardial infarction |
| I234 | Rupture of chordae tendineae as current complication following acute myocardial infarction |
| I235 | Rupture of papillary muscle as current complication following acute myocardial infarction |
| I236 | Thrombosis of atrium, auricular appendage, and ventricle as current complications following acute myocardial infarction |
| I237 | Postinfarction angina |
| I238 | Other current complications following acute myocardial infarction |
| I400 | Infective myocarditis |
| I401 | Isolated myocarditis |
| I408 | Other acute myocarditis |
| I409 | Acute myocarditis, unspecified |
| I41 | Myocarditis in diseases classified elsewhere |
| I510 | Cardiac septal defect, acquired |
| I511 | Rupture of chordae tendineae, not elsewhere classified |
| I512 | Rupture of papillary muscle, not elsewhere classified |
| I514 | Myocarditis, unspecified |
| I878 | Other specified disorders of veins |
| I879 | Disorder of vein, unspecified |
| I970 | Postcardiotomy syndrome |
| I97110 | Postprocedural cardiac insufficiency following cardiac surgery |
| I97111 | Postprocedural cardiac insufficiency following other surgery |
| I97120 | Postprocedural cardiac arrest following cardiac surgery |
| I97121 | Postprocedural cardiac arrest following other surgery |
| I97130 | Postprocedural heart failure following cardiac surgery |
| I97131 | Postprocedural heart failure following other surgery |
| I97190 | Other postprocedural cardiac functional disturbances following cardiac surgery |
| I97191 | Other postprocedural cardiac functional disturbances following other surgery |
| I998 | Other disorder of circulatory system |
| I999 | Unspecified disorder of circulatory system |
| P2930 | Pulmonary hypertension of newborn |
| P2938 | Other persistent fetal circulation |
| Q200 | Common arterial trunk |
| Q201 | Double outlet right ventricle |
| Q202 | Double outlet left ventricle |
| Q203 | Discordant ventriculoarterial connection |
| Q204 | Double inlet ventricle |
| Q205 | Discordant atrioventricular connection |
| Q206 | Isomerism of atrial appendages |
| Q208 | Other congenital malformations of cardiac chambers and connections |
| Q209 | Congenital malformation of cardiac chambers and connections, unspecified |
| Q210 | Ventricular septal defect |
| Q2110 | Atrial septal defect, unspecified |
| Q2111 | Secundum atrial septal defect |
| Q2112 | Patent foramen ovale |
| Q2113 | Coronary sinus atrial septal defect |
| Q2114 | Superior sinus venosus atrial septal defect |
| Q2115 | Inferior sinus venosus atrial septal defect |
| Q2116 | Sinus venosus atrial septal defect, unspecified |
| Q2119 | Other specified atrial septal defect |
| Q2120 | Atrioventricular septal defect, unspecified as to partial or complete |
| Q2121 | Partial atrioventricular septal defect |
| Q2122 | Transitional atrioventricular septal defect |
| Q2123 | Complete atrioventricular septal defect |
| Q213 | Tetralogy of Fallot |
| Q214 | Aortopulmonary septal defect |
| Q218 | Other congenital malformations of cardiac septa |
| Q219 | Congenital malformation of cardiac septum, unspecified |
| Q238 | Other congenital malformations of aortic and mitral valves |
| Q239 | Congenital malformation of aortic and mitral valves, unspecified |
| Q248 | Other specified congenital malformations of heart |
| Q249 | Congenital malformation of heart, unspecified |
| Q2730 | Arteriovenous malformation, site unspecified |
| Q274 | Congenital phlebectasia |
| Q280 | Arteriovenous malformation of precerebral vessels |
| Q281 | Other malformations of precerebral vessels |
| Q288 | Other specified congenital malformations of circulatory system |
| Q289 | Congenital malformation of circulatory system, unspecified |
| Q8711 | Prader-Willi syndrome |
| Q8719 | Other congenital malformation syndromes predominantly associated with short stature |
| Q872 | Congenital malformation syndromes predominantly involving limbs |
| Q873 | Congenital malformation syndromes involving early overgrowth |
| Q8740 | Marfan syndrome, unspecified |
| Q87410 | Marfan syndrome with aortic dilation |
| Q87418 | Marfan syndrome with other cardiovascular manifestations |
| Q8742 | Marfan syndrome with ocular manifestations |
| Q8743 | Marfan syndrome with skeletal manifestation |
| Q875 | Other congenital malformation syndromes with other skeletal changes |
| Q8781 | Alport syndrome |
| Q8782 | Arterial tortuosity syndrome |
| Q8783 | Bardet-Biedl syndrome |
| Q8784 | Laurence-Moon syndrome |
| Q8785 | MED13L syndrome |
| Q8789 | Other specified congenital malformation syndromes, not elsewhere classified |
| Q897 | Multiple congenital malformations, not elsewhere classified |
| Q898 | Other specified congenital malformations |
| Q992 | Fragile X chromosome |
| PDX Collection 6185 | |
| E7871 | Barth syndrome |
| E7872 | Smith-Lemli-Opitz syndrome |
| I230 | Hemopericardium as current complication following acute myocardial infarction |
| I231 | Atrial septal defect as current complication following acute myocardial infarction |
| I232 | Ventricular septal defect as current complication following acute myocardial infarction |
| I233 | Rupture of cardiac wall without hemopericardium as current complication following acute myocardial infarction |
| I234 | Rupture of chordae tendineae as current complication following acute myocardial infarction |
| I235 | Rupture of papillary muscle as current complication following acute myocardial infarction |
| I236 | Thrombosis of atrium, auricular appendage, and ventricle as current complications following acute myocardial infarction |
| I237 | Postinfarction angina |
| I238 | Other current complications following acute myocardial infarction |
| I400 | Infective myocarditis |
| I401 | Isolated myocarditis |
| I408 | Other acute myocarditis |
| I409 | Acute myocarditis, unspecified |
| I41 | Myocarditis in diseases classified elsewhere |
| I510 | Cardiac septal defect, acquired |
| I511 | Rupture of chordae tendineae, not elsewhere classified |
| I512 | Rupture of papillary muscle, not elsewhere classified |
| I514 | Myocarditis, unspecified |
| I878 | Other specified disorders of veins |
| I879 | Disorder of vein, unspecified |
| I970 | Postcardiotomy syndrome |
| I97110 | Postprocedural cardiac insufficiency following cardiac surgery |
| I97111 | Postprocedural cardiac insufficiency following other surgery |
| I97120 | Postprocedural cardiac arrest following cardiac surgery |
| I97121 | Postprocedural cardiac arrest following other surgery |
| I97130 | Postprocedural heart failure following cardiac surgery |
| I97131 | Postprocedural heart failure following other surgery |
| I97190 | Other postprocedural cardiac functional disturbances following cardiac surgery |
| I97191 | Other postprocedural cardiac functional disturbances following other surgery |
| I998 | Other disorder of circulatory system |
| I999 | Unspecified disorder of circulatory system |
| P2930 | Pulmonary hypertension of newborn |
| P2938 | Other persistent fetal circulation |
| Q200 | Common arterial trunk |
| Q201 | Double outlet right ventricle |
| Q202 | Double outlet left ventricle |
| Q203 | Discordant ventriculoarterial connection |
| Q204 | Double inlet ventricle |
| Q205 | Discordant atrioventricular connection |
| Q206 | Isomerism of atrial appendages |
| Q208 | Other congenital malformations of cardiac chambers and connections |
| Q209 | Congenital malformation of cardiac chambers and connections, unspecified |
| Q210 | Ventricular septal defect |
| Q2110 | Atrial septal defect, unspecified |
| Q2111 | Secundum atrial septal defect |
| Q2112 | Patent foramen ovale |
| Q2113 | Coronary sinus atrial septal defect |
| Q2114 | Superior sinus venosus atrial septal defect |
| Q2115 | Inferior sinus venosus atrial septal defect |
| Q2116 | Sinus venosus atrial septal defect, unspecified |
| Q2119 | Other specified atrial septal defect |
| Q2120 | Atrioventricular septal defect, unspecified as to partial or complete |
| Q2121 | Partial atrioventricular septal defect |
| Q2122 | Transitional atrioventricular septal defect |
| Q2123 | Complete atrioventricular septal defect |
| Q213 | Tetralogy of Fallot |
| Q214 | Aortopulmonary septal defect |
| Q218 | Other congenital malformations of cardiac septa |
| Q219 | Congenital malformation of cardiac septum, unspecified |
| Q238 | Other congenital malformations of aortic and mitral valves |
| Q239 | Congenital malformation of aortic and mitral valves, unspecified |
| Q248 | Other specified congenital malformations of heart |
| Q249 | Congenital malformation of heart, unspecified |
| Q2730 | Arteriovenous malformation, site unspecified |
| Q274 | Congenital phlebectasia |
| Q280 | Arteriovenous malformation of precerebral vessels |
| Q281 | Other malformations of precerebral vessels |
| Q288 | Other specified congenital malformations of circulatory system |
| Q289 | Congenital malformation of circulatory system, unspecified |
| Q8711 | Prader-Willi syndrome |
| Q8719 | Other congenital malformation syndromes predominantly associated with short stature |
| Q872 | Congenital malformation syndromes predominantly involving limbs |
| Q873 | Congenital malformation syndromes involving early overgrowth |
| Q8740 | Marfan syndrome, unspecified |
| Q87410 | Marfan syndrome with aortic dilation |
| Q87418 | Marfan syndrome with other cardiovascular manifestations |
| Q8742 | Marfan syndrome with ocular manifestations |
| Q8743 | Marfan syndrome with skeletal manifestation |
| Q875 | Other congenital malformation syndromes with other skeletal changes |
| Q8781 | Alport syndrome |
| Q8782 | Arterial tortuosity syndrome |
| Q8783 | Bardet-Biedl syndrome |
| Q8784 | Laurence-Moon syndrome |
| Q8785 | MED13L syndrome |
| Q8789 | Other specified congenital malformation syndromes, not elsewhere classified |
| Q897 | Multiple congenital malformations, not elsewhere classified |
| Q898 | Other specified congenital malformations |
| Q992 | Fragile X chromosome |
| PDX Collection 6186 | |
| K634 | Enteroptosis |
| K638211 | Small intestinal bacterial overgrowth, hydrogen-subtype |
| K638212 | Small intestinal bacterial overgrowth, hydrogen sulfide-subtype |
| K638219 | Small intestinal bacterial overgrowth, unspecified |
| K63822 | Small intestinal fungal overgrowth |
| K63829 | Intestinal methanogen overgrowth, unspecified |
| K6389 | Other specified diseases of intestine |
| K639 | Disease of intestine, unspecified |
| K650 | Generalized (acute) peritonitis |
| K651 | Peritoneal abscess |
| K652 | Spontaneous bacterial peritonitis |
| K653 | Choleperitonitis |
| K654 | Sclerosing mesenteritis |
| K658 | Other peritonitis |
| K659 | Peritonitis, unspecified |
| K67 | Disorders of peritoneum in infectious diseases classified elsewhere |
| K6819 | Other retroperitoneal abscess |
| K682 | Retroperitoneal fibrosis |
| K683 | Retroperitoneal hematoma |
| K689 | Other disorders of retroperitoneum |
| K9289 | Other specified diseases of the digestive system |
| K929 | Disease of digestive system, unspecified |
| R1113 | Vomiting of fecal matter |
| PDX Collection 6187 | |
| K634 | Enteroptosis |
| K638211 | Small intestinal bacterial overgrowth, hydrogen-subtype |
| K638212 | Small intestinal bacterial overgrowth, hydrogen sulfide-subtype |
| K638219 | Small intestinal bacterial overgrowth, unspecified |
| K63822 | Small intestinal fungal overgrowth |
| K63829 | Intestinal methanogen overgrowth, unspecified |
| K6389 | Other specified diseases of intestine |
| K639 | Disease of intestine, unspecified |
| K650 | Generalized (acute) peritonitis |
| K651 | Peritoneal abscess |
| K652 | Spontaneous bacterial peritonitis |
| K653 | Choleperitonitis |
| K654 | Sclerosing mesenteritis |
| K658 | Other peritonitis |
| K659 | Peritonitis, unspecified |
| K67 | Disorders of peritoneum in infectious diseases classified elsewhere |
| K6819 | Other retroperitoneal abscess |
| K682 | Retroperitoneal fibrosis |
| K683 | Retroperitoneal hematoma |
| K689 | Other disorders of retroperitoneum |
| K9289 | Other specified diseases of the digestive system |
| K929 | Disease of digestive system, unspecified |
| R1113 | Vomiting of fecal matter |
| PDX Collection 6188 | |
| A179 | Tuberculosis of nervous system, unspecified |
| A1810 | Tuberculosis of genitourinary system, unspecified |
| A1811 | Tuberculosis of kidney and ureter |
| A1813 | Tuberculosis of other urinary organs |
| A1882 | Tuberculosis of other endocrine glands |
| A1884 | Tuberculosis of heart |
| A1889 | Tuberculosis of other sites |
| A5421 | Gonococcal infection of kidney and ureter |
| A5429 | Other gonococcal genitourinary infections |
| A5482 | Gonococcal brain abscess |
| A5484 | Gonococcal pneumonia |
| A5489 | Other gonococcal infections |
| A549 | Gonococcal infection, unspecified |
| A5900 | Urogenital trichomoniasis, unspecified |
| A598 | Trichomoniasis of other sites |
| A599 | Trichomoniasis, unspecified |
| A985 | Hemorrhagic fever with renal syndrome |
| B3741 | Candidal cystitis and urethritis |
| B3742 | Candidal balanitis |
| B3749 | Other urogenital candidiasis |
| B9721 | SARS-associated coronavirus as the cause of diseases classified elsewhere |
| E0821 | Diabetes mellitus due to underlying condition with diabetic nephropathy |
| E0822 | Diabetes mellitus due to underlying condition with diabetic chronic kidney disease |
| E0829 | Diabetes mellitus due to underlying condition with other diabetic kidney complication |
| E08618 | Diabetes mellitus due to underlying condition with other diabetic arthropathy |
| E08620 | Diabetes mellitus due to underlying condition with diabetic dermatitis |
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Centers for Medicare & Medicaid Services, 7500 Security Boulevard Baltimore, MD 21244 01 Mar 2023 06:12:40 CMS, code-revision=344, description-revision=1357 |