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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 1248 of 1375 |
PDX Collection 6580 (continued) | |
E7410 | Disorder of fructose metabolism, unspecified |
E7411 | Essential fructosuria |
E7412 | Hereditary fructose intolerance |
E7419 | Other disorders of fructose metabolism |
E7420 | Disorders of galactose metabolism, unspecified |
E7421 | Galactosemia |
E7429 | Other disorders of galactose metabolism |
E7431 | Sucrase-isomaltase deficiency |
E7439 | Other disorders of intestinal carbohydrate absorption |
E744 | Disorders of pyruvate metabolism and gluconeogenesis |
E74810 | Glucose transporter protein type 1 deficiency |
E74818 | Other disorders of glucose transport |
E74819 | Disorders of glucose transport, unspecified |
E7489 | Other specified disorders of carbohydrate metabolism |
E749 | Disorder of carbohydrate metabolism, unspecified |
E7521 | Fabry (-Anderson) disease |
E7522 | Gaucher disease |
E75240 | Niemann-Pick disease type A |
E75241 | Niemann-Pick disease type B |
E75242 | Niemann-Pick disease type C |
E75243 | Niemann-Pick disease type D |
E75248 | Other Niemann-Pick disease |
E75249 | Niemann-Pick disease, unspecified |
E753 | Sphingolipidosis, unspecified |
E755 | Other lipid storage disorders |
E756 | Lipid storage disorder, unspecified |
E770 | Defects in post-translational modification of lysosomal enzymes |
E771 | Defects in glycoprotein degradation |
E778 | Other disorders of glycoprotein metabolism |
E779 | Disorder of glycoprotein metabolism, unspecified |
E7800 | Pure hypercholesterolemia, unspecified |
E7801 | Familial hypercholesterolemia |
E781 | Pure hyperglyceridemia |
E782 | Mixed hyperlipidemia |
E783 | Hyperchylomicronemia |
E7841 | Elevated Lipoprotein(a) |
E7849 | Other hyperlipidemia |
E785 | Hyperlipidemia, unspecified |
E786 | Lipoprotein deficiency |
E7870 | Disorder of bile acid and cholesterol metabolism, unspecified |
E7879 | Other disorders of bile acid and cholesterol metabolism |
E7881 | Lipoid dermatoarthritis |
E7889 | Other lipoprotein metabolism disorders |
E789 | Disorder of lipoprotein metabolism, unspecified |
E8802 | Plasminogen deficiency |
E8809 | Other disorders of plasma-protein metabolism, not elsewhere classified |
E881 | Lipodystrophy, not elsewhere classified |
E882 | Lipomatosis, not elsewhere classified |
E88811 | Insulin resistance syndrome, Type A |
E88818 | Other insulin resistance |
E88819 | Insulin resistance, unspecified |
E8889 | Other specified metabolic disorders |
PDX Collection 6581 | |
E7871 | Barth syndrome |
E7872 | Smith-Lemli-Opitz syndrome |
P2930 | Pulmonary hypertension of newborn |
P2938 | Other persistent fetal circulation |
Q209 | Congenital malformation of cardiac chambers and connections, unspecified |
Q224 | Congenital tricuspid stenosis |
Q225 | Ebstein's anomaly |
Q226 | Hypoplastic right heart syndrome |
Q228 | Other congenital malformations of tricuspid valve |
Q229 | Congenital malformation of tricuspid valve, unspecified |
Q230 | Congenital stenosis of aortic valve |
Q231 | Congenital insufficiency of aortic valve |
Q232 | Congenital mitral stenosis |
Q233 | Congenital mitral insufficiency |
Q234 | Hypoplastic left heart syndrome |
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 6582 | |
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 6583 | |
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 |
R0989 | Other specified symptoms and signs involving the circulatory and respiratory systems |
R09A0 | Foreign body sensation, unspecified |
R09A1 | Foreign body sensation, nose |
R09A2 | Foreign body sensation, throat |
R09A9 | Foreign body sensation, other site |
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 |
R570 | Cardiogenic shock |
R571 | Hypovolemic shock |
R578 | Other shock |
R579 | Shock, unspecified |
R6521 | Severe sepsis with septic shock |
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 6584 | |
A150 | Tuberculosis of lung |
A154 | Tuberculosis of intrathoracic lymph nodes |
A155 | Tuberculosis of larynx, trachea and bronchus |
A156 | Tuberculous pleurisy |
A158 | Other respiratory tuberculosis |
A159 | Respiratory tuberculosis unspecified |
A179 | Tuberculosis of nervous system, unspecified |
A1882 | Tuberculosis of other endocrine glands |
A1884 | Tuberculosis of heart |
A1889 | Tuberculosis of other sites |
J22 | Unspecified acute lower respiratory infection |
J4481 | Bronchiolitis obliterans and bronchiolitis obliterans syndrome |
J4489 | Other specified chronic obstructive pulmonary disease |
J449 | Chronic obstructive pulmonary disease, unspecified |
J470 | Bronchiectasis with acute lower respiratory infection |
J471 | Bronchiectasis with (acute) exacerbation |
J479 | Bronchiectasis, uncomplicated |
J4A0 | Restrictive allograft syndrome |
J4A8 | Other chronic lung allograft dysfunction |
J4A9 | Chronic lung allograft dysfunction, unspecified |
J60 | Coalworker's pneumoconiosis |
J61 | Pneumoconiosis due to asbestos and other mineral fibers |
J620 | Pneumoconiosis due to talc dust |
J628 | Pneumoconiosis due to other dust containing silica |
J630 | Aluminosis (of lung) |
J631 | Bauxite fibrosis (of lung) |
J632 | Berylliosis |
J633 | Graphite fibrosis (of lung) |
J634 | Siderosis |
J635 | Stannosis |
J636 | Pneumoconiosis due to other specified inorganic dusts |
J64 | Unspecified pneumoconiosis |
J65 | Pneumoconiosis associated with tuberculosis |
J660 | Byssinosis |
J661 | Flax-dressers' disease |
J662 | Cannabinosis |
J668 | Airway disease due to other specific organic dusts |
J670 | Farmer's lung |
J671 | Bagassosis |
J672 | Bird fancier's lung |
J673 | Suberosis |
J674 | Maltworker's lung |
J675 | Mushroom-worker's lung |
J676 | Maple-bark-stripper's lung |
J677 | Air conditioner and humidifier lung |
J678 | Hypersensitivity pneumonitis due to other organic dusts |
J679 | Hypersensitivity pneumonitis due to unspecified organic dust |
J680 | Bronchitis and pneumonitis due to chemicals, gases, fumes and vapors |
J681 | Pulmonary edema due to chemicals, gases, fumes and vapors |
J682 | Upper respiratory inflammation due to chemicals, gases, fumes and vapors, not elsewhere classified |
J683 | Other acute and subacute respiratory conditions due to chemicals, gases, fumes and vapors |
J684 | Chronic respiratory conditions due to chemicals, gases, fumes and vapors |
J688 | Other respiratory conditions due to chemicals, gases, fumes and vapors |
J689 | Unspecified respiratory condition due to chemicals, gases, fumes and vapors |
J690 | Pneumonitis due to inhalation of food and vomit |
J691 | Pneumonitis due to inhalation of oils and essences |
J698 | Pneumonitis due to inhalation of other solids and liquids |
J700 | Acute pulmonary manifestations due to radiation |
J701 | Chronic and other pulmonary manifestations due to radiation |
J702 | Acute drug-induced interstitial lung disorders |
J703 | Chronic drug-induced interstitial lung disorders |
J704 | Drug-induced interstitial lung disorders, unspecified |
J708 | Respiratory conditions due to other specified external agents |
J709 | Respiratory conditions due to unspecified external agent |
J8401 | Alveolar proteinosis |
J8402 | Pulmonary alveolar microlithiasis |
J8403 | Idiopathic pulmonary hemosiderosis |
J8409 | Other alveolar and parieto-alveolar conditions |
J8410 | Pulmonary fibrosis, unspecified |
J84111 | Idiopathic interstitial pneumonia, not otherwise specified |
J84112 | Idiopathic pulmonary fibrosis |
J84113 | Idiopathic non-specific interstitial pneumonitis |
J84114 | Acute interstitial pneumonitis |
J84115 | Respiratory bronchiolitis interstitial lung disease |
J84116 | Cryptogenic organizing pneumonia |
J84117 | Desquamative interstitial pneumonia |
J84170 | Interstitial lung disease with progressive fibrotic phenotype in diseases classified elsewhere |
J84178 | Other interstitial pulmonary diseases with fibrosis in diseases classified elsewhere |
J842 | Lymphoid interstitial pneumonia |
J8481 | Lymphangioleiomyomatosis |
J8482 | Adult pulmonary Langerhans cell histiocytosis |
J8489 | Other specified interstitial pulmonary diseases |
J849 | Interstitial pulmonary disease, unspecified |
J984 | Other disorders of lung |
J988 | Other specified respiratory disorders |
J989 | Respiratory disorder, unspecified |
J99 | Respiratory disorders in diseases classified elsewhere |
N80B1 | Endometriosis of pleura |
N80B2 | Endometriosis of lung |
N80B31 | Superficial endometriosis of diaphragm |
N80B32 | Deep endometriosis of diaphragm |
N80B39 | Endometriosis of diaphragm, unspecified depth |
Q334 | Congenital bronchiectasis |
R911 | Solitary pulmonary nodule |
PDX Collection 6585 | |
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 |
E7041 | Histidinemia |
E7049 | Other disorders of histidine metabolism |
E705 | Disorders of tryptophan metabolism |
Centers for Medicare & Medicaid Services, 7500 Security Boulevard Baltimore, MD 21244 01 Mar 2023 06:12:40 CMS, code-revision=344, description-revision=1357 |