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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 1244 of 1375 |
PDX Collection 6559 (continued) | |
E7142 | Carnitine deficiency due to inborn errors of metabolism |
E7143 | Iatrogenic carnitine deficiency |
E71440 | Ruvalcaba-Myhre-Smith syndrome |
E71448 | Other secondary carnitine deficiency |
E71540 | Rhizomelic chondrodysplasia punctata |
E803 | Defects of catalase and peroxidase |
E804 | Gilbert syndrome |
E805 | Crigler-Najjar syndrome |
E806 | Other disorders of bilirubin metabolism |
E807 | Disorder of bilirubin metabolism, unspecified |
E8840 | Mitochondrial metabolism disorder, unspecified |
E8841 | MELAS syndrome |
E8842 | MERRF syndrome |
E8843 | Disorders of mitochondrial tRNA synthetases |
E8849 | Other mitochondrial metabolism disorders |
E88811 | Insulin resistance syndrome, Type A |
E88818 | Other insulin resistance |
E88819 | Insulin resistance, unspecified |
E8889 | Other specified metabolic disorders |
H49811 | Kearns-Sayre syndrome, right eye |
H49812 | Kearns-Sayre syndrome, left eye |
H49813 | Kearns-Sayre syndrome, bilateral |
H49819 | Kearns-Sayre syndrome, unspecified eye |
PDX Collection 6560 | |
C965 | Multifocal and unisystemic Langerhans-cell histiocytosis |
C966 | Unifocal Langerhans-cell histiocytosis |
E71310 | Long chain/very long chain acyl CoA dehydrogenase deficiency |
E71311 | Medium chain acyl CoA dehydrogenase deficiency |
E71312 | Short chain acyl CoA dehydrogenase deficiency |
E71313 | Glutaric aciduria type II |
E71314 | Muscle carnitine palmitoyltransferase deficiency |
E71318 | Other disorders of fatty-acid oxidation |
E7132 | Disorders of ketone metabolism |
E7139 | Other disorders of fatty-acid metabolism |
E7140 | Disorder of carnitine metabolism, unspecified |
E7141 | Primary carnitine deficiency |
E7142 | Carnitine deficiency due to inborn errors of metabolism |
E7143 | Iatrogenic carnitine deficiency |
E71440 | Ruvalcaba-Myhre-Smith syndrome |
E71448 | Other secondary carnitine deficiency |
E71541 | Zellweger-like syndrome |
E803 | Defects of catalase and peroxidase |
E804 | Gilbert syndrome |
E805 | Crigler-Najjar syndrome |
E806 | Other disorders of bilirubin metabolism |
E807 | Disorder of bilirubin metabolism, unspecified |
E8840 | Mitochondrial metabolism disorder, unspecified |
E8841 | MELAS syndrome |
E8842 | MERRF syndrome |
E8843 | Disorders of mitochondrial tRNA synthetases |
E8849 | Other mitochondrial metabolism disorders |
E88811 | Insulin resistance syndrome, Type A |
E88818 | Other insulin resistance |
E88819 | Insulin resistance, unspecified |
E8889 | Other specified metabolic disorders |
H49811 | Kearns-Sayre syndrome, right eye |
H49812 | Kearns-Sayre syndrome, left eye |
H49813 | Kearns-Sayre syndrome, bilateral |
H49819 | Kearns-Sayre syndrome, unspecified eye |
PDX Collection 6561 | |
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 6562 | |
E8419 | Cystic fibrosis with other intestinal manifestations |
K900 | Celiac disease |
K901 | Tropical sprue |
K902 | Blind loop syndrome, not elsewhere classified |
K903 | Pancreatic steatorrhea |
K9041 | Non-celiac gluten sensitivity |
K9049 | Malabsorption due to intolerance, not elsewhere classified |
K90821 | Short bowel syndrome with colon in continuity |
K90822 | Short bowel syndrome without colon in continuity |
K90829 | Short bowel syndrome, unspecified |
K9083 | Intestinal failure |
K9089 | Other intestinal malabsorption |
K909 | Intestinal malabsorption, unspecified |
K912 | Postsurgical malabsorption, not elsewhere classified |
PDX Collection 6563 | |
Z5900 | Homelessness unspecified |
Z5901 | Sheltered homelessness |
Z5902 | Unsheltered homelessness |
PDX Collection 6564 | |
E8419 | Cystic fibrosis with other intestinal manifestations |
K900 | Celiac disease |
K901 | Tropical sprue |
K902 | Blind loop syndrome, not elsewhere classified |
K903 | Pancreatic steatorrhea |
K9041 | Non-celiac gluten sensitivity |
K9049 | Malabsorption due to intolerance, not elsewhere classified |
K90821 | Short bowel syndrome with colon in continuity |
K90822 | Short bowel syndrome without colon in continuity |
K90829 | Short bowel syndrome, unspecified |
K9083 | Intestinal failure |
K9089 | Other intestinal malabsorption |
K909 | Intestinal malabsorption, unspecified |
K912 | Postsurgical malabsorption, not elsewhere classified |
PDX Collection 6565 | |
Z5900 | Homelessness unspecified |
Z5901 | Sheltered homelessness |
Z5902 | Unsheltered homelessness |
PDX Collection 6566 | |
K560 | Paralytic ileus |
K561 | Intussusception |
K562 | Volvulus |
K563 | Gallstone ileus |
K5649 | Other impaction of intestine |
K5650 | Intestinal adhesions [bands], unspecified as to partial versus complete obstruction |
K5651 | Intestinal adhesions [bands], with partial obstruction |
K5652 | Intestinal adhesions [bands] with complete obstruction |
K56600 | Partial intestinal obstruction, unspecified as to cause |
K56601 | Complete intestinal obstruction, unspecified as to cause |
K56609 | Unspecified intestinal obstruction, unspecified as to partial versus complete obstruction |
K56690 | Other partial intestinal obstruction |
K56691 | Other complete intestinal obstruction |
K56699 | Other intestinal obstruction unspecified as to partial versus complete obstruction |
K567 | Ileus, unspecified |
K634 | Enteroptosis |
K638211 | Small intestinal bacterial overgrowth, hydrogen-subtype |
K638212 | Small intestinal bacterial overgrowth, hydrogen sulfide-subtype |
K638219 | Small intestinal bacterial overgrowth, unspecified |
K63822 | Small intestinal fungal overgrowth |
K63829 | Intestinal methanogen overgrowth, unspecified |
K6389 | Other specified diseases of intestine |
K639 | Disease of intestine, unspecified |
K9130 | Postprocedural intestinal obstruction, unspecified as to partial versus complete |
K9131 | Postprocedural partial intestinal obstruction |
K9132 | Postprocedural complete intestinal obstruction |
K9289 | Other specified diseases of the digestive system |
K929 | Disease of digestive system, unspecified |
R1113 | Vomiting of fecal matter |
PDX Collection 6567 | |
Q900 | Trisomy 21, nonmosaicism (meiotic nondisjunction) |
Q901 | Trisomy 21, mosaicism (mitotic nondisjunction) |
Q902 | Trisomy 21, translocation |
Q909 | Down syndrome, unspecified |
Q910 | Trisomy 18, nonmosaicism (meiotic nondisjunction) |
Q911 | Trisomy 18, mosaicism (mitotic nondisjunction) |
Q912 | Trisomy 18, translocation |
Q913 | Trisomy 18, unspecified |
Q914 | Trisomy 13, nonmosaicism (meiotic nondisjunction) |
Q915 | Trisomy 13, mosaicism (mitotic nondisjunction) |
Q916 | Trisomy 13, translocation |
Q917 | Trisomy 13, unspecified |
Q920 | Whole chromosome trisomy, nonmosaicism (meiotic nondisjunction) |
Q921 | Whole chromosome trisomy, mosaicism (mitotic nondisjunction) |
Q922 | Partial trisomy |
Q925 | Duplications with other complex rearrangements |
Q9261 | Marker chromosomes in normal individual |
Q9262 | Marker chromosomes in abnormal individual |
Q927 | Triploidy and polyploidy |
Q928 | Other specified trisomies and partial trisomies of autosomes |
Q929 | Trisomy and partial trisomy of autosomes, unspecified |
Q930 | Whole chromosome monosomy, nonmosaicism (meiotic nondisjunction) |
Q931 | Whole chromosome monosomy, mosaicism (mitotic nondisjunction) |
Q932 | Chromosome replaced with ring, dicentric or isochromosome |
Q933 | Deletion of short arm of chromosome 4 |
Q934 | Deletion of short arm of chromosome 5 |
Q9351 | Angelman syndrome |
Q9352 | Phelan-McDermid syndrome |
Q9359 | Other deletions of part of a chromosome |
Q937 | Deletions with other complex rearrangements |
Q9381 | Velo-cardio-facial syndrome |
Q9382 | Williams syndrome |
Q9388 | Other microdeletions |
Q9389 | Other deletions from the autosomes |
Q939 | Deletion from autosomes, unspecified |
Q950 | Balanced translocation and insertion in normal individual |
Q951 | Chromosome inversion in normal individual |
Q952 | Balanced autosomal rearrangement in abnormal individual |
Q953 | Balanced sex/autosomal rearrangement in abnormal individual |
Q955 | Individual with autosomal fragile site |
Q958 | Other balanced rearrangements and structural markers |
Q959 | Balanced rearrangement and structural marker, unspecified |
Q960 | Karyotype 45, X |
Q961 | Karyotype 46, X iso (Xq) |
Q962 | Karyotype 46, X with abnormal sex chromosome, except iso (Xq) |
Q963 | Mosaicism, 45, X/46, XX or XY |
Q964 | Mosaicism, 45, X/other cell line(s) with abnormal sex chromosome |
Q968 | Other variants of Turner's syndrome |
Q969 | Turner's syndrome, unspecified |
Q970 | Karyotype 47, XXX |
Q971 | Female with more than three X chromosomes |
Q972 | Mosaicism, lines with various numbers of X chromosomes |
Q973 | Female with 46, XY karyotype |
Q978 | Other specified sex chromosome abnormalities, female phenotype |
Q979 | Sex chromosome abnormality, female phenotype, unspecified |
Q980 | Klinefelter syndrome karyotype 47, XXY |
Q981 | Klinefelter syndrome, male with more than two X chromosomes |
Q983 | Other male with 46, XX karyotype |
Q984 | Klinefelter syndrome, unspecified |
Q985 | Karyotype 47, XYY |
Q986 | Male with structurally abnormal sex chromosome |
Q987 | Male with sex chromosome mosaicism |
Q988 | Other specified sex chromosome abnormalities, male phenotype |
Q989 | Sex chromosome abnormality, male phenotype, unspecified |
Q990 | Chimera 46, XX/46, XY |
Q991 | 46, XX true hermaphrodite |
Q998 | Other specified chromosome abnormalities |
Q999 | Chromosomal abnormality, unspecified |
PDX Collection 6568 | |
K560 | Paralytic ileus |
K561 | Intussusception |
K562 | Volvulus |
K563 | Gallstone ileus |
K5649 | Other impaction of intestine |
K5650 | Intestinal adhesions [bands], unspecified as to partial versus complete obstruction |
K5651 | Intestinal adhesions [bands], with partial obstruction |
K5652 | Intestinal adhesions [bands] with complete obstruction |
K56600 | Partial intestinal obstruction, unspecified as to cause |
K56601 | Complete intestinal obstruction, unspecified as to cause |
K56609 | Unspecified intestinal obstruction, unspecified as to partial versus complete obstruction |
K56690 | Other partial intestinal obstruction |
K56691 | Other complete intestinal obstruction |
K56699 | Other intestinal obstruction unspecified as to partial versus complete obstruction |
K567 | Ileus, unspecified |
K634 | Enteroptosis |
K638211 | Small intestinal bacterial overgrowth, hydrogen-subtype |
K638212 | Small intestinal bacterial overgrowth, hydrogen sulfide-subtype |
K638219 | Small intestinal bacterial overgrowth, unspecified |
K63822 | Small intestinal fungal overgrowth |
K63829 | Intestinal methanogen overgrowth, unspecified |
K6389 | Other specified diseases of intestine |
K639 | Disease of intestine, unspecified |
K9130 | Postprocedural intestinal obstruction, unspecified as to partial versus complete |
K9131 | Postprocedural partial intestinal obstruction |
K9132 | Postprocedural complete intestinal obstruction |
K9289 | Other specified diseases of the digestive system |
K929 | Disease of digestive system, unspecified |
R1113 | Vomiting of fecal matter |
PDX Collection 6569 | |
E8419 | Cystic fibrosis with other intestinal manifestations |
K900 | Celiac disease |
K901 | Tropical sprue |
K902 | Blind loop syndrome, not elsewhere classified |
K903 | Pancreatic steatorrhea |
K9041 | Non-celiac gluten sensitivity |
K9049 | Malabsorption due to intolerance, not elsewhere classified |
K90821 | Short bowel syndrome with colon in continuity |
K90822 | Short bowel syndrome without colon in continuity |
K90829 | Short bowel syndrome, unspecified |
K9083 | Intestinal failure |
K9089 | Other intestinal malabsorption |
K909 | Intestinal malabsorption, unspecified |
K912 | Postsurgical malabsorption, not elsewhere classified |
PDX Collection 6570 | |
Q900 | Trisomy 21, nonmosaicism (meiotic nondisjunction) |
Q901 | Trisomy 21, mosaicism (mitotic nondisjunction) |
Q902 | Trisomy 21, translocation |
Q909 | Down syndrome, unspecified |
Q910 | Trisomy 18, nonmosaicism (meiotic nondisjunction) |
Q911 | Trisomy 18, mosaicism (mitotic nondisjunction) |
Q912 | Trisomy 18, translocation |
Q913 | Trisomy 18, unspecified |
Q914 | Trisomy 13, nonmosaicism (meiotic nondisjunction) |
Q915 | Trisomy 13, mosaicism (mitotic nondisjunction) |
Q916 | Trisomy 13, translocation |
Q917 | Trisomy 13, unspecified |
Q920 | Whole chromosome trisomy, nonmosaicism (meiotic nondisjunction) |
Q921 | Whole chromosome trisomy, mosaicism (mitotic nondisjunction) |
Q922 | Partial trisomy |
Q925 | Duplications with other complex rearrangements |
Q9261 | Marker chromosomes in normal individual |
Q9262 | Marker chromosomes in abnormal individual |
Q927 | Triploidy and polyploidy |
Q928 | Other specified trisomies and partial trisomies of autosomes |
Q929 | Trisomy and partial trisomy of autosomes, unspecified |
Q930 | Whole chromosome monosomy, nonmosaicism (meiotic nondisjunction) |
Q931 | Whole chromosome monosomy, mosaicism (mitotic nondisjunction) |
Q932 | Chromosome replaced with ring, dicentric or isochromosome |
Q933 | Deletion of short arm of chromosome 4 |
Q934 | Deletion of short arm of chromosome 5 |
Q9351 | Angelman syndrome |
Q9352 | Phelan-McDermid syndrome |
Q9359 | Other deletions of part of a chromosome |
Q937 | Deletions with other complex rearrangements |
Q9381 | Velo-cardio-facial syndrome |
Q9382 | Williams syndrome |
Q9388 | Other microdeletions |
Q9389 | Other deletions from the autosomes |
Q939 | Deletion from autosomes, unspecified |
Q950 | Balanced translocation and insertion in normal individual |
Q951 | Chromosome inversion in normal individual |
Q952 | Balanced autosomal rearrangement in abnormal individual |
Centers for Medicare & Medicaid Services, 7500 Security Boulevard Baltimore, MD 21244 01 Mar 2023 06:12:40 CMS, code-revision=344, description-revision=1357 |