15,083 codes
CC codes (complication or comorbidity)
Secondary diagnoses that raise an inpatient stay to the middle-severity MS-DRG in a family, unless excluded for the principal diagnosis. Source: MS-DRG v44 Definitions Manual, Appendix C.
Chapter 4: Endocrine, nutritional and metabolic diseases
- E06.0Acute thyroiditis
- E08.52Diabetes mellitus due to underlying condition with diabetic peripheral angiopathy with gangrene
- E09.52Drug or chemical induced diabetes mellitus with diabetic peripheral angiopathy with gangrene
- E10.52Type 1 diabetes mellitus with diabetic peripheral angiopathy with gangrene
- E11.52Type 2 diabetes mellitus with diabetic peripheral angiopathy with gangrene
- E13.52Other specified diabetes mellitus with diabetic peripheral angiopathy with gangrene
- E15Nondiabetic hypoglycemic coma
- E22.1Hyperprolactinemia
- E22.2Syndrome of inappropriate secretion of antidiuretic hormone
- E22.8Other hyperfunction of pituitary gland
- E22.9Hyperfunction of pituitary gland, unspecified
- E23.0Hypopituitarism
- E23.2Diabetes insipidus
- E24.0Pituitary-dependent Cushing's disease
- E24.2Drug-induced Cushing's syndrome
- E24.3Ectopic ACTH syndrome
- E24.4Alcohol-induced pseudo-Cushing's syndrome
- E24.8Other Cushing's syndrome
- E24.9Cushing's syndrome, unspecified
- E27.0Other adrenocortical overactivity
- E27.1Primary adrenocortical insufficiency
- E27.2Addisonian crisis
- E27.3Drug-induced adrenocortical insufficiency
- E27.40Unspecified adrenocortical insufficiency
- E27.49Other adrenocortical insufficiency
- E27.5Adrenomedullary hyperfunction
- E32.1Abscess of thymus
- E34.00Carcinoid syndrome, unspecified
- E34.01Carcinoid heart syndrome
- E34.09Other carcinoid syndrome
- E36.01Intraoperative hemorrhage and hematoma of an endocrine system organ or structure complicating an endocrine system procedure
- E36.02Intraoperative hemorrhage and hematoma of an endocrine system organ or structure complicating other procedure
- E36.11Accidental puncture and laceration of an endocrine system organ or structure during an endocrine system procedure
- E36.12Accidental puncture and laceration of an endocrine system organ or structure during other procedure
- E44.0Moderate protein-calorie malnutrition
- E44.1Mild protein-calorie malnutrition
- E45Retarded development following protein-calorie malnutrition
- E46Unspecified protein-calorie malnutrition
- E51.11Dry beriberi
- E51.12Wet beriberi
- E51.2Wernicke's encephalopathy
- E51.8Other manifestations of thiamine deficiency
- E51.9Thiamine deficiency, unspecified
- E53.0Riboflavin deficiency
- E55.0Rickets, active
- E64.0Sequelae of protein-calorie malnutrition
- E66.2Morbid (severe) obesity with alveolar hypoventilation
- E70.0Classical phenylketonuria
- E70.1Other hyperphenylalaninemias
- E70.20Disorder of tyrosine metabolism, unspecified
- E70.21Tyrosinemia
- E70.29Other disorders of tyrosine metabolism
- E70.30Albinism, unspecified
- E70.310X-linked ocular albinism
- E70.311Autosomal recessive ocular albinism
- E70.318Other ocular albinism
- E70.319Ocular albinism, unspecified
- E70.320Tyrosinase negative oculocutaneous albinism
- E70.321Tyrosinase positive oculocutaneous albinism
- E70.328Other oculocutaneous albinism
- E70.329Oculocutaneous albinism, unspecified
- E70.330Chediak-Higashi syndrome
- E70.331Hermansky-Pudlak syndrome
- E70.338Other albinism with hematologic abnormality
- E70.339Albinism with hematologic abnormality, unspecified
- E70.39Other specified albinism
- E70.40Disorders of histidine metabolism, unspecified
- E70.41Histidinemia
- E70.49Other disorders of histidine metabolism
- E70.5Disorders of tryptophan metabolism
- E70.81Aromatic L-amino acid decarboxylase deficiency
- E70.89Other disorders of aromatic amino-acid metabolism
- E70.9Disorder of aromatic amino-acid metabolism, unspecified
- E71.0Maple-syrup-urine disease
- E71.110Isovaleric acidemia
- E71.1113-methylglutaconic aciduria
- E71.118Other branched-chain organic acidurias
- E71.120Methylmalonic acidemia
- E71.121Propionic acidemia
- E71.128Other disorders of propionate metabolism
- E71.19Other disorders of branched-chain amino-acid metabolism
- E71.2Disorder of branched-chain amino-acid metabolism, unspecified
- E71.310Long chain/very long chain acyl CoA dehydrogenase deficiency
- E71.311Medium chain acyl CoA dehydrogenase deficiency
- E71.312Short chain acyl CoA dehydrogenase deficiency
- E71.313Glutaric aciduria type II
- E71.314Muscle carnitine palmitoyltransferase deficiency
- E71.318Other disorders of fatty-acid oxidation
- E71.32Disorders of ketone metabolism
- E71.39Other disorders of fatty-acid metabolism
- E71.50Peroxisomal disorder, unspecified
- E71.510Zellweger syndrome
- E71.511Neonatal adrenoleukodystrophy
- E71.518Other disorders of peroxisome biogenesis
- E71.520Childhood cerebral X-linked adrenoleukodystrophy
- E71.521Adolescent X-linked adrenoleukodystrophy
- E71.522Adrenomyeloneuropathy
- E71.528Other X-linked adrenoleukodystrophy
- E71.529X-linked adrenoleukodystrophy, unspecified type
- E71.53Other group 2 peroxisomal disorders
- E71.540Rhizomelic chondrodysplasia punctata
- E71.541Zellweger-like syndrome
- E71.542Other group 3 peroxisomal disorders
- E71.548Other peroxisomal disorders
- E72.00Disorders of amino-acid transport, unspecified
- E72.01Cystinuria
- E72.02Hartnup's disease
- E72.03Lowe's syndrome
- E72.04Cystinosis
- E72.09Other disorders of amino-acid transport
- E72.10Disorders of sulfur-bearing amino-acid metabolism, unspecified
- E72.11Homocystinuria
- E72.12Methylenetetrahydrofolate reductase deficiency
- E72.19Other disorders of sulfur-bearing amino-acid metabolism
- E72.20Disorder of urea cycle metabolism, unspecified
- E72.21Argininemia
- E72.22Arginosuccinic aciduria
- E72.23Citrullinemia
- E72.29Other disorders of urea cycle metabolism
- E72.3Disorders of lysine and hydroxylysine metabolism
- E72.4Disorders of ornithine metabolism
- E72.50Disorder of glycine metabolism, unspecified
- E72.51Non-ketotic hyperglycinemia
- E72.52Trimethylaminuria
- E72.530Primary hyperoxaluria, type 1
- E72.538Other specified primary hyperoxaluria
- E72.539Primary hyperoxaluria, unspecified
- E72.59Other disorders of glycine metabolism
- E72.81Disorders of gamma aminobutyric acid metabolism
- E72.89Other specified disorders of amino-acid metabolism
- E72.9Disorder of amino-acid metabolism, unspecified
- E74.00Glycogen storage disease, unspecified
- E74.01von Gierke disease
- E74.02Pompe disease
- E74.03Cori disease
- E74.04McArdle disease
- E74.05Lysosome-associated membrane protein 2 [LAMP2] deficiency
- E74.09Other glycogen storage disease
- E74.20Disorders of galactose metabolism, unspecified
- E74.21Galactosemia
- E74.29Other disorders of galactose metabolism
- E74.4Disorders of pyruvate metabolism and gluconeogenesis
- E74.810Glucose transporter protein type 1 deficiency
- E74.818Other disorders of glucose transport
- E74.819Disorders of glucose transport, unspecified
- E74.820SLC13A5 Citrate Transporter Disorder
- E74.829Other disorders of citrate metabolism
- E74.89Other specified disorders of carbohydrate metabolism
- E75.00GM2 gangliosidosis, unspecified
- E75.01Sandhoff disease
- E75.02Tay-Sachs disease
- E75.09Other GM2 gangliosidosis
- E75.10Unspecified gangliosidosis
- E75.11Mucolipidosis IV
- E75.19Other gangliosidosis
- E75.23Krabbe disease
- E75.25Metachromatic leukodystrophy
- E75.26Sulfatase deficiency
- E75.27Pelizaeus-Merzbacher disease
- E75.28Canavan disease
- E75.29Other sphingolipidosis
- E75.4Neuronal ceroid lipofuscinosis
- E76.01Hurler's syndrome
- E76.02Hurler-Scheie syndrome
- E76.03Scheie's syndrome
- E76.1Mucopolysaccharidosis, type II
- E76.210Morquio A mucopolysaccharidoses
- E76.211Morquio B mucopolysaccharidoses
- E76.219Morquio mucopolysaccharidoses, unspecified
- E76.22Sanfilippo mucopolysaccharidoses
- E76.29Other mucopolysaccharidoses
- E76.3Mucopolysaccharidosis, unspecified
- E76.8Other disorders of glucosaminoglycan metabolism
- E76.9Glucosaminoglycan metabolism disorder, unspecified
- E78.71Barth syndrome
- E78.72Smith-Lemli-Opitz syndrome
- E79.1Lesch-Nyhan syndrome
- E79.2Myoadenylate deaminase deficiency
- E79.81Aicardi-Goutieres syndrome
- E79.82Hereditary xanthinuria
- E79.89Other specified disorders of purine and pyrimidine metabolism
- E79.9Disorder of purine and pyrimidine metabolism, unspecified
- E80.0Hereditary erythropoietic porphyria
- E80.1Porphyria cutanea tarda
- E80.20Unspecified porphyria
- E80.21Acute intermittent (hepatic) porphyria
- E80.29Other porphyria
- E80.3Defects of catalase and peroxidase
- E83.820Generalized arterial calcification of infancy with unspecified genetic causality
- E83.821ENPP1 deficiency causing generalized arterial calcification of infancy
- E83.823ABCC6 deficiency causing generalized arterial calcification of infancy
- E83.825CD73 deficiency causing arterial calcification
- E84.19Cystic fibrosis with other intestinal manifestations
- E84.8Cystic fibrosis with other manifestations
- E84.9Cystic fibrosis, unspecified
- E85.0Non-neuropathic heredofamilial amyloidosis
- E85.1Neuropathic heredofamilial amyloidosis
- E85.2Heredofamilial amyloidosis, unspecified
- E85.3Secondary systemic amyloidosis
- E85.4Organ-limited amyloidosis
- E85.81Light chain (AL) amyloidosis
- E85.82Wild-type transthyretin-related (ATTR) amyloidosis
- E85.89Other amyloidosis
- E85.9Amyloidosis, unspecified
- E87.0Hyperosmolality and hypernatremia
- E87.1Hypo-osmolality and hyponatremia
- E87.20Acidosis, unspecified
- E87.21Acute metabolic acidosis
- E87.22Chronic metabolic acidosis
- E87.29Other acidosis
- E87.3Alkalosis
- E87.4Mixed disorder of acid-base balance
- E88.02Plasminogen deficiency
- E88.40Mitochondrial metabolism disorder, unspecified
- E88.41MELAS syndrome
- E88.42MERRF syndrome
- E88.43Disorders of mitochondrial tRNA synthetases
- E88.49Other mitochondrial metabolism disorders
- E89.1Postprocedural hypoinsulinemia
- E89.6Postprocedural adrenocortical (-medullary) hypofunction
- E89.810Postprocedural hemorrhage of an endocrine system organ or structure following an endocrine system procedure
- E89.811Postprocedural hemorrhage of an endocrine system organ or structure following other procedure
- E89.820Postprocedural hematoma of an endocrine system organ or structure following an endocrine system procedure
- E89.821Postprocedural hematoma of an endocrine system organ or structure following other procedure
- E89.822Postprocedural seroma of an endocrine system organ or structure following an endocrine system procedure
- E89.823Postprocedural seroma of an endocrine system organ or structure following other procedure
- E89.830Post bariatric hypoglycemia
- E89.838Other postprocedural hypoglycemia
- E89.89Other postprocedural endocrine and metabolic complications and disorders