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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 1158 of 1375 |
PDX Collection 6192 | |
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 6193 | |
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 6194 | |
A33 | Tetanus neonatorum |
A35 | Other tetanus |
G10 | Huntington's disease |
G110 | Congenital nonprogressive ataxia |
G1110 | Early-onset cerebellar ataxia, unspecified |
G1111 | Friedreich ataxia |
G1119 | Other early-onset cerebellar ataxia |
G112 | Late-onset cerebellar ataxia |
G114 | Hereditary spastic paraplegia |
G20A1 | Parkinson's disease without dyskinesia, without mention of fluctuations |
G20A2 | Parkinson's disease without dyskinesia, with fluctuations |
G20B1 | Parkinson's disease with dyskinesia, without mention of fluctuations |
G20B2 | Parkinson's disease with dyskinesia, with fluctuations |
G20C | Parkinsonism, unspecified |
G210 | Malignant neuroleptic syndrome |
G2111 | Neuroleptic induced parkinsonism |
G2119 | Other drug induced secondary parkinsonism |
G212 | Secondary parkinsonism due to other external agents |
G213 | Postencephalitic parkinsonism |
G214 | Vascular parkinsonism |
G218 | Other secondary parkinsonism |
G219 | Secondary parkinsonism, unspecified |
G230 | Hallervorden-Spatz disease |
G231 | Progressive supranuclear ophthalmoplegia [Steele-Richardson-Olszewski] |
G232 | Striatonigral degeneration |
G233 | Hypomyelination with atrophy of the basal ganglia and cerebellum |
G238 | Other specified degenerative diseases of basal ganglia |
G239 | Degenerative disease of basal ganglia, unspecified |
G2401 | Drug induced subacute dyskinesia |
G2402 | Drug induced acute dystonia |
G2409 | Other drug induced dystonia |
G241 | Genetic torsion dystonia |
G242 | Idiopathic nonfamilial dystonia |
G243 | Spasmodic torticollis |
G244 | Idiopathic orofacial dystonia |
G245 | Blepharospasm |
G248 | Other dystonia |
G249 | Dystonia, unspecified |
G250 | Essential tremor |
G251 | Drug-induced tremor |
G252 | Other specified forms of tremor |
G253 | Myoclonus |
G254 | Drug-induced chorea |
G255 | Other chorea |
G2561 | Drug induced tics |
G2569 | Other tics of organic origin |
G2570 | Drug induced movement disorder, unspecified |
G2571 | Drug induced akathisia |
G2579 | Other drug induced movement disorders |
G2582 | Stiff-man syndrome |
G2583 | Benign shuddering attacks |
G2589 | Other specified extrapyramidal and movement disorders |
G259 | Extrapyramidal and movement disorder, unspecified |
G26 | Extrapyramidal and movement disorders in diseases classified elsewhere |
G3281 | Cerebellar ataxia in diseases classified elsewhere |
G803 | Athetoid cerebral palsy |
G8110 | Spastic hemiplegia affecting unspecified side |
G8111 | Spastic hemiplegia affecting right dominant side |
G8112 | Spastic hemiplegia affecting left dominant side |
G8113 | Spastic hemiplegia affecting right nondominant side |
G8114 | Spastic hemiplegia affecting left nondominant side |
G890 | Central pain syndrome |
G8911 | Acute pain due to trauma |
G8912 | Acute post-thoracotomy pain |
G8918 | Other acute postprocedural pain |
G8921 | Chronic pain due to trauma |
G8922 | Chronic post-thoracotomy pain |
G8928 | Other chronic postprocedural pain |
G8929 | Other chronic pain |
G893 | Neoplasm related pain (acute) (chronic) |
G894 | Chronic pain syndrome |
G903 | Multi-system degeneration of the autonomic nervous system |
R290 | Tetany |
R29700 | NIHSS score 0 |
R29701 | NIHSS score 1 |
R29702 | NIHSS score 2 |
R29703 | NIHSS score 3 |
R29704 | NIHSS score 4 |
R29705 | NIHSS score 5 |
R29706 | NIHSS score 6 |
R29707 | NIHSS score 7 |
R29708 | NIHSS score 8 |
R29709 | NIHSS score 9 |
R29710 | NIHSS score 10 |
R29711 | NIHSS score 11 |
R29712 | NIHSS score 12 |
R29713 | NIHSS score 13 |
R29714 | NIHSS score 14 |
R29715 | NIHSS score 15 |
R29716 | NIHSS score 16 |
R29717 | NIHSS score 17 |
R29718 | NIHSS score 18 |
R29719 | NIHSS score 19 |
R29720 | NIHSS score 20 |
R29721 | NIHSS score 21 |
R29722 | NIHSS score 22 |
R29723 | NIHSS score 23 |
R29724 | NIHSS score 24 |
R29725 | NIHSS score 25 |
R29726 | NIHSS score 26 |
R29727 | NIHSS score 27 |
R29728 | NIHSS score 28 |
R29729 | NIHSS score 29 |
R29730 | NIHSS score 30 |
R29731 | NIHSS score 31 |
R29732 | NIHSS score 32 |
R29733 | NIHSS score 33 |
R29734 | NIHSS score 34 |
R29735 | NIHSS score 35 |
R29736 | NIHSS score 36 |
R29737 | NIHSS score 37 |
R29738 | NIHSS score 38 |
R29739 | NIHSS score 39 |
R29740 | NIHSS score 40 |
R29741 | NIHSS score 41 |
R29742 | NIHSS score 42 |
R410 | Disorientation, unspecified |
R411 | Anterograde amnesia |
R412 | Retrograde amnesia |
R413 | Other amnesia |
R4182 | Altered mental status, unspecified |
R419 | Unspecified symptoms and signs involving cognitive functions and awareness |
R448 | Other symptoms and signs involving general sensations and perceptions |
R449 | Unspecified symptoms and signs involving general sensations and perceptions |
R4583 | Excessive crying of child, adolescent or adult |
R4584 | Anhedonia |
R460 | Very low level of personal hygiene |
R461 | Bizarre personal appearance |
R462 | Strange and inexplicable behavior |
R463 | Overactivity |
R464 | Slowness and poor responsiveness |
R465 | Suspiciousness and marked evasiveness |
R466 | Undue concern and preoccupation with stressful events |
R467 | Verbosity and circumstantial detail obscuring reason for contact |
R4681 | Obsessive-compulsive behavior |
R4689 | Other symptoms and signs involving appearance and behavior |
R52 | Pain, unspecified |
R680 | Hypothermia, not associated with low environmental temperature |
R6811 | Excessive crying of infant (baby) |
R6812 | Fussy infant (baby) |
R6813 | Apparent life threatening event in infant (ALTE) |
R6819 | Other nonspecific symptoms peculiar to infancy |
R6881 | Early satiety |
R6882 | Decreased libido |
R6883 | Chills (without fever) |
R6889 | Other general symptoms and signs |
R69 | Illness, unspecified |
PDX Collection 6195 | |
I440 | Atrioventricular block, first degree |
I441 | Atrioventricular block, second degree |
I442 | Atrioventricular block, complete |
I4430 | Unspecified atrioventricular block |
I4439 | Other atrioventricular block |
I444 | Left anterior fascicular block |
I445 | Left posterior fascicular block |
I4460 | Unspecified fascicular block |
I4469 | Other fascicular block |
I447 | Left bundle-branch block, unspecified |
I450 | Right fascicular block |
I4510 | Unspecified right bundle-branch block |
I4519 | Other right bundle-branch block |
I452 | Bifascicular block |
I453 | Trifascicular block |
I454 | Nonspecific intraventricular block |
I455 | Other specified heart block |
I456 | Pre-excitation syndrome |
I4581 | Long QT syndrome |
I4589 | Other specified conduction disorders |
I459 | Conduction disorder, unspecified |
I462 | Cardiac arrest due to underlying cardiac condition |
I468 | Cardiac arrest due to other underlying condition |
I469 | Cardiac arrest, cause unspecified |
I470 | Re-entry ventricular arrhythmia |
I4710 | Supraventricular tachycardia, unspecified |
I4711 | Inappropriate sinus tachycardia, so stated |
I4719 | Other supraventricular tachycardia |
I4720 | Ventricular tachycardia, unspecified |
I4721 | Torsades de pointes |
I4729 | Other ventricular tachycardia |
I479 | Paroxysmal tachycardia, unspecified |
I480 | Paroxysmal atrial fibrillation |
I4811 | Longstanding persistent atrial fibrillation |
I4819 | Other persistent atrial fibrillation |
I4820 | Chronic atrial fibrillation, unspecified |
I4821 | Permanent atrial fibrillation |
I483 | Typical atrial flutter |
I484 | Atypical atrial flutter |
I4891 | Unspecified atrial fibrillation |
I4892 | Unspecified atrial flutter |
I4901 | Ventricular fibrillation |
I4902 | Ventricular flutter |
I492 | Junctional premature depolarization |
I498 | Other specified cardiac arrhythmias |
I878 | Other specified disorders of veins |
I879 | Disorder of vein, unspecified |
I998 | Other disorder of circulatory system |
I999 | Unspecified disorder of circulatory system |
R001 | Bradycardia, unspecified |
PDX Collection 6196 | |
C880 | Waldenstrom macroglobulinemia |
D472 | Monoclonal gammopathy |
D890 | Polyclonal hypergammaglobulinemia |
D891 | Cryoglobulinemia |
E700 | Classical phenylketonuria |
E701 | Other hyperphenylalaninemias |
E7020 | Disorder of tyrosine metabolism, unspecified |
E7021 | Tyrosinemia |
E7029 | Other disorders of tyrosine metabolism |
E7030 | Albinism, unspecified |
E70310 | X-linked ocular albinism |
E70311 | Autosomal recessive ocular albinism |
E70318 | Other ocular albinism |
E70319 | Ocular albinism, unspecified |
E70320 | Tyrosinase negative oculocutaneous albinism |
E70321 | Tyrosinase positive oculocutaneous albinism |
E70328 | Other oculocutaneous albinism |
E70329 | Oculocutaneous albinism, unspecified |
E70330 | Chediak-Higashi syndrome |
E70331 | Hermansky-Pudlak syndrome |
E70338 | Other albinism with hematologic abnormality |
E70339 | Albinism with hematologic abnormality, unspecified |
E7039 | Other specified albinism |
E7040 | Disorders of histidine metabolism, unspecified |
Centers for Medicare & Medicaid Services, 7500 Security Boulevard Baltimore, MD 21244 01 Mar 2023 06:12:40 CMS, code-revision=344, description-revision=1357 |