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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 1261 of 1375 |
PDX Collection 6643 | |
C880 | Waldenstrom macroglobulinemia |
D472 | Monoclonal gammopathy |
D890 | Polyclonal hypergammaglobulinemia |
D891 | Cryoglobulinemia |
E700 | Classical phenylketonuria |
E701 | Other hyperphenylalaninemias |
E7020 | Disorder of tyrosine metabolism, unspecified |
E7021 | Tyrosinemia |
E7029 | Other disorders of tyrosine metabolism |
E7030 | Albinism, unspecified |
E70310 | X-linked ocular albinism |
E70311 | Autosomal recessive ocular albinism |
E70318 | Other ocular albinism |
E70319 | Ocular albinism, unspecified |
E70320 | Tyrosinase negative oculocutaneous albinism |
E70321 | Tyrosinase positive oculocutaneous albinism |
E70328 | Other oculocutaneous albinism |
E70329 | Oculocutaneous albinism, unspecified |
E70330 | Chediak-Higashi syndrome |
E70331 | Hermansky-Pudlak syndrome |
E70338 | Other albinism with hematologic abnormality |
E70339 | Albinism with hematologic abnormality, unspecified |
E7039 | Other specified albinism |
E7040 | Disorders of histidine metabolism, unspecified |
E7041 | Histidinemia |
E7049 | Other disorders of histidine metabolism |
E705 | Disorders of tryptophan metabolism |
E7081 | Aromatic L-amino acid decarboxylase deficiency |
E7089 | Other disorders of aromatic amino-acid metabolism |
E709 | Disorder of aromatic amino-acid metabolism, unspecified |
E710 | Maple-syrup-urine disease |
E71110 | Isovaleric acidemia |
E71111 | 3-methylglutaconic aciduria |
E71118 | Other branched-chain organic acidurias |
E71120 | Methylmalonic acidemia |
E71121 | Propionic acidemia |
E71128 | Other disorders of propionate metabolism |
E7119 | Other disorders of branched-chain amino-acid metabolism |
E712 | Disorder of branched-chain amino-acid metabolism, unspecified |
E7130 | Disorder of fatty-acid metabolism, unspecified |
E7200 | Disorders of amino-acid transport, unspecified |
E7201 | Cystinuria |
E7202 | Hartnup's disease |
E7204 | Cystinosis |
E7209 | Other disorders of amino-acid transport |
E7210 | Disorders of sulfur-bearing amino-acid metabolism, unspecified |
E7211 | Homocystinuria |
E7212 | Methylenetetrahydrofolate reductase deficiency |
E7219 | Other disorders of sulfur-bearing amino-acid metabolism |
E7220 | Disorder of urea cycle metabolism, unspecified |
E7221 | Argininemia |
E7222 | Arginosuccinic aciduria |
E7223 | Citrullinemia |
E7229 | Other disorders of urea cycle metabolism |
E723 | Disorders of lysine and hydroxylysine metabolism |
E724 | Disorders of ornithine metabolism |
E7250 | Disorder of glycine metabolism, unspecified |
E7251 | Non-ketotic hyperglycinemia |
E7252 | Trimethylaminuria |
E7253 | Primary hyperoxaluria |
E7259 | Other disorders of glycine metabolism |
E7281 | Disorders of gamma aminobutyric acid metabolism |
E7289 | Other specified disorders of amino-acid metabolism |
E729 | Disorder of amino-acid metabolism, unspecified |
E730 | Congenital lactase deficiency |
E731 | Secondary lactase deficiency |
E738 | Other lactose intolerance |
E739 | Lactose intolerance, unspecified |
E7400 | Glycogen storage disease, unspecified |
E7401 | von Gierke disease |
E7402 | Pompe disease |
E7403 | Cori disease |
E7404 | McArdle disease |
E7405 | Lysosome-associated membrane protein 2 [LAMP2] deficiency |
E7409 | Other glycogen storage disease |
E7410 | Disorder of fructose metabolism, unspecified |
E7411 | Essential fructosuria |
E7412 | Hereditary fructose intolerance |
E7419 | Other disorders of fructose metabolism |
E7420 | Disorders of galactose metabolism, unspecified |
E7421 | Galactosemia |
E7429 | Other disorders of galactose metabolism |
E7431 | Sucrase-isomaltase deficiency |
E7439 | Other disorders of intestinal carbohydrate absorption |
E744 | Disorders of pyruvate metabolism and gluconeogenesis |
E74810 | Glucose transporter protein type 1 deficiency |
E74818 | Other disorders of glucose transport |
E74819 | Disorders of glucose transport, unspecified |
E7489 | Other specified disorders of carbohydrate metabolism |
E749 | Disorder of carbohydrate metabolism, unspecified |
E7521 | Fabry (-Anderson) disease |
E7522 | Gaucher disease |
E75240 | Niemann-Pick disease type A |
E75241 | Niemann-Pick disease type B |
E75242 | Niemann-Pick disease type C |
E75243 | Niemann-Pick disease type D |
E75248 | Other Niemann-Pick disease |
E75249 | Niemann-Pick disease, unspecified |
E753 | Sphingolipidosis, unspecified |
E755 | Other lipid storage disorders |
E756 | Lipid storage disorder, unspecified |
E770 | Defects in post-translational modification of lysosomal enzymes |
E771 | Defects in glycoprotein degradation |
E778 | Other disorders of glycoprotein metabolism |
E779 | Disorder of glycoprotein metabolism, unspecified |
E7800 | Pure hypercholesterolemia, unspecified |
E7801 | Familial hypercholesterolemia |
E781 | Pure hyperglyceridemia |
E782 | Mixed hyperlipidemia |
E783 | Hyperchylomicronemia |
E7841 | Elevated Lipoprotein(a) |
E7849 | Other hyperlipidemia |
E785 | Hyperlipidemia, unspecified |
E786 | Lipoprotein deficiency |
E7870 | Disorder of bile acid and cholesterol metabolism, unspecified |
E7879 | Other disorders of bile acid and cholesterol metabolism |
E7881 | Lipoid dermatoarthritis |
E7889 | Other lipoprotein metabolism disorders |
E789 | Disorder of lipoprotein metabolism, unspecified |
E8802 | Plasminogen deficiency |
E8809 | Other disorders of plasma-protein metabolism, not elsewhere classified |
E881 | Lipodystrophy, not elsewhere classified |
E882 | Lipomatosis, not elsewhere classified |
E8889 | Other specified metabolic disorders |
PDX Collection 6644 | |
C880 | Waldenstrom macroglobulinemia |
D472 | Monoclonal gammopathy |
D890 | Polyclonal hypergammaglobulinemia |
D891 | Cryoglobulinemia |
E700 | Classical phenylketonuria |
E701 | Other hyperphenylalaninemias |
E7020 | Disorder of tyrosine metabolism, unspecified |
E7021 | Tyrosinemia |
E7029 | Other disorders of tyrosine metabolism |
E7030 | Albinism, unspecified |
E70310 | X-linked ocular albinism |
E70311 | Autosomal recessive ocular albinism |
E70318 | Other ocular albinism |
E70319 | Ocular albinism, unspecified |
E70320 | Tyrosinase negative oculocutaneous albinism |
E70321 | Tyrosinase positive oculocutaneous albinism |
E70328 | Other oculocutaneous albinism |
E70329 | Oculocutaneous albinism, unspecified |
E70330 | Chediak-Higashi syndrome |
E70331 | Hermansky-Pudlak syndrome |
E70338 | Other albinism with hematologic abnormality |
E70339 | Albinism with hematologic abnormality, unspecified |
E7039 | Other specified albinism |
E7040 | Disorders of histidine metabolism, unspecified |
E7041 | Histidinemia |
E7049 | Other disorders of histidine metabolism |
E705 | Disorders of tryptophan metabolism |
E7081 | Aromatic L-amino acid decarboxylase deficiency |
E7089 | Other disorders of aromatic amino-acid metabolism |
E709 | Disorder of aromatic amino-acid metabolism, unspecified |
E710 | Maple-syrup-urine disease |
E71110 | Isovaleric acidemia |
E71111 | 3-methylglutaconic aciduria |
E71118 | Other branched-chain organic acidurias |
E71120 | Methylmalonic acidemia |
E71121 | Propionic acidemia |
E71128 | Other disorders of propionate metabolism |
E7119 | Other disorders of branched-chain amino-acid metabolism |
E712 | Disorder of branched-chain amino-acid metabolism, unspecified |
E7130 | Disorder of fatty-acid metabolism, unspecified |
E7200 | Disorders of amino-acid transport, unspecified |
E7201 | Cystinuria |
E7202 | Hartnup's disease |
E7204 | Cystinosis |
E7209 | Other disorders of amino-acid transport |
E7210 | Disorders of sulfur-bearing amino-acid metabolism, unspecified |
E7211 | Homocystinuria |
E7212 | Methylenetetrahydrofolate reductase deficiency |
E7219 | Other disorders of sulfur-bearing amino-acid metabolism |
E7220 | Disorder of urea cycle metabolism, unspecified |
E7221 | Argininemia |
E7222 | Arginosuccinic aciduria |
E7223 | Citrullinemia |
E7229 | Other disorders of urea cycle metabolism |
E723 | Disorders of lysine and hydroxylysine metabolism |
E724 | Disorders of ornithine metabolism |
E7250 | Disorder of glycine metabolism, unspecified |
E7251 | Non-ketotic hyperglycinemia |
E7252 | Trimethylaminuria |
E7253 | Primary hyperoxaluria |
E7259 | Other disorders of glycine metabolism |
E7281 | Disorders of gamma aminobutyric acid metabolism |
E7289 | Other specified disorders of amino-acid metabolism |
E729 | Disorder of amino-acid metabolism, unspecified |
E730 | Congenital lactase deficiency |
E731 | Secondary lactase deficiency |
E738 | Other lactose intolerance |
E739 | Lactose intolerance, unspecified |
E7400 | Glycogen storage disease, unspecified |
E7401 | von Gierke disease |
E7402 | Pompe disease |
E7403 | Cori disease |
E7404 | McArdle disease |
E7405 | Lysosome-associated membrane protein 2 [LAMP2] deficiency |
E7409 | Other glycogen storage disease |
E7410 | Disorder of fructose metabolism, unspecified |
E7411 | Essential fructosuria |
E7412 | Hereditary fructose intolerance |
E7419 | Other disorders of fructose metabolism |
E7420 | Disorders of galactose metabolism, unspecified |
E7421 | Galactosemia |
E7429 | Other disorders of galactose metabolism |
E7431 | Sucrase-isomaltase deficiency |
E7439 | Other disorders of intestinal carbohydrate absorption |
E744 | Disorders of pyruvate metabolism and gluconeogenesis |
E74810 | Glucose transporter protein type 1 deficiency |
E74818 | Other disorders of glucose transport |
E74819 | Disorders of glucose transport, unspecified |
E7489 | Other specified disorders of carbohydrate metabolism |
E749 | Disorder of carbohydrate metabolism, unspecified |
E7521 | Fabry (-Anderson) disease |
E7522 | Gaucher disease |
E75240 | Niemann-Pick disease type A |
E75241 | Niemann-Pick disease type B |
E75242 | Niemann-Pick disease type C |
E75243 | Niemann-Pick disease type D |
E75248 | Other Niemann-Pick disease |
E75249 | Niemann-Pick disease, unspecified |
E753 | Sphingolipidosis, unspecified |
E755 | Other lipid storage disorders |
E756 | Lipid storage disorder, unspecified |
E770 | Defects in post-translational modification of lysosomal enzymes |
E771 | Defects in glycoprotein degradation |
E778 | Other disorders of glycoprotein metabolism |
E779 | Disorder of glycoprotein metabolism, unspecified |
E7800 | Pure hypercholesterolemia, unspecified |
E7801 | Familial hypercholesterolemia |
E781 | Pure hyperglyceridemia |
E782 | Mixed hyperlipidemia |
E783 | Hyperchylomicronemia |
E7841 | Elevated Lipoprotein(a) |
E7849 | Other hyperlipidemia |
E785 | Hyperlipidemia, unspecified |
E786 | Lipoprotein deficiency |
E7870 | Disorder of bile acid and cholesterol metabolism, unspecified |
E7879 | Other disorders of bile acid and cholesterol metabolism |
E7881 | Lipoid dermatoarthritis |
E7889 | Other lipoprotein metabolism disorders |
E789 | Disorder of lipoprotein metabolism, unspecified |
E8802 | Plasminogen deficiency |
E8809 | Other disorders of plasma-protein metabolism, not elsewhere classified |
E881 | Lipodystrophy, not elsewhere classified |
E882 | Lipomatosis, not elsewhere classified |
E88811 | Insulin resistance syndrome, Type A |
E88818 | Other insulin resistance |
E88819 | Insulin resistance, unspecified |
E8889 | Other specified metabolic disorders |
PDX Collection 6645 | |
C880 | Waldenstrom macroglobulinemia |
D472 | Monoclonal gammopathy |
D890 | Polyclonal hypergammaglobulinemia |
D891 | Cryoglobulinemia |
E700 | Classical phenylketonuria |
E701 | Other hyperphenylalaninemias |
E7020 | Disorder of tyrosine metabolism, unspecified |
E7021 | Tyrosinemia |
E7029 | Other disorders of tyrosine metabolism |
E7030 | Albinism, unspecified |
E70310 | X-linked ocular albinism |
E70311 | Autosomal recessive ocular albinism |
E70318 | Other ocular albinism |
E70319 | Ocular albinism, unspecified |
E70320 | Tyrosinase negative oculocutaneous albinism |
E70321 | Tyrosinase positive oculocutaneous albinism |
E70328 | Other oculocutaneous albinism |
E70329 | Oculocutaneous albinism, unspecified |
E70330 | Chediak-Higashi syndrome |
E70331 | Hermansky-Pudlak syndrome |
E70338 | Other albinism with hematologic abnormality |
E70339 | Albinism with hematologic abnormality, unspecified |
E7039 | Other specified albinism |
E7040 | Disorders of histidine metabolism, unspecified |
E7041 | Histidinemia |
E7049 | Other disorders of histidine metabolism |
E705 | Disorders of tryptophan metabolism |
E7081 | Aromatic L-amino acid decarboxylase deficiency |
E7089 | Other disorders of aromatic amino-acid metabolism |
E709 | Disorder of aromatic amino-acid metabolism, unspecified |
E710 | Maple-syrup-urine disease |
E71110 | Isovaleric acidemia |
E71111 | 3-methylglutaconic aciduria |
E71118 | Other branched-chain organic acidurias |
E71120 | Methylmalonic acidemia |
E71121 | Propionic acidemia |
E71128 | Other disorders of propionate metabolism |
E7119 | Other disorders of branched-chain amino-acid metabolism |
E712 | Disorder of branched-chain amino-acid metabolism, unspecified |
E7130 | Disorder of fatty-acid metabolism, unspecified |
E7200 | Disorders of amino-acid transport, unspecified |
E7201 | Cystinuria |
E7202 | Hartnup's disease |
E7204 | Cystinosis |
E7209 | Other disorders of amino-acid transport |
E7210 | Disorders of sulfur-bearing amino-acid metabolism, unspecified |
E7211 | Homocystinuria |
E7212 | Methylenetetrahydrofolate reductase deficiency |
E7219 | Other disorders of sulfur-bearing amino-acid metabolism |
E7220 | Disorder of urea cycle metabolism, unspecified |
E7221 | Argininemia |
E7222 | Arginosuccinic aciduria |
E7223 | Citrullinemia |
E7229 | Other disorders of urea cycle metabolism |
E723 | Disorders of lysine and hydroxylysine metabolism |
E724 | Disorders of ornithine metabolism |
E7250 | Disorder of glycine metabolism, unspecified |
E7251 | Non-ketotic hyperglycinemia |
E7252 | Trimethylaminuria |
E7253 | Primary hyperoxaluria |
E7259 | Other disorders of glycine metabolism |
E7281 | Disorders of gamma aminobutyric acid metabolism |
E7289 | Other specified disorders of amino-acid metabolism |
E729 | Disorder of amino-acid metabolism, unspecified |
E730 | Congenital lactase deficiency |
E731 | Secondary lactase deficiency |
E738 | Other lactose intolerance |
E739 | Lactose intolerance, unspecified |
E7400 | Glycogen storage disease, unspecified |
E7401 | von Gierke disease |
E7402 | Pompe disease |
E7403 | Cori disease |
E7404 | McArdle disease |
E7405 | Lysosome-associated membrane protein 2 [LAMP2] deficiency |
E7409 | Other glycogen storage disease |
E7410 | Disorder of fructose metabolism, unspecified |
E7411 | Essential fructosuria |
E7412 | Hereditary fructose intolerance |
E7419 | Other disorders of fructose metabolism |
E7420 | Disorders of galactose metabolism, unspecified |
E7421 | Galactosemia |
E7429 | Other disorders of galactose metabolism |
E7431 | Sucrase-isomaltase deficiency |
E7439 | Other disorders of intestinal carbohydrate absorption |
E744 | Disorders of pyruvate metabolism and gluconeogenesis |
E74810 | Glucose transporter protein type 1 deficiency |
E74818 | Other disorders of glucose transport |
E74819 | Disorders of glucose transport, unspecified |
E7489 | Other specified disorders of carbohydrate metabolism |
E749 | Disorder of carbohydrate metabolism, unspecified |
E7521 | Fabry (-Anderson) disease |
E7522 | Gaucher disease |
E75240 | Niemann-Pick disease type A |
E75241 | Niemann-Pick disease type B |
E75242 | Niemann-Pick disease type C |
E75243 | Niemann-Pick disease type D |
E75248 | Other Niemann-Pick disease |
E75249 | Niemann-Pick disease, unspecified |
E753 | Sphingolipidosis, unspecified |
E755 | Other lipid storage disorders |
E756 | Lipid storage disorder, unspecified |
E770 | Defects in post-translational modification of lysosomal enzymes |
E771 | Defects in glycoprotein degradation |
E778 | Other disorders of glycoprotein metabolism |
E779 | Disorder of glycoprotein metabolism, unspecified |
E7800 | Pure hypercholesterolemia, unspecified |
E7801 | Familial hypercholesterolemia |
E781 | Pure hyperglyceridemia |
E782 | Mixed hyperlipidemia |
E783 | Hyperchylomicronemia |
E7841 | Elevated Lipoprotein(a) |
E7849 | Other hyperlipidemia |
E785 | Hyperlipidemia, unspecified |
E786 | Lipoprotein deficiency |
E7870 | Disorder of bile acid and cholesterol metabolism, unspecified |
E7879 | Other disorders of bile acid and cholesterol metabolism |
E7881 | Lipoid dermatoarthritis |
E7889 | Other lipoprotein metabolism disorders |
E789 | Disorder of lipoprotein metabolism, unspecified |
E8802 | Plasminogen deficiency |
E8809 | Other disorders of plasma-protein metabolism, not elsewhere classified |
E881 | Lipodystrophy, not elsewhere classified |
E882 | Lipomatosis, not elsewhere classified |
E88811 | Insulin resistance syndrome, Type A |
E88818 | Other insulin resistance |
E88819 | Insulin resistance, unspecified |
E8889 | Other specified metabolic disorders |
PDX Collection 6646 | |
C880 | Waldenstrom macroglobulinemia |
D472 | Monoclonal gammopathy |
D890 | Polyclonal hypergammaglobulinemia |
D891 | Cryoglobulinemia |
E700 | Classical phenylketonuria |
E701 | Other hyperphenylalaninemias |
E7020 | Disorder of tyrosine metabolism, unspecified |
E7021 | Tyrosinemia |
E7029 | Other disorders of tyrosine metabolism |
E7030 | Albinism, unspecified |
E70310 | X-linked ocular albinism |
E70311 | Autosomal recessive ocular albinism |
E70318 | Other ocular albinism |
E70319 | Ocular albinism, unspecified |
E70320 | Tyrosinase negative oculocutaneous albinism |
E70321 | Tyrosinase positive oculocutaneous albinism |
E70328 | Other oculocutaneous albinism |
E70329 | Oculocutaneous albinism, unspecified |
E70330 | Chediak-Higashi syndrome |
E70331 | Hermansky-Pudlak syndrome |
E70338 | Other albinism with hematologic abnormality |
E70339 | Albinism with hematologic abnormality, unspecified |
E7039 | Other specified albinism |
Centers for Medicare & Medicaid Services, 7500 Security Boulevard Baltimore, MD 21244 01 Mar 2023 06:12:40 CMS, code-revision=344, description-revision=1357 |