ICD-10-CM/PCS MS-DRG v41.0 Definitions Manual
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DRAFT
ICD-10-CM/PCS MS-DRG v41.0 Definitions Manual |
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| MDC 10 Endocrine, nutritional and metabolic diseases and disorders |
| Assignment of Diagnosis Codes |
| Page 2 of 2 |
| A187 E7204 |
| 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 |
| 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 |
| E7420 | Disorders of galactose metabolism, unspecified |
| E7421 | Galactosemia |
| E7429 | Other disorders of galactose metabolism |
| 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 |
| E75244 | Niemann-Pick disease type A/B |
| E75248 | Other Niemann-Pick disease |
| E75249 | Niemann-Pick disease, unspecified |
| E753 | Sphingolipidosis, unspecified |
| E755 | Other lipid storage disorders |
| E756 | Lipid storage disorder, unspecified |
| E7601 | Hurler's syndrome |
| E7602 | Hurler-Scheie syndrome |
| E7603 | Scheie's syndrome |
| E761 | Mucopolysaccharidosis, type II |
| E76210 | Morquio A mucopolysaccharidoses |
| E76211 | Morquio B mucopolysaccharidoses |
| E76219 | Morquio mucopolysaccharidoses, unspecified |
| E7622 | Sanfilippo mucopolysaccharidoses |
| E7629 | Other mucopolysaccharidoses |
| E763 | Mucopolysaccharidosis, unspecified |
| E768 | Other disorders of glucosaminoglycan metabolism |
| E769 | Glucosaminoglycan metabolism 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 |
| E791 | Lesch-Nyhan syndrome |
| E792 | Myoadenylate deaminase deficiency |
| E7981 | Aicardi-Goutières syndrome |
| E7982 | Hereditary xanthinuria |
| E7989 | Other specified disorders of purine and pyrimidine metabolism |
| E799 | Disorder of purine and pyrimidine metabolism, unspecified |
| E800 | Hereditary erythropoietic porphyria |
| E801 | Porphyria cutanea tarda |
| E8020 | Unspecified porphyria |
| E8021 | Acute intermittent (hepatic) porphyria |
| E8029 | Other porphyria |
| E803 | Defects of catalase and peroxidase |
| E8300 | Disorder of copper metabolism, unspecified |
| E8301 | Wilson's disease |
| E8309 | Other disorders of copper metabolism |
| E8310 | Disorder of iron metabolism, unspecified |
| E83110 | Hereditary hemochromatosis |
| E83111 | Hemochromatosis due to repeated red blood cell transfusions |
| E83118 | Other hemochromatosis |
| E83119 | Hemochromatosis, unspecified |
| E8319 | Other disorders of iron metabolism |
| E8330 | Disorder of phosphorus metabolism, unspecified |
| E8331 | Familial hypophosphatemia |
| E8332 | Hereditary vitamin D-dependent rickets (type 1) (type 2) |
| E8339 | Other disorders of phosphorus metabolism |
| E8340 | Disorders of magnesium metabolism, unspecified |
| E8341 | Hypermagnesemia |
| E8342 | Hypomagnesemia |
| E8349 | Other disorders of magnesium metabolism |
| E8350 | Unspecified disorder of calcium metabolism |
| E8351 | Hypocalcemia |
| E8352 | Hypercalcemia |
| E8359 | Other disorders of calcium metabolism |
| E8381 | Hungry bone syndrome |
| E8389 | Other disorders of mineral metabolism |
| E839 | Disorder of mineral metabolism, unspecified |
| E848 | Cystic fibrosis with other manifestations |
| E849 | Cystic fibrosis, unspecified |
| E860 | Dehydration |
| E861 | Hypovolemia |
| E869 | Volume depletion, unspecified |
| E870 | Hyperosmolality and hypernatremia |
| E871 | Hypo-osmolality and hyponatremia |
| E8720 | Acidosis, unspecified |
| E8721 | Acute metabolic acidosis |
| E8722 | Chronic metabolic acidosis |
| E8729 | Other acidosis |
| E873 | Alkalosis |
| E874 | Mixed disorder of acid-base balance |
| E875 | Hyperkalemia |
| E876 | Hypokalemia |
| E8770 | Fluid overload, unspecified |
| E8771 | Transfusion associated circulatory overload |
| E8779 | Other fluid overload |
| E878 | Other disorders of electrolyte and fluid balance, not elsewhere classified |
| E8801 | Alpha-1-antitrypsin deficiency |
| E881 | Lipodystrophy, not elsewhere classified |
| E882 | Lipomatosis, not elsewhere classified |
| E8840 | Mitochondrial metabolism disorder, unspecified |
| E8841 | MELAS syndrome |
| E8842 | MERRF syndrome |
| E8843 | Disorders of mitochondrial tRNA synthetases |
| E8849 | Other mitochondrial metabolism disorders |
| E88810 | Metabolic syndrome |
| E88811 | Insulin resistance syndrome, Type A |
| E88818 | Other insulin resistance |
| E88819 | Insulin resistance, unspecified |
| E8889 | Other specified metabolic disorders |
| E889 | Metabolic disorder, unspecified |
| E88A | Wasting disease (syndrome) due to underlying condition |
| E890 | Postprocedural hypothyroidism |
| E891 | Postprocedural hypoinsulinemia |
| E892 | Postprocedural hypoparathyroidism |
| E893 | Postprocedural hypopituitarism |
| E895 | Postprocedural testicular hypofunction |
| E896 | Postprocedural adrenocortical (-medullary) hypofunction |
| H49811 | Kearns-Sayre syndrome, right eye |
| H49812 | Kearns-Sayre syndrome, left eye |
| H49813 | Kearns-Sayre syndrome, bilateral |
| H49819 | Kearns-Sayre syndrome, unspecified eye |
| P926 | Failure to thrive in newborn |
| Q891 | Congenital malformations of adrenal gland |
| Q892 | Congenital malformations of other endocrine glands |
| R290 | Tetany |
| R620 | Delayed milestone in childhood |
| R6250 | Unspecified lack of expected normal physiological development in childhood |
| R6251 | Failure to thrive (child) |
| R6252 | Short stature (child) |
| R6259 | Other lack of expected normal physiological development in childhood |
| R627 | Adult failure to thrive |
| R630 | Anorexia |
| R631 | Polydipsia |
| R632 | Polyphagia |
| R6330 | Feeding difficulties, unspecified |
| R6331 | Pediatric feeding disorder, acute |
| R6332 | Pediatric feeding disorder, chronic |
| R6339 | Other feeding difficulties |
| R634 | Abnormal weight loss |
| R635 | Abnormal weight gain |
| R636 | Underweight |
| R638 | Other symptoms and signs concerning food and fluid intake |
| R7301 | Impaired fasting glucose |
| R7302 | Impaired glucose tolerance (oral) |
| R7303 | Prediabetes |
| R7309 | Other abnormal glucose |
| R739 | Hyperglycemia, unspecified |
| R81 | Glycosuria |
| R824 | Acetonuria |
| R946 | Abnormal results of thyroid function studies |
| R947 | Abnormal results of other endocrine function studies |
| S1110XA | Unspecified open wound of thyroid gland, initial encounter |
| S1111XA | Laceration without foreign body of thyroid gland, initial encounter |
| S1112XA | Laceration with foreign body of thyroid gland, initial encounter |
| S1113XA | Puncture wound without foreign body of thyroid gland, initial encounter |
| S1114XA | Puncture wound with foreign body of thyroid gland, initial encounter |
| S1115XA | Open bite of thyroid gland, initial encounter |
| S37812A | Contusion of adrenal gland, initial encounter |
| S37813A | Laceration of adrenal gland, initial encounter |
| S37818A | Other injury of adrenal gland, initial encounter |
| S37819A | Unspecified injury of adrenal gland, initial encounter |
| Z6841 | Body mass index [BMI] 40.0-44.9, adult |
| Z6842 | Body mass index [BMI] 45.0-49.9, adult |
| Z6843 | Body mass index [BMI] 50.0-59.9, adult |
| Z6844 | Body mass index [BMI] 60.0-69.9, adult |
| Z6845 | Body mass index [BMI] 70 or greater, adult |
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Centers for Medicare & Medicaid Services, 7500 Security Boulevard Baltimore, MD 21244 01 Mar 2023 06:12:40 CMS, code-revision=344, description-revision=1357 |