ICD-10-CM/PCS MS-DRG v41.0 Definitions Manual

Previous Page [Alt-p] Up a level [Alt-u] Next Page [Alt-n]
Appendix C: Principal diagnoses which convert CC/MCC to non-CC
Page 1198 of 1324
PDX Collection 6550 (continued)
E71121Propionic acidemia
E71128Other disorders of propionate metabolism
E7119Other disorders of branched-chain amino-acid metabolism
E712Disorder of branched-chain amino-acid metabolism, unspecified
E7130Disorder of fatty-acid metabolism, unspecified
E7200Disorders of amino-acid transport, unspecified
E7201Cystinuria
E7202Hartnup's disease
E7204Cystinosis
E7209Other disorders of amino-acid transport
E7210Disorders of sulfur-bearing amino-acid metabolism, unspecified
E7211Homocystinuria
E7212Methylenetetrahydrofolate reductase deficiency
E7219Other disorders of sulfur-bearing amino-acid metabolism
E7220Disorder of urea cycle metabolism, unspecified
E7221Argininemia
E7222Arginosuccinic aciduria
E7223Citrullinemia
E7229Other disorders of urea cycle metabolism
E723Disorders of lysine and hydroxylysine metabolism
E724Disorders of ornithine metabolism
E7250Disorder of glycine metabolism, unspecified
E7251Non-ketotic hyperglycinemia
E7252Trimethylaminuria
E7253Primary hyperoxaluria
E7259Other disorders of glycine metabolism
E7281Disorders of gamma aminobutyric acid metabolism
E7289Other specified disorders of amino-acid metabolism
E729Disorder of amino-acid metabolism, unspecified
E730Congenital lactase deficiency
E731Secondary lactase deficiency
E738Other lactose intolerance
E739Lactose intolerance, unspecified
E7400Glycogen storage disease, unspecified
E7401von Gierke disease
E7402Pompe disease
E7403Cori disease
E7404McArdle disease
E7405Lysosome-associated membrane protein 2 [LAMP2] deficiency
E7409Other glycogen storage disease
E7410Disorder of fructose metabolism, unspecified
E7411Essential fructosuria
E7412Hereditary fructose intolerance
E7419Other disorders of fructose metabolism
E7420Disorders of galactose metabolism, unspecified
E7421Galactosemia
E7429Other disorders of galactose metabolism
E7431Sucrase-isomaltase deficiency
E7439Other disorders of intestinal carbohydrate absorption
E744Disorders of pyruvate metabolism and gluconeogenesis
E74810Glucose transporter protein type 1 deficiency
E74818Other disorders of glucose transport
E74819Disorders of glucose transport, unspecified
E7489Other specified disorders of carbohydrate metabolism
E749Disorder of carbohydrate metabolism, unspecified
E7521Fabry (-Anderson) disease
E7522Gaucher disease
E75240Niemann-Pick disease type A
E75241Niemann-Pick disease type B
E75242Niemann-Pick disease type C
E75243Niemann-Pick disease type D
E75248Other Niemann-Pick disease
E75249Niemann-Pick disease, unspecified
E753Sphingolipidosis, unspecified
E755Other lipid storage disorders
E756Lipid storage disorder, unspecified
E770Defects in post-translational modification of lysosomal enzymes
E771Defects in glycoprotein degradation
E778Other disorders of glycoprotein metabolism
E779Disorder of glycoprotein metabolism, unspecified
E7800Pure hypercholesterolemia, unspecified
E7801Familial hypercholesterolemia
E781Pure hyperglyceridemia
E782Mixed hyperlipidemia
E783Hyperchylomicronemia
E7841Elevated Lipoprotein(a)
E7849Other hyperlipidemia
E785Hyperlipidemia, unspecified
E786Lipoprotein deficiency
E7870Disorder of bile acid and cholesterol metabolism, unspecified
E7879Other disorders of bile acid and cholesterol metabolism
E7881Lipoid dermatoarthritis
E7889Other lipoprotein metabolism disorders
E789Disorder of lipoprotein metabolism, unspecified
E8802Plasminogen deficiency
E8809Other disorders of plasma-protein metabolism, not elsewhere classified
E881Lipodystrophy, not elsewhere classified
E882Lipomatosis, not elsewhere classified
E88811Insulin resistance syndrome, Type A
E88818Other insulin resistance
E88819Insulin resistance, unspecified
E8889Other specified metabolic disorders
 
PDX Collection 6551
E7871Barth syndrome
E7872Smith-Lemli-Opitz syndrome
I230Hemopericardium as current complication following acute myocardial infarction
I231Atrial septal defect as current complication following acute myocardial infarction
I232Ventricular septal defect as current complication following acute myocardial infarction
I233Rupture of cardiac wall without hemopericardium as current complication following acute myocardial infarction
I236Thrombosis of atrium, auricular appendage, and ventricle as current complications following acute myocardial infarction
I237Postinfarction angina
I238Other current complications following acute myocardial infarction
I510Cardiac septal defect, acquired
P2930Pulmonary hypertension of newborn
P2938Other persistent fetal circulation
Q200Common arterial trunk
Q201Double outlet right ventricle
Q202Double outlet left ventricle
Q203Discordant ventriculoarterial connection
Q204Double inlet ventricle
Q205Discordant atrioventricular connection
Q206Isomerism of atrial appendages
Q208Other congenital malformations of cardiac chambers and connections
Q209Congenital malformation of cardiac chambers and connections, unspecified
Q210Ventricular septal defect
Q2110Atrial septal defect, unspecified
Q2111Secundum atrial septal defect
Q2112Patent foramen ovale
Q2113Coronary sinus atrial septal defect
Q2114Superior sinus venosus atrial septal defect
Q2115Inferior sinus venosus atrial septal defect
Q2116Sinus venosus atrial septal defect, unspecified
Q2119Other specified atrial septal defect
Q2120Atrioventricular septal defect, unspecified as to partial or complete
Q2121Partial atrioventricular septal defect
Q2122Transitional atrioventricular septal defect
Q2123Complete atrioventricular septal defect
Q213Tetralogy of Fallot
Q214Aortopulmonary septal defect
Q218Other congenital malformations of cardiac septa
Q219Congenital malformation of cardiac septum, unspecified
Q238Other congenital malformations of aortic and mitral valves
Q239Congenital malformation of aortic and mitral valves, unspecified
Q248Other specified congenital malformations of heart
Q249Congenital malformation of heart, unspecified
Q2730Arteriovenous malformation, site unspecified
Q274Congenital phlebectasia
Q280Arteriovenous malformation of precerebral vessels
Q281Other malformations of precerebral vessels
Q288Other specified congenital malformations of circulatory system
Q289Congenital malformation of circulatory system, unspecified
Q8711Prader-Willi syndrome
Q8719Other congenital malformation syndromes predominantly associated with short stature
Q872Congenital malformation syndromes predominantly involving limbs
Q873Congenital malformation syndromes involving early overgrowth
Q8740Marfan syndrome, unspecified
Q87410Marfan syndrome with aortic dilation
Q87418Marfan syndrome with other cardiovascular manifestations
Q8742Marfan syndrome with ocular manifestations
Q8743Marfan syndrome with skeletal manifestation
Q875Other congenital malformation syndromes with other skeletal changes
Q8781Alport syndrome
Q8782Arterial tortuosity syndrome
Q8783Bardet-Biedl syndrome
Q8784Laurence-Moon syndrome
Q8785MED13L syndrome
Q8789Other specified congenital malformation syndromes, not elsewhere classified
Q897Multiple congenital malformations, not elsewhere classified
Q898Other specified congenital malformations
Q992Fragile X chromosome
 
PDX Collection 6552
E7081Aromatic L-amino acid decarboxylase deficiency
E7089Other disorders of aromatic amino-acid metabolism
E7250Disorder of glycine metabolism, unspecified
E7251Non-ketotic hyperglycinemia
E7252Trimethylaminuria
E7253Primary hyperoxaluria
E7259Other disorders of glycine metabolism
E7281Disorders of gamma aminobutyric acid metabolism
E7289Other specified disorders of amino-acid metabolism
E729Disorder of amino-acid metabolism, unspecified
E730Congenital lactase deficiency
E731Secondary lactase deficiency
E738Other lactose intolerance
E739Lactose intolerance, unspecified
E7400Glycogen storage disease, unspecified
E7401von Gierke disease
E7402Pompe disease
E7403Cori disease
E7404McArdle disease
E7405Lysosome-associated membrane protein 2 [LAMP2] deficiency
E7409Other glycogen storage disease
E7410Disorder of fructose metabolism, unspecified
E7411Essential fructosuria
E7412Hereditary fructose intolerance
E7419Other disorders of fructose metabolism
E7420Disorders of galactose metabolism, unspecified
E7421Galactosemia
E7429Other disorders of galactose metabolism
E7431Sucrase-isomaltase deficiency
E7439Other disorders of intestinal carbohydrate absorption
E744Disorders of pyruvate metabolism and gluconeogenesis
E74810Glucose transporter protein type 1 deficiency
E74818Other disorders of glucose transport
E74819Disorders of glucose transport, unspecified
E7489Other specified disorders of carbohydrate metabolism
E749Disorder of carbohydrate metabolism, unspecified
E7521Fabry (-Anderson) disease
E7522Gaucher disease
E75240Niemann-Pick disease type A
E75241Niemann-Pick disease type B
E75242Niemann-Pick disease type C
E75243Niemann-Pick disease type D
E75248Other Niemann-Pick disease
E75249Niemann-Pick disease, unspecified
E753Sphingolipidosis, unspecified
E755Other lipid storage disorders
E756Lipid storage disorder, unspecified
E770Defects in post-translational modification of lysosomal enzymes
E771Defects in glycoprotein degradation
E778Other disorders of glycoprotein metabolism
E779Disorder of glycoprotein metabolism, unspecified
 
PDX Collection 6553
C965Multifocal and unisystemic Langerhans-cell histiocytosis
C966Unifocal Langerhans-cell histiocytosis
E71310Long chain/very long chain acyl CoA dehydrogenase deficiency
E71311Medium chain acyl CoA dehydrogenase deficiency
E71312Short chain acyl CoA dehydrogenase deficiency
E71313Glutaric aciduria type II
E71314Muscle carnitine palmitoyltransferase deficiency
E71318Other disorders of fatty-acid oxidation
E7132Disorders of ketone metabolism
E7139Other disorders of fatty-acid metabolism
E7140Disorder of carnitine metabolism, unspecified
E7141Primary carnitine deficiency
E7142Carnitine deficiency due to inborn errors of metabolism
E7143Iatrogenic carnitine deficiency
E71440Ruvalcaba-Myhre-Smith syndrome
E71448Other secondary carnitine deficiency
E71542Other group 3 peroxisomal disorders
E803Defects of catalase and peroxidase
E804Gilbert syndrome
E805Crigler-Najjar syndrome
E806Other disorders of bilirubin metabolism
E807Disorder of bilirubin metabolism, unspecified
E8840Mitochondrial metabolism disorder, unspecified
E8841MELAS syndrome
E8842MERRF syndrome
E8843Disorders of mitochondrial tRNA synthetases
E8849Other mitochondrial metabolism disorders
E88811Insulin resistance syndrome, Type A
E88818Other insulin resistance
E88819Insulin resistance, unspecified
E8889Other specified metabolic disorders
H49811Kearns-Sayre syndrome, right eye
H49812Kearns-Sayre syndrome, left eye
H49813Kearns-Sayre syndrome, bilateral
H49819Kearns-Sayre syndrome, unspecified eye
 
PDX Collection 6554
A150Tuberculosis of lung
A154Tuberculosis of intrathoracic lymph nodes
A155Tuberculosis of larynx, trachea and bronchus
A156Tuberculous pleurisy
A158Other respiratory tuberculosis
A159Respiratory tuberculosis unspecified
A179Tuberculosis of nervous system, unspecified
A1882Tuberculosis of other endocrine glands
A1884Tuberculosis of heart
A1889Tuberculosis of other sites
A212Pulmonary tularemia
A221Pulmonary anthrax
A310Pulmonary mycobacterial infection
A3701Whooping cough due to Bordetella pertussis with pneumonia
A3711Whooping cough due to Bordetella parapertussis with pneumonia
A3781Whooping cough due to other Bordetella species with pneumonia
A3791Whooping cough, unspecified species with pneumonia
A420Pulmonary actinomycosis
A430Pulmonary nocardiosis
A481Legionnaires' disease
B250Cytomegaloviral pneumonitis
B390Acute pulmonary histoplasmosis capsulati
B391Chronic pulmonary histoplasmosis capsulati
B392Pulmonary histoplasmosis capsulati, unspecified
B440Invasive pulmonary aspergillosis
B583Pulmonary toxoplasmosis
B59Pneumocystosis
B671Echinococcus granulosus infection of lung
J09X1Influenza due to identified novel influenza A virus with pneumonia
J09X2Influenza due to identified novel influenza A virus with other respiratory manifestations
J1000Influenza due to other identified influenza virus with unspecified type of pneumonia
J1001Influenza due to other identified influenza virus with the same other identified influenza virus pneumonia
J1008Influenza due to other identified influenza virus with other specified pneumonia
J101Influenza due to other identified influenza virus with other respiratory manifestations
J1100Influenza due to unidentified influenza virus with unspecified type of pneumonia
J1108Influenza due to unidentified influenza virus with specified pneumonia
J111Influenza due to unidentified influenza virus with other respiratory manifestations
J120Adenoviral pneumonia
J121Respiratory syncytial virus pneumonia
J122Parainfluenza virus pneumonia
J123Human metapneumovirus pneumonia
J1289Other viral pneumonia
J129Viral pneumonia, unspecified
J13Pneumonia due to Streptococcus pneumoniae
J14Pneumonia due to Hemophilus influenzae
J150Pneumonia due to Klebsiella pneumoniae
J151Pneumonia due to Pseudomonas
J1520Pneumonia due to staphylococcus, unspecified
J15211Pneumonia due to Methicillin susceptible Staphylococcus aureus
J15212Pneumonia due to Methicillin resistant Staphylococcus aureus
J1529Pneumonia due to other staphylococcus
J153Pneumonia due to streptococcus, group B
J154Pneumonia due to other streptococci
J155Pneumonia due to Escherichia coli
J1561Pneumonia due to Acinetobacter baumannii
J1569Pneumonia due to other Gram-negative bacteria
J157Pneumonia due to Mycoplasma pneumoniae
J158Pneumonia due to other specified bacteria
J159Unspecified bacterial pneumonia
J160Chlamydial pneumonia
J168Pneumonia due to other specified infectious organisms
J180Bronchopneumonia, unspecified organism
J181Lobar pneumonia, unspecified organism
J188Other pneumonia, unspecified organism
J189Pneumonia, unspecified organism
J22Unspecified acute lower respiratory infection
J4481Bronchiolitis obliterans and bronchiolitis obliterans syndrome
J4489Other specified chronic obstructive pulmonary disease
J449Chronic obstructive pulmonary disease, unspecified
J470Bronchiectasis with acute lower respiratory infection
J471Bronchiectasis with (acute) exacerbation
J479Bronchiectasis, uncomplicated
J4A0Restrictive allograft syndrome
J4A8Other chronic lung allograft dysfunction
J4A9Chronic lung allograft dysfunction, unspecified
J60Coalworker's pneumoconiosis
J61Pneumoconiosis due to asbestos and other mineral fibers
J620Pneumoconiosis due to talc dust
J628Pneumoconiosis due to other dust containing silica
J630Aluminosis (of lung)
J631Bauxite fibrosis (of lung)
J632Berylliosis
J633Graphite fibrosis (of lung)
J634Siderosis
J635Stannosis
J636Pneumoconiosis due to other specified inorganic dusts
J64Unspecified pneumoconiosis
J65Pneumoconiosis associated with tuberculosis
J660Byssinosis
J661Flax-dressers' disease
J662Cannabinosis
J668Airway disease due to other specific organic dusts
J670Farmer's lung
J671Bagassosis
J672Bird fancier's lung
J673Suberosis
J674Maltworker's lung
J675Mushroom-worker's lung
J676Maple-bark-stripper's lung
J677Air conditioner and humidifier lung
J678Hypersensitivity pneumonitis due to other organic dusts
J679Hypersensitivity pneumonitis due to unspecified organic dust
J680Bronchitis and pneumonitis due to chemicals, gases, fumes and vapors
J681Pulmonary edema due to chemicals, gases, fumes and vapors
J682Upper respiratory inflammation due to chemicals, gases, fumes and vapors, not elsewhere classified
J683Other acute and subacute respiratory conditions due to chemicals, gases, fumes and vapors
J684Chronic respiratory conditions due to chemicals, gases, fumes and vapors
J688Other respiratory conditions due to chemicals, gases, fumes and vapors
J689Unspecified respiratory condition due to chemicals, gases, fumes and vapors
J690Pneumonitis due to inhalation of food and vomit
J691Pneumonitis due to inhalation of oils and essences
J698Pneumonitis due to inhalation of other solids and liquids
J700Acute pulmonary manifestations due to radiation
J701Chronic and other pulmonary manifestations due to radiation
J702Acute drug-induced interstitial lung disorders
J703Chronic drug-induced interstitial lung disorders
J704Drug-induced interstitial lung disorders, unspecified
J708Respiratory conditions due to other specified external agents
J709Respiratory conditions due to unspecified external agent
J984Other disorders of lung
J988Other specified respiratory disorders
J989Respiratory disorder, unspecified
N80B1Endometriosis of pleura
N80B2Endometriosis of lung
N80B31Superficial endometriosis of diaphragm
N80B32Deep endometriosis of diaphragm
N80B39Endometriosis of diaphragm, unspecified depth
Q334Congenital bronchiectasis
R911Solitary pulmonary nodule
 
PDX Collection 6555
K560Paralytic ileus
K561Intussusception
K562Volvulus
K563Gallstone ileus
K5649Other impaction of intestine
K5650Intestinal adhesions [bands], unspecified as to partial versus complete obstruction
K5651Intestinal adhesions [bands], with partial obstruction
K5652Intestinal adhesions [bands] with complete obstruction
K56600Partial intestinal obstruction, unspecified as to cause
K56601Complete intestinal obstruction, unspecified as to cause
K56609Unspecified intestinal obstruction, unspecified as to partial versus complete obstruction
K56690Other partial intestinal obstruction
K56691Other complete intestinal obstruction
K56699Other intestinal obstruction unspecified as to partial versus complete obstruction
K567Ileus, unspecified
K634Enteroptosis
K638211Small intestinal bacterial overgrowth, hydrogen-subtype
K638212Small intestinal bacterial overgrowth, hydrogen sulfide-subtype
K638219Small intestinal bacterial overgrowth, unspecified
K63822Small intestinal fungal overgrowth
K63829Intestinal methanogen overgrowth, unspecified
K6389Other specified diseases of intestine
K639Disease of intestine, unspecified
K9130Postprocedural intestinal obstruction, unspecified as to partial versus complete
K9131Postprocedural partial intestinal obstruction
K9132Postprocedural complete intestinal obstruction



Centers for Medicare & Medicaid Services, 7500 Security Boulevard Baltimore, MD 21244
13 Oct 2023 12:52:35
CMS, code-revision=349, description-revision=1375