DRAFT
ICD-10-CM/PCS MS-DRG v40.0 Definitions Manual |
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Appendix C: Principal diagnoses which convert CC/MCC to non-CC |
Page 288 of 1270 |
PDX Collection 3486 | |
Z1622 | Resistance to vancomycin related antibiotics |
PDX Collection 3487 | |
Z1623 | Resistance to quinolones and fluoroquinolones |
PDX Collection 3488 | |
Z1629 | Resistance to other single specified antibiotic |
PDX Collection 3489 | |
Z1630 | Resistance to unspecified antimicrobial drugs |
PDX Collection 3490 | |
Z1631 | Resistance to antiparasitic drug(s) |
PDX Collection 3491 | |
Z1632 | Resistance to antifungal drug(s) |
PDX Collection 3492 | |
Z1633 | Resistance to antiviral drug(s) |
PDX Collection 3493 | |
Z16341 | Resistance to single antimycobacterial drug |
PDX Collection 3494 | |
Z16342 | Resistance to multiple antimycobacterial drugs |
PDX Collection 3495 | |
Z1635 | Resistance to multiple antimicrobial drugs |
PDX Collection 3496 | |
Z1610 | Resistance to unspecified beta lactam antibiotics |
PDX Collection 3497 | |
Z1611 | Resistance to penicillins |
PDX Collection 3498 | |
Z1619 | Resistance to other specified beta lactam antibiotics |
PDX Collection 3499 | |
E7871 | Barth syndrome |
E7872 | Smith-Lemli-Opitz syndrome |
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's syndrome, unspecified |
Q87410 | Marfan's syndrome with aortic dilation |
Q87418 | Marfan's syndrome with other cardiovascular manifestations |
Q8742 | Marfan's syndrome with ocular manifestations |
Q8743 | Marfan's syndrome with skeletal manifestation |
Q875 | Other congenital malformation syndromes with other skeletal changes |
Q8781 | Alport syndrome |
Q8782 | Arterial tortuosity syndrome |
Q8789 | Other specified congenital malformation syndromes, not elsewhere classified |
Q898 | Other specified congenital malformations |
Q992 | Fragile X chromosome |
PDX Collection 3501 | |
E7871 | Barth syndrome |
E7872 | Smith-Lemli-Opitz syndrome |
G901 | Familial dysautonomia [Riley-Day] |
Q050 | Cervical spina bifida with hydrocephalus |
Q051 | Thoracic spina bifida with hydrocephalus |
Q052 | Lumbar spina bifida with hydrocephalus |
Q053 | Sacral spina bifida with hydrocephalus |
Q054 | Unspecified spina bifida with hydrocephalus |
Q055 | Cervical spina bifida without hydrocephalus |
Q056 | Thoracic spina bifida without hydrocephalus |
Q057 | Lumbar spina bifida without hydrocephalus |
Q058 | Sacral spina bifida without hydrocephalus |
Q059 | Spina bifida, unspecified |
Q060 | Amyelia |
Q061 | Hypoplasia and dysplasia of spinal cord |
Q063 | Other congenital cauda equina malformations |
Q068 | Other specified congenital malformations of spinal cord |
Q069 | Congenital malformation of spinal cord, unspecified |
Q0700 | Arnold-Chiari syndrome without spina bifida or hydrocephalus |
Q0701 | Arnold-Chiari syndrome with spina bifida |
Q0702 | Arnold-Chiari syndrome with hydrocephalus |
Q0703 | Arnold-Chiari syndrome with spina bifida and hydrocephalus |
Q078 | Other specified congenital malformations of nervous system |
Q079 | Congenital malformation of nervous 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's syndrome, unspecified |
Q87410 | Marfan's syndrome with aortic dilation |
Q87418 | Marfan's syndrome with other cardiovascular manifestations |
Q8742 | Marfan's syndrome with ocular manifestations |
Q8743 | Marfan's syndrome with skeletal manifestation |
Q875 | Other congenital malformation syndromes with other skeletal changes |
Q8781 | Alport syndrome |
Q8782 | Arterial tortuosity 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 3503 | |
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 |
Q220 | Pulmonary valve atresia |
Q221 | Congenital pulmonary valve stenosis |
Q222 | Congenital pulmonary valve insufficiency |
Q223 | Other congenital malformations of pulmonary valve |
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's syndrome, unspecified |
Q87410 | Marfan's syndrome with aortic dilation |
Q87418 | Marfan's syndrome with other cardiovascular manifestations |
Q8742 | Marfan's syndrome with ocular manifestations |
Q8743 | Marfan's syndrome with skeletal manifestation |
Q875 | Other congenital malformation syndromes with other skeletal changes |
Q8781 | Alport syndrome |
Q8782 | Arterial tortuosity 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 3504 | |
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's syndrome, unspecified |
Q87410 | Marfan's syndrome with aortic dilation |
Q87418 | Marfan's syndrome with other cardiovascular manifestations |
Q8742 | Marfan's syndrome with ocular manifestations |
Q8743 | Marfan's syndrome with skeletal manifestation |
Q875 | Other congenital malformation syndromes with other skeletal changes |
Q8781 | Alport syndrome |
Q8782 | Arterial tortuosity 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 3505 | |
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 |
Q238 | Other congenital malformations of aortic and mitral valves |
Q239 | Congenital malformation of aortic and mitral valves, unspecified |
Q242 | Cor triatriatum |
Q243 | Pulmonary infundibular stenosis |
Q244 | Congenital subaortic stenosis |
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's syndrome, unspecified |
Q87410 | Marfan's syndrome with aortic dilation |
Q87418 | Marfan's syndrome with other cardiovascular manifestations |
Q8742 | Marfan's syndrome with ocular manifestations |
Q8743 | Marfan's syndrome with skeletal manifestation |
Q875 | Other congenital malformation syndromes with other skeletal changes |
Q8781 | Alport syndrome |
Q8782 | Arterial tortuosity 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 3506 | |
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 |
Q238 | Other congenital malformations of aortic and mitral valves |
Q239 | Congenital malformation of aortic and mitral valves, unspecified |
Q246 | Congenital heart block |
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's syndrome, unspecified |
Q87410 | Marfan's syndrome with aortic dilation |
Q87418 | Marfan's syndrome with other cardiovascular manifestations |
Q8742 | Marfan's syndrome with ocular manifestations |
Q8743 | Marfan's syndrome with skeletal manifestation |
Q875 | Other congenital malformation syndromes with other skeletal changes |
Q8781 | Alport syndrome |
Q8782 | Arterial tortuosity 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 3507 | |
E7871 | Barth syndrome |
E7872 | Smith-Lemli-Opitz syndrome |
P2930 | Pulmonary hypertension of newborn |
P2938 | Other persistent fetal circulation |
Q251 | Coarctation of aorta |
Q2521 | Interruption of aortic arch |
Q2529 | Other atresia of aorta |
Q253 | Supravalvular aortic stenosis |
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's syndrome, unspecified |
Q87410 | Marfan's syndrome with aortic dilation |
Q87418 | Marfan's syndrome with other cardiovascular manifestations |
Q8742 | Marfan's syndrome with ocular manifestations |
Q8743 | Marfan's syndrome with skeletal manifestation |
Q875 | Other congenital malformation syndromes with other skeletal changes |
Q8781 | Alport syndrome |
Q8782 | Arterial tortuosity 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 3595 | |
I161 | Hypertensive emergency |
PDX Collection 3596 | |
I169 | Hypertensive crisis, unspecified |
PDX Collection 3600 | |
J948 | Other specified pleural conditions |
PDX Collection 3601 | |
S06370A | Contusion, laceration, and hemorrhage of cerebellum without loss of consciousness, initial encounter |
PDX Collection 3602 | |
S06380A | Contusion, laceration, and hemorrhage of brainstem without loss of consciousness, initial encounter |
PDX Collection 3604 | |
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 |
A212 | Pulmonary tularemia |
A221 | Pulmonary anthrax |
A310 | Pulmonary mycobacterial infection |
A3701 | Whooping cough due to Bordetella pertussis with pneumonia |
A3711 | Whooping cough due to Bordetella parapertussis with pneumonia |
A3781 | Whooping cough due to other Bordetella species with pneumonia |
A3791 | Whooping cough, unspecified species with pneumonia |
A420 | Pulmonary actinomycosis |
A430 | Pulmonary nocardiosis |
A481 | Legionnaires' disease |
B250 | Cytomegaloviral pneumonitis |
B390 | Acute pulmonary histoplasmosis capsulati |
B391 | Chronic pulmonary histoplasmosis capsulati |
B392 | Pulmonary histoplasmosis capsulati, unspecified |
B440 | Invasive pulmonary aspergillosis |
B583 | Pulmonary toxoplasmosis |
B59 | Pneumocystosis |
B671 | Echinococcus granulosus infection of lung |
J09X1 | Influenza due to identified novel influenza A virus with pneumonia |
J09X2 | Influenza due to identified novel influenza A virus with other respiratory manifestations |
J1000 | Influenza due to other identified influenza virus with unspecified type of pneumonia |
J1001 | Influenza due to other identified influenza virus with the same other identified influenza virus pneumonia |
J1008 | Influenza due to other identified influenza virus with other specified pneumonia |
J101 | Influenza due to other identified influenza virus with other respiratory manifestations |
J1100 | Influenza due to unidentified influenza virus with unspecified type of pneumonia |
J1108 | Influenza due to unidentified influenza virus with specified pneumonia |
J111 | Influenza due to unidentified influenza virus with other respiratory manifestations |
J120 | Adenoviral pneumonia |
J121 | Respiratory syncytial virus pneumonia |
J122 | Parainfluenza virus pneumonia |
J123 | Human metapneumovirus pneumonia |
J1289 | Other viral pneumonia |
J129 | Viral pneumonia, unspecified |
J13 | Pneumonia due to Streptococcus pneumoniae |
J14 | Pneumonia due to Hemophilus influenzae |
J150 | Pneumonia due to Klebsiella pneumoniae |
J151 | Pneumonia due to Pseudomonas |
J1520 | Pneumonia due to staphylococcus, unspecified |
J15211 | Pneumonia due to Methicillin susceptible Staphylococcus aureus |
J15212 | Pneumonia due to Methicillin resistant Staphylococcus aureus |
J1529 | Pneumonia due to other staphylococcus |
J153 | Pneumonia due to streptococcus, group B |
J154 | Pneumonia due to other streptococci |
J155 | Pneumonia due to Escherichia coli |
J156 | Pneumonia due to other Gram-negative bacteria |
J157 | Pneumonia due to Mycoplasma pneumoniae |
J158 | Pneumonia due to other specified bacteria |
J159 | Unspecified bacterial pneumonia |
J160 | Chlamydial pneumonia |
J168 | Pneumonia due to other specified infectious organisms |
J17 | Pneumonia in diseases classified elsewhere |
J180 | Bronchopneumonia, unspecified organism |
J181 | Lobar pneumonia, unspecified organism |
J188 | Other pneumonia, unspecified organism |
J189 | Pneumonia, unspecified organism |
J22 | Unspecified acute lower respiratory infection |
J449 | Chronic obstructive pulmonary disease, unspecified |
J470 | Bronchiectasis with acute lower respiratory infection |
J471 | Bronchiectasis with (acute) exacerbation |
J479 | Bronchiectasis, uncomplicated |
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 |
J984 | Other disorders of lung |
J988 | Other specified respiratory disorders |
J989 | Respiratory disorder, unspecified |
J99 | Respiratory disorders in diseases classified elsewhere |
Q334 | Congenital bronchiectasis |
R911 | Solitary pulmonary nodule |
U070 | Vaping-related disorder |
PDX Collection 3605 | |
G43601 | Persistent migraine aura with cerebral infarction, not intractable, with status migrainosus |
G43609 | Persistent migraine aura with cerebral infarction, not intractable, without status migrainosus |
G43611 | Persistent migraine aura with cerebral infarction, intractable, with status migrainosus |
G43619 | Persistent migraine aura with cerebral infarction, intractable, without status migrainosus |
I6300 | Cerebral infarction due to thrombosis of unspecified precerebral artery |
I63011 | Cerebral infarction due to thrombosis of right vertebral artery |
I63012 | Cerebral infarction due to thrombosis of left vertebral artery |
I63013 | Cerebral infarction due to thrombosis of bilateral vertebral arteries |
I63019 | Cerebral infarction due to thrombosis of unspecified vertebral artery |
I6302 | Cerebral infarction due to thrombosis of basilar artery |
I63031 | Cerebral infarction due to thrombosis of right carotid artery |
I63032 | Cerebral infarction due to thrombosis of left carotid artery |
I63033 | Cerebral infarction due to thrombosis of bilateral carotid arteries |
I63039 | Cerebral infarction due to thrombosis of unspecified carotid artery |
I6309 | Cerebral infarction due to thrombosis of other precerebral artery |
I6310 | Cerebral infarction due to embolism of unspecified precerebral artery |
I63111 | Cerebral infarction due to embolism of right vertebral artery |
I63112 | Cerebral infarction due to embolism of left vertebral artery |
I63113 | Cerebral infarction due to embolism of bilateral vertebral arteries |
I63119 | Cerebral infarction due to embolism of unspecified vertebral artery |
I6312 | Cerebral infarction due to embolism of basilar artery |
I63131 | Cerebral infarction due to embolism of right carotid artery |
I63132 | Cerebral infarction due to embolism of left carotid artery |
I63133 | Cerebral infarction due to embolism of bilateral carotid arteries |
I63139 | Cerebral infarction due to embolism of unspecified carotid artery |
I6319 | Cerebral infarction due to embolism of other precerebral artery |
I6320 | Cerebral infarction due to unspecified occlusion or stenosis of unspecified precerebral arteries |
I63211 | Cerebral infarction due to unspecified occlusion or stenosis of right vertebral artery |
I63212 | Cerebral infarction due to unspecified occlusion or stenosis of left vertebral artery |
I63213 | Cerebral infarction due to unspecified occlusion or stenosis of bilateral vertebral arteries |
I63219 | Cerebral infarction due to unspecified occlusion or stenosis of unspecified vertebral artery |
I6322 | Cerebral infarction due to unspecified occlusion or stenosis of basilar artery |
I63231 | Cerebral infarction due to unspecified occlusion or stenosis of right carotid arteries |
Centers for Medicare & Medicaid Services, 7500 Security Boulevard Baltimore, MD 21244 16 Mar 2022 17:08:13 CMS, code-revision=333, description-revision=1331 |