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 1246 of 1324
PDX Collection 6786 (continued)
G40804Other epilepsy, intractable, without status epilepticus
G40811Lennox-Gastaut syndrome, not intractable, with status epilepticus
G40812Lennox-Gastaut syndrome, not intractable, without status epilepticus
G40813Lennox-Gastaut syndrome, intractable, with status epilepticus
G40814Lennox-Gastaut syndrome, intractable, without status epilepticus
G40821Epileptic spasms, not intractable, with status epilepticus
G40822Epileptic spasms, not intractable, without status epilepticus
G40823Epileptic spasms, intractable, with status epilepticus
G40824Epileptic spasms, intractable, without status epilepticus
G40833Dravet syndrome, intractable, with status epilepticus
G40834Dravet syndrome, intractable, without status epilepticus
G4089Other seizures
G40901Epilepsy, unspecified, not intractable, with status epilepticus
G40909Epilepsy, unspecified, not intractable, without status epilepticus
G40911Epilepsy, unspecified, intractable, with status epilepticus
G40919Epilepsy, unspecified, intractable, without status epilepticus
G40A01Absence epileptic syndrome, not intractable, with status epilepticus
G40A09Absence epileptic syndrome, not intractable, without status epilepticus
G40A11Absence epileptic syndrome, intractable, with status epilepticus
G40A19Absence epileptic syndrome, intractable, without status epilepticus
G40B01Juvenile myoclonic epilepsy, not intractable, with status epilepticus
G40B09Juvenile myoclonic epilepsy, not intractable, without status epilepticus
G40B11Juvenile myoclonic epilepsy, intractable, with status epilepticus
G40B19Juvenile myoclonic epilepsy, intractable, without status epilepticus
G40C01Lafora progressive myoclonus epilepsy, not intractable, with status epilepticus
G40C09Lafora progressive myoclonus epilepsy, not intractable, without status epilepticus
G40C11Lafora progressive myoclonus epilepsy, intractable, with status epilepticus
G40C19Lafora progressive myoclonus epilepsy, intractable, without status epilepticus
G9340Encephalopathy, unspecified
G9341Metabolic encephalopathy
G9342Megaloencephalic leukoencephalopathy with subcortical cysts
G9343Leukoencephalopathy with calcifications and cysts
G9344Adult-onset leukodystrophy with axonal spheroids
G9349Other encephalopathy
G939Disorder of brain, unspecified
G969Disorder of central nervous system, unspecified
G980Neurogenic arthritis, not elsewhere classified
G988Other disorders of nervous system
I6783Posterior reversible encephalopathy syndrome
R561Post traumatic seizures
 
PDX Collection 6787
E0940Drug or chemical induced diabetes mellitus with neurological complications with diabetic neuropathy, unspecified
E0941Drug or chemical induced diabetes mellitus with neurological complications with diabetic mononeuropathy
E0942Drug or chemical induced diabetes mellitus with neurological complications with diabetic polyneuropathy
E0943Drug or chemical induced diabetes mellitus with neurological complications with diabetic autonomic (poly)neuropathy
E0944Drug or chemical induced diabetes mellitus with neurological complications with diabetic amyotrophy
E0949Drug or chemical induced diabetes mellitus with neurological complications with other diabetic neurological complication
E1040Type 1 diabetes mellitus with diabetic neuropathy, unspecified
E1041Type 1 diabetes mellitus with diabetic mononeuropathy
E1042Type 1 diabetes mellitus with diabetic polyneuropathy
E1043Type 1 diabetes mellitus with diabetic autonomic (poly)neuropathy
E1044Type 1 diabetes mellitus with diabetic amyotrophy
E1049Type 1 diabetes mellitus with other diabetic neurological complication
E1140Type 2 diabetes mellitus with diabetic neuropathy, unspecified
E1141Type 2 diabetes mellitus with diabetic mononeuropathy
E1142Type 2 diabetes mellitus with diabetic polyneuropathy
E1143Type 2 diabetes mellitus with diabetic autonomic (poly)neuropathy
E1144Type 2 diabetes mellitus with diabetic amyotrophy
E1149Type 2 diabetes mellitus with other diabetic neurological complication
E1340Other specified diabetes mellitus with diabetic neuropathy, unspecified
E1341Other specified diabetes mellitus with diabetic mononeuropathy
E1342Other specified diabetes mellitus with diabetic polyneuropathy
E1343Other specified diabetes mellitus with diabetic autonomic (poly)neuropathy
E1344Other specified diabetes mellitus with diabetic amyotrophy
E1349Other specified diabetes mellitus with other diabetic neurological complication
G40001Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, not intractable, with status epilepticus
G40009Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, not intractable, without status epilepticus
G40011Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, intractable, with status epilepticus
G40019Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, intractable, without status epilepticus
G40101Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, not intractable, with status epilepticus
G40109Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, not intractable, without status epilepticus
G40111Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, intractable, with status epilepticus
G40119Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, intractable, without status epilepticus
G40201Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, not intractable, with status epilepticus
G40209Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, not intractable, without status epilepticus
G40211Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, intractable, with status epilepticus
G40219Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, intractable, without status epilepticus
G40301Generalized idiopathic epilepsy and epileptic syndromes, not intractable, with status epilepticus
G40309Generalized idiopathic epilepsy and epileptic syndromes, not intractable, without status epilepticus
G40311Generalized idiopathic epilepsy and epileptic syndromes, intractable, with status epilepticus
G40319Generalized idiopathic epilepsy and epileptic syndromes, intractable, without status epilepticus
G40401Other generalized epilepsy and epileptic syndromes, not intractable, with status epilepticus
G40409Other generalized epilepsy and epileptic syndromes, not intractable, without status epilepticus
G40411Other generalized epilepsy and epileptic syndromes, intractable, with status epilepticus
G40419Other generalized epilepsy and epileptic syndromes, intractable, without status epilepticus
G4042Cyclin-Dependent Kinase-Like 5 Deficiency Disorder
G40501Epileptic seizures related to external causes, not intractable, with status epilepticus
G40509Epileptic seizures related to external causes, not intractable, without status epilepticus
G40801Other epilepsy, not intractable, with status epilepticus
G40802Other epilepsy, not intractable, without status epilepticus
G40803Other epilepsy, intractable, with status epilepticus
G40804Other epilepsy, intractable, without status epilepticus
G40811Lennox-Gastaut syndrome, not intractable, with status epilepticus
G40812Lennox-Gastaut syndrome, not intractable, without status epilepticus
G40813Lennox-Gastaut syndrome, intractable, with status epilepticus
G40814Lennox-Gastaut syndrome, intractable, without status epilepticus
G40821Epileptic spasms, not intractable, with status epilepticus
G40822Epileptic spasms, not intractable, without status epilepticus
G40823Epileptic spasms, intractable, with status epilepticus
G40824Epileptic spasms, intractable, without status epilepticus
G40833Dravet syndrome, intractable, with status epilepticus
G40834Dravet syndrome, intractable, without status epilepticus
G4089Other seizures
G40901Epilepsy, unspecified, not intractable, with status epilepticus
G40909Epilepsy, unspecified, not intractable, without status epilepticus
G40911Epilepsy, unspecified, intractable, with status epilepticus
G40919Epilepsy, unspecified, intractable, without status epilepticus
G40A01Absence epileptic syndrome, not intractable, with status epilepticus
G40A09Absence epileptic syndrome, not intractable, without status epilepticus
G40A11Absence epileptic syndrome, intractable, with status epilepticus
G40A19Absence epileptic syndrome, intractable, without status epilepticus
G40B01Juvenile myoclonic epilepsy, not intractable, with status epilepticus
G40B09Juvenile myoclonic epilepsy, not intractable, without status epilepticus
G40B11Juvenile myoclonic epilepsy, intractable, with status epilepticus
G40B19Juvenile myoclonic epilepsy, intractable, without status epilepticus
G40C01Lafora progressive myoclonus epilepsy, not intractable, with status epilepticus
G40C09Lafora progressive myoclonus epilepsy, not intractable, without status epilepticus
G40C11Lafora progressive myoclonus epilepsy, intractable, with status epilepticus
G40C19Lafora progressive myoclonus epilepsy, intractable, without status epilepticus
G9381Temporal sclerosis
G9389Other specified disorders of brain
G939Disorder of brain, unspecified
G969Disorder of central nervous system, unspecified
G980Neurogenic arthritis, not elsewhere classified
G988Other disorders of nervous system
R561Post traumatic seizures
 
PDX Collection 6788
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 6789
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 6790
I200Unstable angina
I201Angina pectoris with documented spasm
I202Refractory angina pectoris
I2081Angina pectoris with coronary microvascular dysfunction
I2089Other forms of angina pectoris
I209Angina pectoris, unspecified
I2101ST elevation (STEMI) myocardial infarction involving left main coronary artery
I2102ST elevation (STEMI) myocardial infarction involving left anterior descending coronary artery
I2109ST elevation (STEMI) myocardial infarction involving other coronary artery of anterior wall
I2111ST elevation (STEMI) myocardial infarction involving right coronary artery
I2119ST elevation (STEMI) myocardial infarction involving other coronary artery of inferior wall
I2121ST elevation (STEMI) myocardial infarction involving left circumflex coronary artery
I2129ST elevation (STEMI) myocardial infarction involving other sites
I213ST elevation (STEMI) myocardial infarction of unspecified site
I214Non-ST elevation (NSTEMI) myocardial infarction
I219Acute myocardial infarction, unspecified
I21A1Myocardial infarction type 2
I21A9Other myocardial infarction type
I21BMyocardial infarction with coronary microvascular dysfunction
I220Subsequent ST elevation (STEMI) myocardial infarction of anterior wall
I221Subsequent ST elevation (STEMI) myocardial infarction of inferior wall



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