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 1273 of 1375 |
| PDX Collection 6690 (continued) | |
| E7629 | Other mucopolysaccharidoses |
| E763 | Mucopolysaccharidosis, unspecified |
| E768 | Other disorders of glucosaminoglycan metabolism |
| E769 | Glucosaminoglycan metabolism disorder, unspecified |
| E791 | Lesch-Nyhan syndrome |
| E792 | Myoadenylate deaminase deficiency |
| E7981 | Aicardi-Goutières syndrome |
| E7982 | Hereditary xanthinuria |
| E7989 | Other specified disorders of purine and pyrimidine metabolism |
| E799 | Disorder of purine and pyrimidine metabolism, unspecified |
| E800 | Hereditary erythropoietic porphyria |
| E801 | Porphyria cutanea tarda |
| E8020 | Unspecified porphyria |
| E8021 | Acute intermittent (hepatic) porphyria |
| E8029 | Other porphyria |
| E804 | Gilbert syndrome |
| E805 | Crigler-Najjar syndrome |
| E806 | Other disorders of bilirubin metabolism |
| E807 | Disorder of bilirubin metabolism, unspecified |
| E850 | Non-neuropathic heredofamilial amyloidosis |
| E859 | Amyloidosis, unspecified |
| E88810 | Metabolic syndrome |
| PDX Collection 6691 | |
| E0840 | Diabetes mellitus due to underlying condition with diabetic neuropathy, unspecified |
| E0841 | Diabetes mellitus due to underlying condition with diabetic mononeuropathy |
| E0842 | Diabetes mellitus due to underlying condition with diabetic polyneuropathy |
| E0843 | Diabetes mellitus due to underlying condition with diabetic autonomic (poly)neuropathy |
| E0844 | Diabetes mellitus due to underlying condition with diabetic amyotrophy |
| E0849 | Diabetes mellitus due to underlying condition with other diabetic neurological complication |
| E0940 | Drug or chemical induced diabetes mellitus with neurological complications with diabetic neuropathy, unspecified |
| E0941 | Drug or chemical induced diabetes mellitus with neurological complications with diabetic mononeuropathy |
| E0942 | Drug or chemical induced diabetes mellitus with neurological complications with diabetic polyneuropathy |
| E0943 | Drug or chemical induced diabetes mellitus with neurological complications with diabetic autonomic (poly)neuropathy |
| E0944 | Drug or chemical induced diabetes mellitus with neurological complications with diabetic amyotrophy |
| E0949 | Drug or chemical induced diabetes mellitus with neurological complications with other diabetic neurological complication |
| E1040 | Type 1 diabetes mellitus with diabetic neuropathy, unspecified |
| E1041 | Type 1 diabetes mellitus with diabetic mononeuropathy |
| E1042 | Type 1 diabetes mellitus with diabetic polyneuropathy |
| E1043 | Type 1 diabetes mellitus with diabetic autonomic (poly)neuropathy |
| E1044 | Type 1 diabetes mellitus with diabetic amyotrophy |
| E1049 | Type 1 diabetes mellitus with other diabetic neurological complication |
| E1140 | Type 2 diabetes mellitus with diabetic neuropathy, unspecified |
| E1141 | Type 2 diabetes mellitus with diabetic mononeuropathy |
| E1142 | Type 2 diabetes mellitus with diabetic polyneuropathy |
| E1143 | Type 2 diabetes mellitus with diabetic autonomic (poly)neuropathy |
| E1144 | Type 2 diabetes mellitus with diabetic amyotrophy |
| E1149 | Type 2 diabetes mellitus with other diabetic neurological complication |
| E1340 | Other specified diabetes mellitus with diabetic neuropathy, unspecified |
| E1341 | Other specified diabetes mellitus with diabetic mononeuropathy |
| E1342 | Other specified diabetes mellitus with diabetic polyneuropathy |
| E1343 | Other specified diabetes mellitus with diabetic autonomic (poly)neuropathy |
| E1344 | Other specified diabetes mellitus with diabetic amyotrophy |
| E1349 | Other specified diabetes mellitus with other diabetic neurological complication |
| G3289 | Other specified degenerative disorders of nervous system in diseases classified elsewhere |
| G40001 | Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, not intractable, with status epilepticus |
| G40009 | Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, not intractable, without status epilepticus |
| G40011 | Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, intractable, with status epilepticus |
| G40019 | Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, intractable, without status epilepticus |
| G40101 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, not intractable, with status epilepticus |
| G40109 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, not intractable, without status epilepticus |
| G40111 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, intractable, with status epilepticus |
| G40119 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, intractable, without status epilepticus |
| G40201 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, not intractable, with status epilepticus |
| G40209 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, not intractable, without status epilepticus |
| G40211 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, intractable, with status epilepticus |
| G40219 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, intractable, without status epilepticus |
| G40301 | Generalized idiopathic epilepsy and epileptic syndromes, not intractable, with status epilepticus |
| G40309 | Generalized idiopathic epilepsy and epileptic syndromes, not intractable, without status epilepticus |
| G40311 | Generalized idiopathic epilepsy and epileptic syndromes, intractable, with status epilepticus |
| G40319 | Generalized idiopathic epilepsy and epileptic syndromes, intractable, without status epilepticus |
| G40401 | Other generalized epilepsy and epileptic syndromes, not intractable, with status epilepticus |
| G40409 | Other generalized epilepsy and epileptic syndromes, not intractable, without status epilepticus |
| G40411 | Other generalized epilepsy and epileptic syndromes, intractable, with status epilepticus |
| G40419 | Other generalized epilepsy and epileptic syndromes, intractable, without status epilepticus |
| G4042 | Cyclin-Dependent Kinase-Like 5 Deficiency Disorder |
| G40501 | Epileptic seizures related to external causes, not intractable, with status epilepticus |
| G40509 | Epileptic seizures related to external causes, not intractable, without status epilepticus |
| G40801 | Other epilepsy, not intractable, with status epilepticus |
| G40802 | Other epilepsy, not intractable, without status epilepticus |
| G40803 | Other epilepsy, intractable, with status epilepticus |
| G40804 | Other epilepsy, intractable, without status epilepticus |
| G40811 | Lennox-Gastaut syndrome, not intractable, with status epilepticus |
| G40812 | Lennox-Gastaut syndrome, not intractable, without status epilepticus |
| G40813 | Lennox-Gastaut syndrome, intractable, with status epilepticus |
| G40814 | Lennox-Gastaut syndrome, intractable, without status epilepticus |
| G40821 | Epileptic spasms, not intractable, with status epilepticus |
| G40822 | Epileptic spasms, not intractable, without status epilepticus |
| G40823 | Epileptic spasms, intractable, with status epilepticus |
| G40824 | Epileptic spasms, intractable, without status epilepticus |
| G40833 | Dravet syndrome, intractable, with status epilepticus |
| G40834 | Dravet syndrome, intractable, without status epilepticus |
| G4089 | Other seizures |
| G40901 | Epilepsy, unspecified, not intractable, with status epilepticus |
| G40909 | Epilepsy, unspecified, not intractable, without status epilepticus |
| G40911 | Epilepsy, unspecified, intractable, with status epilepticus |
| G40919 | Epilepsy, unspecified, intractable, without status epilepticus |
| G40A01 | Absence epileptic syndrome, not intractable, with status epilepticus |
| G40A09 | Absence epileptic syndrome, not intractable, without status epilepticus |
| G40A11 | Absence epileptic syndrome, intractable, with status epilepticus |
| G40A19 | Absence epileptic syndrome, intractable, without status epilepticus |
| G40B01 | Juvenile myoclonic epilepsy, not intractable, with status epilepticus |
| G40B09 | Juvenile myoclonic epilepsy, not intractable, without status epilepticus |
| G40B11 | Juvenile myoclonic epilepsy, intractable, with status epilepticus |
| G40B19 | Juvenile myoclonic epilepsy, intractable, without status epilepticus |
| G40C01 | Lafora progressive myoclonus epilepsy, not intractable, with status epilepticus |
| G40C09 | Lafora progressive myoclonus epilepsy, not intractable, without status epilepticus |
| G40C11 | Lafora progressive myoclonus epilepsy, intractable, with status epilepticus |
| G40C19 | Lafora progressive myoclonus epilepsy, intractable, without status epilepticus |
| G9381 | Temporal sclerosis |
| G9389 | Other specified disorders of brain |
| G939 | Disorder of brain, unspecified |
| G969 | Disorder of central nervous system, unspecified |
| G980 | Neurogenic arthritis, not elsewhere classified |
| G988 | Other disorders of nervous system |
| G998 | Other specified disorders of nervous system in diseases classified elsewhere |
| R561 | Post traumatic seizures |
| PDX Collection 6692 | |
| E7871 | Barth syndrome |
| E7872 | Smith-Lemli-Opitz syndrome |
| Q8581 | PTEN tumor syndrome |
| Q8582 | Other Cowden syndrome |
| Q8583 | Von Hippel-Lindau syndrome |
| Q8589 | Other phakomatoses, not elsewhere classified |
| Q859 | Phakomatosis, 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 |
| Q899 | Congenital malformation, unspecified |
| Q992 | Fragile X chromosome |
| PDX Collection 6693 | |
| D8130 | Adenosine deaminase deficiency, unspecified |
| D8131 | Severe combined immunodeficiency due to adenosine deaminase deficiency |
| D8132 | Adenosine deaminase 2 deficiency |
| D8139 | Other adenosine deaminase deficiency |
| D815 | Purine nucleoside phosphorylase [PNP] deficiency |
| D81810 | Biotinidase deficiency |
| D841 | Defects in the complement system |
| E7601 | Hurler's syndrome |
| E7602 | Hurler-Scheie syndrome |
| E7603 | Scheie's syndrome |
| E761 | Mucopolysaccharidosis, type II |
| E76210 | Morquio A mucopolysaccharidoses |
| E76211 | Morquio B mucopolysaccharidoses |
| E76219 | Morquio mucopolysaccharidoses, unspecified |
| E7622 | Sanfilippo mucopolysaccharidoses |
| E7629 | Other mucopolysaccharidoses |
| E763 | Mucopolysaccharidosis, unspecified |
| E768 | Other disorders of glucosaminoglycan metabolism |
| E769 | Glucosaminoglycan metabolism disorder, unspecified |
| E791 | Lesch-Nyhan syndrome |
| E792 | Myoadenylate deaminase deficiency |
| E7981 | Aicardi-Goutières syndrome |
| E7982 | Hereditary xanthinuria |
| E7989 | Other specified disorders of purine and pyrimidine metabolism |
| E799 | Disorder of purine and pyrimidine metabolism, unspecified |
| E800 | Hereditary erythropoietic porphyria |
| E801 | Porphyria cutanea tarda |
| E8020 | Unspecified porphyria |
| E8021 | Acute intermittent (hepatic) porphyria |
| E8029 | Other porphyria |
| E804 | Gilbert syndrome |
| E805 | Crigler-Najjar syndrome |
| E806 | Other disorders of bilirubin metabolism |
| E807 | Disorder of bilirubin metabolism, unspecified |
| E850 | Non-neuropathic heredofamilial amyloidosis |
| E859 | Amyloidosis, unspecified |
| E88810 | Metabolic syndrome |
| PDX Collection 6694 | |
| E7871 | Barth syndrome |
| E7872 | Smith-Lemli-Opitz syndrome |
| Q8581 | PTEN tumor syndrome |
| Q8582 | Other Cowden syndrome |
| Q8583 | Von Hippel-Lindau syndrome |
| Q8589 | Other phakomatoses, not elsewhere classified |
| Q859 | Phakomatosis, 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 |
| Q899 | Congenital malformation, unspecified |
| Q992 | Fragile X chromosome |
| PDX Collection 6695 | |
| D8130 | Adenosine deaminase deficiency, unspecified |
| D8131 | Severe combined immunodeficiency due to adenosine deaminase deficiency |
| D8132 | Adenosine deaminase 2 deficiency |
| D8139 | Other adenosine deaminase deficiency |
| D815 | Purine nucleoside phosphorylase [PNP] deficiency |
| D81810 | Biotinidase deficiency |
| D841 | Defects in the complement system |
| E7601 | Hurler's syndrome |
| E7602 | Hurler-Scheie syndrome |
| E7603 | Scheie's syndrome |
| E761 | Mucopolysaccharidosis, type II |
| E76210 | Morquio A mucopolysaccharidoses |
| E76211 | Morquio B mucopolysaccharidoses |
| E76219 | Morquio mucopolysaccharidoses, unspecified |
| E7622 | Sanfilippo mucopolysaccharidoses |
| E7629 | Other mucopolysaccharidoses |
| E763 | Mucopolysaccharidosis, unspecified |
| E768 | Other disorders of glucosaminoglycan metabolism |
| E769 | Glucosaminoglycan metabolism disorder, unspecified |
| E791 | Lesch-Nyhan syndrome |
| E792 | Myoadenylate deaminase deficiency |
| E7981 | Aicardi-Goutières syndrome |
| E7982 | Hereditary xanthinuria |
| E7989 | Other specified disorders of purine and pyrimidine metabolism |
| E799 | Disorder of purine and pyrimidine metabolism, unspecified |
| E800 | Hereditary erythropoietic porphyria |
| E801 | Porphyria cutanea tarda |
| E8020 | Unspecified porphyria |
| E8021 | Acute intermittent (hepatic) porphyria |
| E8029 | Other porphyria |
| E804 | Gilbert syndrome |
| E805 | Crigler-Najjar syndrome |
| E806 | Other disorders of bilirubin metabolism |
| E807 | Disorder of bilirubin metabolism, unspecified |
| E850 | Non-neuropathic heredofamilial amyloidosis |
| E859 | Amyloidosis, unspecified |
| E88810 | Metabolic syndrome |
| PDX Collection 6696 | |
| E7871 | Barth syndrome |
| E7872 | Smith-Lemli-Opitz syndrome |
| Q8581 | PTEN tumor syndrome |
| Q8582 | Other Cowden syndrome |
| Q8583 | Von Hippel-Lindau syndrome |
| Q8589 | Other phakomatoses, not elsewhere classified |
| Q859 | Phakomatosis, 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 |
| Q899 | Congenital malformation, unspecified |
| Q992 | Fragile X chromosome |
| PDX Collection 6697 | |
| 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 |
| J1561 | Pneumonia due to Acinetobacter baumannii |
| J1569 | 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 |
| 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 |
| 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 |
|
Centers for Medicare & Medicaid Services, 7500 Security Boulevard Baltimore, MD 21244 01 Mar 2023 06:12:40 CMS, code-revision=344, description-revision=1357 |