| PDX Collection 0529:77 codes |
| E3601 | Intraoperative hemorrhage and hematoma of an endocrine system organ or structure complicating an endocrine system procedure |
| E3602 | Intraoperative hemorrhage and hematoma of an endocrine system organ or structure complicating other procedure |
| E368 | Other intraoperative complications of endocrine system |
| E89810 | Postprocedural hemorrhage and hematoma of an endocrine system organ or structure following an endocrine system procedure |
| E89811 | Postprocedural hemorrhage and hematoma of an endocrine system organ or structure following other procedure |
| E8989 | Other postprocedural endocrine and metabolic complications and disorders |
| H95811 | Postprocedural stenosis of right external ear canal |
| H95812 | Postprocedural stenosis of left external ear canal |
| H95813 | Postprocedural stenosis of external ear canal, bilateral |
| H95819 | Postprocedural stenosis of unspecified external ear canal |
| H9588 | Other intraoperative complications and disorders of the ear and mastoid process, not elsewhere classified |
| H9589 | Other postprocedural complications and disorders of the ear and mastoid process, not elsewhere classified |
| I8501 | Esophageal varices with bleeding |
| I8511 | Secondary esophageal varices with bleeding |
| I973 | Postprocedural hypertension |
| K219 | Gastro-esophageal reflux disease without esophagitis |
| K228 | Other specified diseases of esophagus |
| K23 | Disorders of esophagus in diseases classified elsewhere |
| K250 | Acute gastric ulcer with hemorrhage |
| K252 | Acute gastric ulcer with both hemorrhage and perforation |
| K254 | Chronic or unspecified gastric ulcer with hemorrhage |
| K256 | Chronic or unspecified gastric ulcer with both hemorrhage and perforation |
| K260 | Acute duodenal ulcer with hemorrhage |
| K262 | Acute duodenal ulcer with both hemorrhage and perforation |
| K264 | Chronic or unspecified duodenal ulcer with hemorrhage |
| K266 | Chronic or unspecified duodenal ulcer with both hemorrhage and perforation |
| K270 | Acute peptic ulcer, site unspecified, with hemorrhage |
| K272 | Acute peptic ulcer, site unspecified, with both hemorrhage and perforation |
| K274 | Chronic or unspecified peptic ulcer, site unspecified, with hemorrhage |
| K276 | Chronic or unspecified peptic ulcer, site unspecified, with both hemorrhage and perforation |
| K280 | Acute gastrojejunal ulcer with hemorrhage |
| K282 | Acute gastrojejunal ulcer with both hemorrhage and perforation |
| K284 | Chronic or unspecified gastrojejunal ulcer with hemorrhage |
| K286 | Chronic or unspecified gastrojejunal ulcer with both hemorrhage and perforation |
| K2901 | Acute gastritis with bleeding |
| K2921 | Alcoholic gastritis with bleeding |
| K2931 | Chronic superficial gastritis with bleeding |
| K2941 | Chronic atrophic gastritis with bleeding |
| K2951 | Unspecified chronic gastritis with bleeding |
| K2961 | Other gastritis with bleeding |
| K2971 | Gastritis, unspecified, with bleeding |
| K2981 | Duodenitis with bleeding |
| K2991 | Gastroduodenitis, unspecified, with bleeding |
| K31811 | Angiodysplasia of stomach and duodenum with bleeding |
| K5521 | Angiodysplasia of colon with hemorrhage |
| K5701 | Diverticulitis of small intestine with perforation and abscess with bleeding |
| K5711 | Diverticulosis of small intestine without perforation or abscess with bleeding |
| K5713 | Diverticulitis of small intestine without perforation or abscess with bleeding |
| K5721 | Diverticulitis of large intestine with perforation and abscess with bleeding |
| K5731 | Diverticulosis of large intestine without perforation or abscess with bleeding |
| K5733 | Diverticulitis of large intestine without perforation or abscess with bleeding |
| K5741 | Diverticulitis of both small and large intestine with perforation and abscess with bleeding |
| K5751 | Diverticulosis of both small and large intestine without perforation or abscess with bleeding |
| K5753 | Diverticulitis of both small and large intestine without perforation or abscess with bleeding |
| K5781 | Diverticulitis of intestine, part unspecified, with perforation and abscess with bleeding |
| K5791 | Diverticulosis of intestine, part unspecified, without perforation or abscess with bleeding |
| K5793 | Diverticulitis of intestine, part unspecified, without perforation or abscess with bleeding |
| K625 | Hemorrhage of anus and rectum |
| K920 | Hematemesis |
| K921 | Melena |
| K922 | Gastrointestinal hemorrhage, unspecified |
| M9689 | Other intraoperative and postprocedural complications and disorders of the musculoskeletal system |
| N981 | Hyperstimulation of ovaries |
| N982 | Complications of attempted introduction of fertilized ovum following in vitro fertilization |
| N983 | Complications of attempted introduction of embryo in embryo transfer |
| N988 | Other complications associated with artificial fertilization |
| N989 | Complication associated with artificial fertilization, unspecified |
| P541 | Neonatal melena |
| P542 | Neonatal rectal hemorrhage |
| P543 | Other neonatal gastrointestinal hemorrhage |
| T8110XA | Postprocedural shock unspecified, initial encounter |
| T8111XA | Postprocedural cardiogenic shock, initial encounter |
| T8112XA | Postprocedural septic shock, initial encounter |
| T8119XA | Other postprocedural shock, initial encounter |
| T8182XA | Emphysema (subcutaneous) resulting from a procedure, initial encounter |
| T8189XA | Other complications of procedures, not elsewhere classified, initial encounter |
| T819XXA | Unspecified complication of procedure, initial encounter |
| |
| PDX Collection 0530:9 codes |
| E40 | Kwashiorkor |
| E41 | Nutritional marasmus |
| E42 | Marasmic kwashiorkor |
| E43 | Unspecified severe protein-calorie malnutrition |
| E440 | Moderate protein-calorie malnutrition |
| E441 | Mild protein-calorie malnutrition |
| E45 | Retarded development following protein-calorie malnutrition |
| E46 | Unspecified protein-calorie malnutrition |
| E640 | Sequelae of protein-calorie malnutrition |
| |
| PDX Collection 0531:34 codes |
| D81818 | Other biotin-dependent carboxylase deficiency |
| D81819 | Biotin-dependent carboxylase deficiency, unspecified |
| E5111 | Dry beriberi |
| E5112 | Wet beriberi |
| E512 | Wernicke's encephalopathy |
| E518 | Other manifestations of thiamine deficiency |
| E519 | Thiamine deficiency, unspecified |
| E52 | Niacin deficiency [pellagra] |
| E530 | Riboflavin deficiency |
| E531 | Pyridoxine deficiency |
| E538 | Deficiency of other specified B group vitamins |
| E539 | Vitamin B deficiency, unspecified |
| E560 | Deficiency of vitamin E |
| E568 | Deficiency of other vitamins |
| E569 | Vitamin deficiency, unspecified |
| E58 | Dietary calcium deficiency |
| E59 | Dietary selenium deficiency |
| E60 | Dietary zinc deficiency |
| E610 | Copper deficiency |
| E611 | Iron deficiency |
| E612 | Magnesium deficiency |
| E613 | Manganese deficiency |
| E614 | Chromium deficiency |
| E615 | Molybdenum deficiency |
| E616 | Vanadium deficiency |
| E617 | Deficiency of multiple nutrient elements |
| E618 | Deficiency of other specified nutrient elements |
| E619 | Deficiency of nutrient element, unspecified |
| E630 | Essential fatty acid [EFA] deficiency |
| E631 | Imbalance of constituents of food intake |
| E638 | Other specified nutritional deficiencies |
| E639 | Nutritional deficiency, unspecified |
| E648 | Sequelae of other nutritional deficiencies |
| E649 | Sequelae of unspecified nutritional deficiency |
| |
| PDX Collection 0532:34 codes |
| E550 | Rickets, active |
| E559 | Vitamin D deficiency, unspecified |
| E560 | Deficiency of vitamin E |
| E561 | Deficiency of vitamin K |
| E568 | Deficiency of other vitamins |
| E569 | Vitamin deficiency, unspecified |
| E58 | Dietary calcium deficiency |
| E59 | Dietary selenium deficiency |
| E60 | Dietary zinc deficiency |
| E610 | Copper deficiency |
| E611 | Iron deficiency |
| E612 | Magnesium deficiency |
| E613 | Manganese deficiency |
| E614 | Chromium deficiency |
| E615 | Molybdenum deficiency |
| E616 | Vanadium deficiency |
| E617 | Deficiency of multiple nutrient elements |
| E618 | Deficiency of other specified nutrient elements |
| E619 | Deficiency of nutrient element, unspecified |
| E630 | Essential fatty acid [EFA] deficiency |
| E631 | Imbalance of constituents of food intake |
| E638 | Other specified nutritional deficiencies |
| E639 | Nutritional deficiency, unspecified |
| E643 | Sequelae of rickets |
| E648 | Sequelae of other nutritional deficiencies |
| E649 | Sequelae of unspecified nutritional deficiency |
| M830 | Puerperal osteomalacia |
| M831 | Senile osteomalacia |
| M832 | Adult osteomalacia due to malabsorption |
| M833 | Adult osteomalacia due to malnutrition |
| M834 | Aluminum bone disease |
| M835 | Other drug-induced osteomalacia in adults |
| M838 | Other adult osteomalacia |
| M839 | Adult osteomalacia, unspecified |
| |
| PDX Collection 0533:7 codes |
| E662 | Morbid (severe) obesity with alveolar hypoventilation |
| I270 | Primary pulmonary hypertension |
| I271 | Kyphoscoliotic heart disease |
| I272 | Other secondary pulmonary hypertension |
| I2781 | Cor pulmonale (chronic) |
| I2789 | Other specified pulmonary heart diseases |
| I279 | Pulmonary heart disease, unspecified |
| |
| PDX Collection 0534:115 codes |
| C880 | Waldenström 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 |
| E708 | 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 | Hyperoxaluria |
| E7259 | Other disorders of glycine metabolism |
| E728 | 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 |
| 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 |
| E748 | 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 |
| E780 | Pure hypercholesterolemia |
| E781 | Pure hyperglyceridemia |
| E782 | Mixed hyperlipidemia |
| E783 | Hyperchylomicronemia |
| E784 | 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 |
| 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 0535:33 codes |
| C965 | Multifocal and unisystemic Langerhans-cell histiocytosis |
| C966 | Unifocal Langerhans-cell histiocytosis |
| E7139 | Other disorders of fatty-acid metabolism |
| E7140 | Disorder of carnitine metabolism, unspecified |
| E7141 | Primary carnitine deficiency |
| E7142 | Carnitine deficiency due to inborn errors of metabolism |
| E7143 | Iatrogenic carnitine deficiency |
| E71440 | Ruvalcaba-Myhre-Smith syndrome |
| E71448 | Other secondary carnitine deficiency |
| E7150 | Peroxisomal disorder, unspecified |
| E71510 | Zellweger syndrome |
| E71511 | Neonatal adrenoleukodystrophy |
| E71518 | Other disorders of peroxisome biogenesis |
| E71520 | Childhood cerebral X-linked adrenoleukodystrophy |
| E71521 | Adolescent X-linked adrenoleukodystrophy |
| E71522 | Adrenomyeloneuropathy |
| E71528 | Other X-linked adrenoleukodystrophy |
| E71529 | X-linked adrenoleukodystrophy, unspecified type |
| E7153 | Other group 2 peroxisomal disorders |
| E71540 | Rhizomelic chondrodysplasia punctata |
| E71541 | Zellweger-like syndrome |
| E71542 | Other group 3 peroxisomal disorders |
| E71548 | Other peroxisomal disorders |
| E803 | Defects of catalase and peroxidase |
| E8840 | Mitochondrial metabolism disorder, unspecified |
| E8841 | MELAS syndrome |
| E8842 | MERRF syndrome |
| E8849 | Other mitochondrial metabolism disorders |
| E8889 | Other specified metabolic disorders |
| H49811 | Kearns-Sayre syndrome, right eye |
| H49812 | Kearns-Sayre syndrome, left eye |
| H49813 | Kearns-Sayre syndrome, bilateral |
| H49819 | Kearns-Sayre syndrome, unspecified eye |
| |
| PDX Collection 0536:30 codes |
| C965 | Multifocal and unisystemic Langerhans-cell histiocytosis |
| C966 | Unifocal Langerhans-cell histiocytosis |
| E71310 | Long chain/very long chain acyl CoA dehydrogenase deficiency |
| E71311 | Medium chain acyl CoA dehydrogenase deficiency |
| E71312 | Short chain acyl CoA dehydrogenase deficiency |
| E71313 | Glutaric aciduria type II |
| E71314 | Muscle carnitine palmitoyltransferase deficiency |
| E71318 | Other disorders of fatty-acid oxidation |
| E7132 | Disorders of ketone metabolism |
| E7139 | Other disorders of fatty-acid metabolism |
| E7140 | Disorder of carnitine metabolism, unspecified |
| E7141 | Primary carnitine deficiency |
| E7142 | Carnitine deficiency due to inborn errors of metabolism |
| E7143 | Iatrogenic carnitine deficiency |
| E71440 | Ruvalcaba-Myhre-Smith syndrome |
| E71448 | Other secondary carnitine deficiency |
| E803 | Defects of catalase and peroxidase |
| E804 | Gilbert syndrome |
| E805 | Crigler-Najjar syndrome |
| E806 | Other disorders of bilirubin metabolism |
| E807 | Disorder of bilirubin metabolism, unspecified |
| E8840 | Mitochondrial metabolism disorder, unspecified |
| E8841 | MELAS syndrome |
| E8842 | MERRF syndrome |
| E8849 | Other mitochondrial metabolism disorders |
| E8889 | Other specified metabolic disorders |
| H49811 | Kearns-Sayre syndrome, right eye |
| H49812 | Kearns-Sayre syndrome, left eye |
| H49813 | Kearns-Sayre syndrome, bilateral |
| H49819 | Kearns-Sayre syndrome, unspecified eye |
| |
| PDX Collection 0537:27 codes |
| E7500 | GM2 gangliosidosis, unspecified |
| E7501 | Sandhoff disease |
| E7502 | Tay-Sachs disease |
| E7509 | Other GM2 gangliosidosis |
| E7510 | Unspecified gangliosidosis |
| E7511 | Mucolipidosis IV |
| E7519 | Other gangliosidosis |
| E754 | Neuronal ceroid lipofuscinosis |
| F842 | Rett's syndrome |
| G132 | Systemic atrophy primarily affecting the central nervous system in myxedema |
| G138 | Systemic atrophy primarily affecting central nervous system in other diseases classified elsewhere |
| G300 | Alzheimer's disease with early onset |
| G301 | Alzheimer's disease with late onset |
| G308 | Other Alzheimer's disease |
| G309 | Alzheimer's disease, unspecified |
| G3101 | Pick's disease |
| G3109 | Other frontotemporal dementia |
| G311 | Senile degeneration of brain, not elsewhere classified |
| G312 | Degeneration of nervous system due to alcohol |
| G3181 | Alpers disease |
| G3182 | Leigh's disease |
| G3184 | Mild cognitive impairment, so stated |
| G3185 | Corticobasal degeneration |
| G3189 | Other specified degenerative diseases of nervous system |
| G319 | Degenerative disease of nervous system, unspecified |
| G914 | Hydrocephalus in diseases classified elsewhere |
| G94 | Other disorders of brain in diseases classified elsewhere |
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