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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 1194 of 1375 |
PDX Collection 6357 (continued) | |
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 |
E88810 | Metabolic syndrome |
PDX Collection 6358 | |
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 |
E88810 | Metabolic syndrome |
PDX Collection 6359 | |
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 |
E88810 | Metabolic syndrome |
PDX Collection 6360 | |
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 |
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 6361 | |
E7500 | GM2 gangliosidosis, unspecified |
E7501 | Sandhoff disease |
E7502 | Tay-Sachs disease |
E7509 | Other GM2 gangliosidosis |
E7510 | Unspecified gangliosidosis |
E7511 | Mucolipidosis IV |
E7519 | Other gangliosidosis |
E754 | Neuronal ceroid lipofuscinosis |
F842 | Rett's syndrome |
G132 | Systemic atrophy primarily affecting the central nervous system in myxedema |
G138 | Systemic atrophy primarily affecting central nervous system in other diseases classified elsewhere |
G300 | Alzheimer's disease with early onset |
G301 | Alzheimer's disease with late onset |
G308 | Other Alzheimer's disease |
G309 | Alzheimer's disease, unspecified |
G3101 | Pick's disease |
G3109 | Other frontotemporal neurocognitive disorder |
G311 | Senile degeneration of brain, not elsewhere classified |
G312 | Degeneration of nervous system due to alcohol |
G3180 | Leukodystrophy, unspecified |
G3181 | Alpers disease |
G3182 | Leigh's disease |
G3184 | Mild cognitive impairment of uncertain or unknown etiology |
G3185 | Corticobasal degeneration |
G3186 | Alexander disease |
G3189 | Other specified degenerative diseases of nervous system |
G319 | Degenerative disease of nervous system, unspecified |
G914 | Hydrocephalus in diseases classified elsewhere |
G94 | Other disorders of brain in diseases classified elsewhere |
PDX Collection 6362 | |
E7500 | GM2 gangliosidosis, unspecified |
E7501 | Sandhoff disease |
E7502 | Tay-Sachs disease |
E7509 | Other GM2 gangliosidosis |
E7510 | Unspecified gangliosidosis |
E7511 | Mucolipidosis IV |
E7519 | Other gangliosidosis |
E754 | Neuronal ceroid lipofuscinosis |
F842 | Rett's syndrome |
G132 | Systemic atrophy primarily affecting the central nervous system in myxedema |
G138 | Systemic atrophy primarily affecting central nervous system in other diseases classified elsewhere |
G300 | Alzheimer's disease with early onset |
G301 | Alzheimer's disease with late onset |
G308 | Other Alzheimer's disease |
G309 | Alzheimer's disease, unspecified |
G3101 | Pick's disease |
G3109 | Other frontotemporal neurocognitive disorder |
G311 | Senile degeneration of brain, not elsewhere classified |
G312 | Degeneration of nervous system due to alcohol |
G3180 | Leukodystrophy, unspecified |
G3181 | Alpers disease |
G3182 | Leigh's disease |
G3184 | Mild cognitive impairment of uncertain or unknown etiology |
G3185 | Corticobasal degeneration |
G3186 | Alexander disease |
G3189 | Other specified degenerative diseases of nervous system |
G319 | Degenerative disease of nervous system, unspecified |
G914 | Hydrocephalus in diseases classified elsewhere |
G94 | Other disorders of brain in diseases classified elsewhere |
PDX Collection 6363 | |
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 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 6364 | |
D474 | Osteomyelofibrosis |
D500 | Iron deficiency anemia secondary to blood loss (chronic) |
D501 | Sideropenic dysphagia |
D508 | Other iron deficiency anemias |
D509 | Iron deficiency anemia, unspecified |
D510 | Vitamin B12 deficiency anemia due to intrinsic factor deficiency |
D511 | Vitamin B12 deficiency anemia due to selective vitamin B12 malabsorption with proteinuria |
D512 | Transcobalamin II deficiency |
D513 | Other dietary vitamin B12 deficiency anemia |
D518 | Other vitamin B12 deficiency anemias |
D519 | Vitamin B12 deficiency anemia, unspecified |
D520 | Dietary folate deficiency anemia |
D521 | Drug-induced folate deficiency anemia |
D528 | Other folate deficiency anemias |
D529 | Folate deficiency anemia, unspecified |
D530 | Protein deficiency anemia |
D531 | Other megaloblastic anemias, not elsewhere classified |
D532 | Scorbutic anemia |
D538 | Other specified nutritional anemias |
D539 | Nutritional anemia, unspecified |
D550 | Anemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency |
D551 | Anemia due to other disorders of glutathione metabolism |
D553 | Anemia due to disorders of nucleotide metabolism |
D558 | Other anemias due to enzyme disorders |
D559 | Anemia due to enzyme disorder, unspecified |
D560 | Alpha thalassemia |
D561 | Beta thalassemia |
D562 | Delta-beta thalassemia |
D563 | Thalassemia minor |
D564 | Hereditary persistence of fetal hemoglobin [HPFH] |
D565 | Hemoglobin E-beta thalassemia |
D568 | Other thalassemias |
D569 | Thalassemia, unspecified |
D5700 | Hb-SS disease with crisis, unspecified |
D5701 | Hb-SS disease with acute chest syndrome |
D5702 | Hb-SS disease with splenic sequestration |
D571 | Sickle-cell disease without crisis |
D5720 | Sickle-cell/Hb-C disease without crisis |
D57211 | Sickle-cell/Hb-C disease with acute chest syndrome |
D57212 | Sickle-cell/Hb-C disease with splenic sequestration |
D57213 | Sickle-cell/Hb-C disease with cerebral vascular involvement |
D57214 | Sickle-cell/Hb-C disease with dactylitis |
D57218 | Sickle-cell/Hb-C disease with crisis with other specified complication |
D57219 | Sickle-cell/Hb-C disease with crisis, unspecified |
D573 | Sickle-cell trait |
D5740 | Sickle-cell thalassemia without crisis |
D57411 | Sickle-cell thalassemia, unspecified, with acute chest syndrome |
D57412 | Sickle-cell thalassemia, unspecified, with splenic sequestration |
D57419 | Sickle-cell thalassemia, unspecified, with crisis |
D5780 | Other sickle-cell disorders without crisis |
D57811 | Other sickle-cell disorders with acute chest syndrome |
D57812 | Other sickle-cell disorders with splenic sequestration |
D57819 | Other sickle-cell disorders with crisis, unspecified |
D580 | Hereditary spherocytosis |
D581 | Hereditary elliptocytosis |
D582 | Other hemoglobinopathies |
D588 | Other specified hereditary hemolytic anemias |
D589 | Hereditary hemolytic anemia, unspecified |
D590 | Drug-induced autoimmune hemolytic anemia |
D5910 | Autoimmune hemolytic anemia, unspecified |
D5911 | Warm autoimmune hemolytic anemia |
D5912 | Cold autoimmune hemolytic anemia |
D5913 | Mixed type autoimmune hemolytic anemia |
D5919 | Other autoimmune hemolytic anemia |
D592 | Drug-induced nonautoimmune hemolytic anemia |
D5930 | Hemolytic-uremic syndrome, unspecified |
D5931 | Infection-associated hemolytic-uremic syndrome |
D5932 | Hereditary hemolytic-uremic syndrome |
D5939 | Other hemolytic-uremic syndrome |
D594 | Other nonautoimmune hemolytic anemias |
D595 | Paroxysmal nocturnal hemoglobinuria [Marchiafava-Micheli] |
D596 | Hemoglobinuria due to hemolysis from other external causes |
D598 | Other acquired hemolytic anemias |
D599 | Acquired hemolytic anemia, unspecified |
D600 | Chronic acquired pure red cell aplasia |
D601 | Transient acquired pure red cell aplasia |
D608 | Other acquired pure red cell aplasias |
D609 | Acquired pure red cell aplasia, unspecified |
D6101 | Constitutional (pure) red blood cell aplasia |
D6102 | Shwachman-Diamond syndrome |
D6109 | Other constitutional aplastic anemia |
D611 | Drug-induced aplastic anemia |
D612 | Aplastic anemia due to other external agents |
D613 | Idiopathic aplastic anemia |
D61810 | Antineoplastic chemotherapy induced pancytopenia |
D61811 | Other drug-induced pancytopenia |
D61818 | Other pancytopenia |
Centers for Medicare & Medicaid Services, 7500 Security Boulevard Baltimore, MD 21244 01 Mar 2023 06:12:40 CMS, code-revision=344, description-revision=1357 |