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 1197 of 1324
PDX Collection 6542 (continued)
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 6543
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 6544
Q440Agenesis, aplasia and hypoplasia of gallbladder
Q441Other congenital malformations of gallbladder
Q442Atresia of bile ducts
Q443Congenital stenosis and stricture of bile ducts
Q444Choledochal cyst
Q445Other congenital malformations of bile ducts
Q446Cystic disease of liver
Q4470Other congenital malformation of liver, unspecified
Q4471Alagille syndrome
Q4479Other congenital malformations of liver
 
PDX Collection 6545
C880Waldenstrom macroglobulinemia
D472Monoclonal gammopathy
D890Polyclonal hypergammaglobulinemia
D891Cryoglobulinemia
E700Classical phenylketonuria
E701Other hyperphenylalaninemias
E7020Disorder of tyrosine metabolism, unspecified
E7021Tyrosinemia
E7029Other disorders of tyrosine metabolism
E7030Albinism, unspecified
E70310X-linked ocular albinism
E70311Autosomal recessive ocular albinism
E70318Other ocular albinism
E70319Ocular albinism, unspecified
E70320Tyrosinase negative oculocutaneous albinism
E70321Tyrosinase positive oculocutaneous albinism
E70328Other oculocutaneous albinism
E70329Oculocutaneous albinism, unspecified
E70330Chediak-Higashi syndrome
E70331Hermansky-Pudlak syndrome
E70338Other albinism with hematologic abnormality
E70339Albinism with hematologic abnormality, unspecified
E7039Other specified albinism
E7040Disorders of histidine metabolism, unspecified
E7041Histidinemia
E7049Other disorders of histidine metabolism
E705Disorders of tryptophan metabolism
E7081Aromatic L-amino acid decarboxylase deficiency
E7089Other disorders of aromatic amino-acid metabolism
E709Disorder of aromatic amino-acid metabolism, unspecified
E710Maple-syrup-urine disease
E71110Isovaleric acidemia
E711113-methylglutaconic aciduria
E71118Other branched-chain organic acidurias
E71120Methylmalonic acidemia
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 6546
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
E71548Other 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 6547
M800AXAAge-related osteoporosis with current pathological fracture, other site, initial encounter for fracture
M800AXKAge-related osteoporosis with current pathological fracture, other site, subsequent encounter for fracture with nonunion
M800AXPAge-related osteoporosis with current pathological fracture, other site, subsequent encounter for fracture with malunion
M808AXAOther osteoporosis with current pathological fracture, other site, initial encounter for fracture
M808AXKOther osteoporosis with current pathological fracture, other site, subsequent encounter for fracture with nonunion
M808AXPOther osteoporosis with current pathological fracture, other site, subsequent encounter for fracture with malunion
M808B2KOther osteoporosis with current pathological fracture, left pelvis, subsequent encounter for fracture with nonunion
 
PDX Collection 6548
Q440Agenesis, aplasia and hypoplasia of gallbladder
Q441Other congenital malformations of gallbladder
Q442Atresia of bile ducts
Q443Congenital stenosis and stricture of bile ducts
Q444Choledochal cyst
Q445Other congenital malformations of bile ducts
Q446Cystic disease of liver
Q4470Other congenital malformation of liver, unspecified
Q4471Alagille syndrome
Q4479Other congenital malformations of liver
 
PDX Collection 6549
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 6550
C880Waldenstrom macroglobulinemia
D472Monoclonal gammopathy
D890Polyclonal hypergammaglobulinemia
D891Cryoglobulinemia
E700Classical phenylketonuria
E701Other hyperphenylalaninemias
E7020Disorder of tyrosine metabolism, unspecified
E7021Tyrosinemia
E7029Other disorders of tyrosine metabolism
E7030Albinism, unspecified
E70310X-linked ocular albinism
E70311Autosomal recessive ocular albinism
E70318Other ocular albinism
E70319Ocular albinism, unspecified
E70320Tyrosinase negative oculocutaneous albinism
E70321Tyrosinase positive oculocutaneous albinism
E70328Other oculocutaneous albinism
E70329Oculocutaneous albinism, unspecified
E70330Chediak-Higashi syndrome
E70331Hermansky-Pudlak syndrome
E70338Other albinism with hematologic abnormality
E70339Albinism with hematologic abnormality, unspecified
E7039Other specified albinism
E7040Disorders of histidine metabolism, unspecified
E7041Histidinemia
E7049Other disorders of histidine metabolism
E705Disorders of tryptophan metabolism
E7081Aromatic L-amino acid decarboxylase deficiency
E7089Other disorders of aromatic amino-acid metabolism
E709Disorder of aromatic amino-acid metabolism, unspecified
E710Maple-syrup-urine disease
E71110Isovaleric acidemia
E711113-methylglutaconic aciduria
E71118Other branched-chain organic acidurias
E71120Methylmalonic acidemia



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