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JB64.2 Endocrine, nutritional or metabolic diseases complicating pregnancy, childbirth or the puerperium International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01 Any disease affecting pregnant females, characterised by endocrine, nutrition, or metabolic manifestations that complicate pregnancy, childbirth, or the puerperium.
exclusions coding note This category includes conditions which complicate the pregnant state, are aggravated by the pregnancy or are a main reason for obstetric care but no specific category exists in this chapter.
postcoordination Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
Associated with - multiple selections are allowed [select] 5A00 Hypothyroidism – 5A00.0 Congenital hypothyroidism – 5A00.1 Iodine-deficiency-related thyroid disorders or allied conditions – 5A00.2 Acquired hypothyroidism – 5A00.Z Hypothyroidism, unspecified –– 5A00.00 Permanent congenital hypothyroidism with diffuse goitre –– 5A00.01 Permanent congenital hypothyroidism without goitre –– 5A00.02 Pendred syndrome –– 5A00.03 Transient congenital hypothyroidism –– 5A00.04 Congenital hypothyroidism due to iodine deficiency –– 5A00.0Y Other specified congenital hypothyroidism –– 5A00.0Z Congenital hypothyroidism, unspecified –– 5A00.10 Iodine-deficiency-related diffuse goitre –– 5A00.11 Iodine-deficiency-related multinodular goitre –– 5A00.1Z Iodine-deficiency-related thyroid disorders or allied conditions, unspecified –– 5A00.20 Hypothyroidism due to medicaments or other exogenous substances –– 5A00.21 Myxoedema coma –– 5A00.22 Subclinical iodine-deficiency hypothyroidism –– 5A00.2Y Other specified acquired hypothyroidism –– 5A00.2Z Acquired hypothyroidism, unspecified 5A01 Nontoxic goitre – 5A01.0 Nontoxic diffuse goitre – 5A01.1 Nontoxic single thyroid nodule – 5A01.2 Nontoxic multinodular goitre – 5A01.Z Nontoxic goitre, unspecified 5A02 Thyrotoxicosis – 5A02.0 Thyrotoxicosis with diffuse goitre – 5A02.1 Thyrotoxicosis with toxic single thyroid nodule – 5A02.2 Thyrotoxicosis with toxic multinodular goitre – 5A02.3 Thyrotoxicosis from ectopic thyroid tissue – 5A02.4 Thyrotoxicosis factitia – 5A02.5 Thyroid crisis – 5A02.6 Secondary hyperthyroidism – 5A02.Y Other specified thyrotoxicosis – 5A02.Z Thyrotoxicosis, unspecified 5A03 Thyroiditis – 5A03.0 Acute thyroiditis – 5A03.1 Subacute thyroiditis – 5A03.2 Autoimmune thyroiditis – 5A03.Y Other specified thyroiditis – 5A03.Z Thyroiditis, unspecified –– 5A03.20 Hashimoto thyroiditis –– 5A03.21 Painless thyroiditis –– 5A03.2Y Other specified autoimmune thyroiditis –– 5A03.2Z Autoimmune thyroiditis, unspecified 5A04 Hypersecretion of calcitonin 5A05 Generalised resistance to thyroid hormone 5A06 Sick-euthyroid syndrome 5A0Y Other specified disorders of the thyroid gland or thyroid hormones system 5A0Z Disorders of the thyroid gland or thyroid hormones system, unspecified 5A10 Type 1 diabetes mellitus 5A11 Type 2 diabetes mellitus 5A12 Malnutrition-related diabetes mellitus 5A13 Diabetes mellitus, other specified type – 5A13.0 Diabetes mellitus due to genetic defects of beta cell function – 5A13.1 Diabetes mellitus due to genetic defects in insulin action – 5A13.2 Diabetes mellitus due to diseases of the exocrine pancreas – 5A13.3 Diabetes mellitus due to endocrinopathies – 5A13.4 Diabetes mellitus due to drug or chemical – 5A13.5 Diabetes mellitus due to uncommon forms of immune-mediated diabetes – 5A13.6 Diabetes mellitus due to other genetic syndromes – 5A13.7 Diabetes mellitus due to clinically defined subtypes or syndromes – 5A13.Y Diabetes mellitus due to other specified cause 5A14 Diabetes mellitus, type unspecified – 5A20 Diabetic hyperosmolar hyperglycaemic state –– 5A20.0 Hyperosmolar hyperglycaemic state without coma –– 5A20.1 Hyperosmolar hyperglycaemic state with coma –– 5A20.Z Diabetic hyperosmolar hyperglycaemic state, unspecified – 5A21 Hypoglycaemia in the context of diabetes mellitus –– 5A21.0 Hypoglycaemia in the context of diabetes mellitus without coma –– 5A21.1 Hypoglycaemia in the context of diabetes mellitus with coma –– 5A21.Z Hypoglycaemia in the context of diabetes, unspecified – 5A22 Diabetic acidosis –– 5A22.0 Diabetic ketoacidosis without coma –– 5A22.1 Diabetic lactic acidosis –– 5A22.2 Diabetic metabolic acidosis –– 5A22.3 Diabetic ketoacidosis with coma –– 5A22.Y Other specified diabetic acidosis –– 5A22.Z Diabetic acidosis, unspecified – 5A23 Diabetic coma – 5A24 Uncontrolled or unstable diabetes mellitus – 5A2Y Other specified acute complications of diabetes mellitus 5A40 Intermediate hyperglycaemia – 5A40.0 Impaired fasting glucose – 5A40.1 Impaired glucose tolerance – 5A40.Y Other specified intermediate hyperglycaemia – 5A40.Z Intermediate hyperglycaemia, unspecified 5A41 Hypoglycaemia without associated diabetes 5A42 Increased secretion of glucagon 5A43 Abnormal secretion of gastrin – 5A43.0 Drug-induced hypergastrinaemia – 5A43.1 Zollinger-Ellison syndrome – 5A43.Y Other specified abnormal secretion of gastrin – 5A43.Z Abnormal secretion of gastrin, unspecified 5A44 Insulin-resistance syndromes 5A45 Persistent hyperinsulinaemic hypoglycaemia of infancy 5A4Y Other specified disorders of glucose regulation or pancreatic internal secretion 5A4Z Disorders of glucose regulation or pancreatic internal secretion, unspecified 5A50 Hypoparathyroidism – 5A50.0 Hypoparathyroidism due to impaired parathyroid hormone secretion – 5A50.1 Pseudohypoparathyroidism – 5A50.Y Other specified hypoparathyroidism – 5A50.Z Hypoparathyroidism, unspecified –– 5A50.00 Idiopathic hypoparathyroidism –– 5A50.01 Secondary hypoparathyroidism –– 5A50.02 Hypoparathyroidism due to destruction of the parathyroid glands –– 5A50.03 Autoimmune hypoparathyroidism –– 5A50.0Y Other specified hypoparathyroidism due to impaired parathyroid hormone secretion –– 5A50.0Z Hypoparathyroidism due to impaired parathyroid hormone secretion, unspecified 5A51 Hyperparathyroidism – 5A51.0 Primary hyperparathyroidism – 5A51.1 Secondary hyperparathyroidism – 5A51.2 Familial hypocalciuric hypercalcaemia – 5A51.Y Other specified hyperparathyroidism – 5A51.Z Hyperparathyroidism, unspecified 5A5Y Other specified disorders of the parathyroids or parathyroid hormone system 5A5Z Disorders of the parathyroids or parathyroid hormone system, unspecified 5A60 Hyperfunction of pituitary gland – 5A60.0 Acromegaly or pituitary gigantism – 5A60.1 Hyperprolactinaemia – 5A60.2 Syndrome of inappropriate secretion of antidiuretic hormone – 5A60.3 Central precocious puberty – 5A60.Y Other specified hyperfunction of pituitary gland – 5A60.Z Hyperfunction of pituitary gland, unspecified –– 5A60.20 Nephrogenic syndrome of inappropriate antidiuresis –– 5A60.2Y Other specified syndrome of inappropriate secretion of antidiuretic hormone –– 5A60.2Z Syndrome of inappropriate secretion of antidiuretic hormone, unspecified 5A61 Hypofunction or certain other specified disorders of pituitary gland – 5A61.0 Hypopituitarism – 5A61.1 Adrenocorticotropic hormone deficiency – 5A61.2 Gonadotropin deficiency – 5A61.3 Growth hormone deficiency – 5A61.4 Thyroid stimulating hormone deficiency – 5A61.5 Central diabetes insipidus – 5A61.6 Oxytocin deficiency – 5A61.Y Other specified hypofunction or disorders of pituitary gland –– 5A61.40 Acquired central hypothyroidism –– 5A61.41 Congenital central hypothyroidism –– 5A61.4Y Other specified thyroid stimulating hormone deficiency –– 5A61.4Z Thyroid stimulating hormone deficiency, unspecified 5A6Z Disorders of the pituitary hormone system, unspecified 5A70 Cushing syndrome – 5A70.0 Pituitary-dependent Cushing disease – 5A70.1 Ectopic ACTH syndrome – 5A70.2 Pseudo-Cushing syndrome – 5A70.3 Nelson syndrome – 5A70.Y Other specified Cushing syndrome – 5A70.Z Cushing syndrome, unspecified 5A71 Adrenogenital disorders – 5A71.0 46,XX disorders of sex development induced by androgens of fetal origin – 5A71.1 46,XX disorders of sex development induced by androgens of maternal origin – 5A71.Y Other specified adrenogenital disorders – 5A71.Z Adrenogenital disorders, unspecified –– 5A71.00 Glucocorticoid resistance –– 5A71.01 Congenital adrenal hyperplasia –– 5A71.0Y Other specified 46,XX disorders of sex development induced by androgens of fetal origin –– 5A71.0Z 46,XX disorders of sex development induced by androgens of fetal origin, unspecified 5A72 Hyperaldosteronism – 5A72.0 Primary hyperaldosteronism – 5A72.1 Secondary hyperaldosteronism – 5A72.Z Hyperaldosteronism, unspecified 5A73 Hypoaldosteronism 5A74 Adrenocortical insufficiency – 5A74.0 Acquired adrenocortical insufficiency – 5A74.1 Adrenal crisis – 5A74.Y Other specified adrenocortical insufficiency – 5A74.Z Adrenocortical insufficiency, unspecified 5A75 Adrenomedullary hyperfunction 5A76 Certain specified disorders of adrenal gland – 5A76.0 Premature adrenarche – 5A76.Y Other specified disorders of adrenal gland 5A7Z Disorders of the adrenal glands or adrenal hormone system, unspecified 5A80 Ovarian dysfunction – 5A80.0 Clinical hyperandrogenism – 5A80.1 Polycystic ovary syndrome – 5A80.2 Polycystic ovary – 5A80.3 Anovulation – 5A80.4 Oligo-ovulation – 5A80.5 Diminished ovarian reserve – 5A80.Y Other specified ovarian dysfunction – 5A80.Z Ovarian dysfunction, unspecified 5A81 Testicular dysfunction or testosterone-related disorders – 5A81.0 Testicular hyperfunction – 5A81.1 Testicular hypofunction – 5A81.Y Other specified testicular dysfunction or testosterone-related disorders – 5A81.Z Testicular dysfunction or testosterone-related disorders, unspecified 5A8Z Disorders of the gonadal hormone system, unspecified 5A90 Disorder of puberty due to oestrogen resistance 5A91 Delayed puberty 5A92 Peripheral precocious puberty 5A9Y Other disorders of puberty 5A9Z Disorders of puberty, unspecified 5B00 Autoimmune polyendocrinopathy 5B01 Polyglandular hyperfunction 5B0Y Other specified polyglandular dysfunction 5B0Z Polyglandular dysfunction, unspecified 5B10 Carcinoid syndrome 5B11 Short stature, not elsewhere classified 5B12 Constitutional tall stature 5B1Y Other specified endocrine disorders, not elsewhere classified 5B3Y Other specified endocrine diseases 5B3Z Endocrine diseases, unspecified 5B50 Underweight in infants, children or adolescents 5B51 Wasting in infants, children or adolescents 5B52 Acute malnutrition in infants, children or adolescents 5B53 Stunting in infants, children or adolescents 5B54 Underweight in adults 5B55 Vitamin A deficiency – 5B55.0 Vitamin A deficiency with night blindness – 5B55.1 Vitamin A deficiency with conjunctival xerosis – 5B55.2 Vitamin A deficiency with conjunctival xerosis and Bitot's spots – 5B55.3 Vitamin A deficiency with corneal xerosis – 5B55.4 Vitamin A deficiency with corneal ulceration or keratomalacia – 5B55.5 Vitamin A deficiency with xerophthalmic scars of cornea or blindness – 5B55.Y Vitamin A deficiency with other specified manifestations – 5B55.Z Vitamin A deficiency, unspecified 5B56 Vitamin C deficiency – 5B56.0 Scurvy – 5B56.Y Other specified vitamin C deficiency – 5B56.Z Vitamin C deficiency, unspecified 5B57 Vitamin D deficiency – 5B57.0 Vitamin D deficiency rickets – 5B57.1 Vitamin D deficiency osteomalacia – 5B57.Y Other specified vitamin D deficiency – 5B57.Z Vitamin D deficiency, unspecified 5B58 Vitamin E deficiency 5B59 Vitamin K deficiency 5B5A Vitamin B1 deficiency – 5B5A.0 Beriberi – 5B5A.1 Wernicke-Korsakoff Syndrome – 5B5A.Y Other specified vitamin B1 deficiency – 5B5A.Z Vitamin B1 deficiency, unspecified –– 5B5A.00 Dry beriberi –– 5B5A.01 Wet beriberi –– 5B5A.0Z Beriberi, unspecified –– 5B5A.10 Wernicke encephalopathy –– 5B5A.11 Korsakoff syndrome –– 5B5A.1Y Other specified Wernicke-Korsakoff Syndrome –– 5B5A.1Z Wernicke-Korsakoff Syndrome, unspecified 5B5B Vitamin B2 deficiency 5B5C Vitamin B3 deficiency – 5B5C.0 Pellagra – 5B5C.Y Other specified vitamin B3 deficiency – 5B5C.Z Vitamin B3 deficiency, unspecified 5B5D Vitamin B6 deficiency 5B5E Folate deficiency 5B5F Vitamin B12 deficiency 5B5G Biotin deficiency 5B5H Pantothenic acid deficiency 5B5J Choline deficiency 5B5K Mineral deficiencies – 5B5K.0 Iron deficiency – 5B5K.1 Calcium deficiency – 5B5K.2 Zinc deficiency – 5B5K.3 Iodine deficiency – 5B5K.4 Fluorine deficiency – 5B5K.5 Sodium chloride deficiency – 5B5K.6 Copper deficiency – 5B5K.7 Selenium deficiency – 5B5K.8 Chromium deficiency – 5B5K.9 Manganese deficiency – 5B5K.A Molybdenum deficiency – 5B5K.B Vanadium deficiency – 5B5K.Y Other specified mineral deficiency – 5B5K.Z Mineral deficiency, unspecified –– 5B5K.10 Tetany due to acute calcium deficiency –– 5B5K.1Y Other specified calcium deficiency –– 5B5K.1Z Calcium deficiency, unspecified – 5B60 Sequelae of protein-energy malnutrition – 5B61 Sequelae of vitamin A deficiency – 5B62 Sequelae of vitamin C deficiency – 5B63 Sequelae of rickets – 5B6Y Other specified sequelae of malnutrition or certain specified nutritional deficiencies – 5B6Z Sequelae of malnutrition or certain specified nutritional deficiencies, unspecified 5B70 Essential fatty acid deficiency 5B71 Protein deficiency 5B7Y Other specified undernutrition 5B7Z Unspecified undernutrition – 5B80 Overweight or localised adiposity –– 5B80.0 Overweight –– 5B80.1 Localised adiposity ––– 5B80.00 Overweight in infants, children or adolescents ––– 5B80.01 Overweight in adults ––– 5B80.0Z Overweight, unspecified – 5B81 Obesity –– 5B81.0 Obesity due to energy imbalance –– 5B81.1 Drug-induced obesity –– 5B81.Y Other specified obesity –– 5B81.Z Obesity, unspecified ––– 5B81.00 Obesity in children or adolescents ––– 5B81.01 Obesity in adults – 5B90 Vitamin excesses –– 5B90.0 Hypervitaminosis A –– 5B90.1 Hypercarotenaemia –– 5B90.2 Hypervitaminosis D –– 5B90.3 Megavitamin-B6 syndrome –– 5B90.Y Other specified vitamin excess –– 5B90.Z Unspecified vitamin excesses – 5B91 Mineral excesses –– 5B91.0 Hypercalcaemia –– 5B91.1 Zinc excess –– 5B91.2 Sodium chloride excess –– 5B91.3 Fluorine excess –– 5B91.4 Aluminium excess –– 5B91.5 Manganese excess –– 5B91.Y Other specified mineral excess –– 5B91.Z Unspecified mineral excess – 5B9Y Other specified nutrient excesses – 5B9Z Certain specified nutrient excesses, unspecified 5C1Y Other specified overweight, obesity or specific nutrient excesses 5C1Z Overweight, obesity or specific nutrient excesses, unspecified 5C3Y Other specified nutritional disorders 5C3Z Nutritional disorders, unspecified 5C50 Inborn errors of amino acid or other organic acid metabolism – 5C50.0 Phenylketonuria – 5C50.1 Disorders of tyrosine metabolism – 5C50.2 Disorders of histidine metabolism – 5C50.3 Disorders of tryptophan metabolism – 5C50.4 Disorders of lysine or hydroxylysine metabolism – 5C50.5 Disorders of the gamma-glutamyl cycle – 5C50.6 Disorders of serine metabolism – 5C50.7 Disorders of glycine metabolism – 5C50.8 Disorders of proline or hydroxyproline metabolism – 5C50.9 Disorders of ornithine metabolism – 5C50.A Disorders of urea cycle metabolism – 5C50.B Disorders of methionine cycle or sulphur amino acid metabolism – 5C50.C Disorders of beta or omega amino acid metabolism – 5C50.D Disorders of branched-chain amino acid metabolism – 5C50.E Organic aciduria – 5C50.F Disorders of peptide metabolism – 5C50.G Trimethylaminuria – 5C50.Y Other specified inborn errors of amino acid or other organic acid metabolism – 5C50.Z Inborn errors of amino acid or other organic acid metabolism, unspecified –– 5C50.00 Classical phenylketonuria –– 5C50.01 Nonclassical phenylketonuria –– 5C50.02 Embryofetopathy due to maternal phenylketonuria –– 5C50.0Y Other specified phenylketonuria –– 5C50.0Z Phenylketonuria, unspecified –– 5C50.10 Alkaptonuria –– 5C50.11 Tyrosinaemia type 1 –– 5C50.12 Tyrosinaemia type 2 –– 5C50.1Y Other specified disorders of tyrosine metabolism –– 5C50.1Z Disorders of tyrosine metabolism, unspecified –– 5C50.20 Histidinaemia –– 5C50.21 Urocanic aciduria –– 5C50.2Y Other specified disorders of histidine metabolism –– 5C50.2Z Disorders of histidine metabolism, unspecified –– 5C50.70 Glycine encephalopathy –– 5C50.71 Sarcosinaemia –– 5C50.7Y Other specified disorders of glycine metabolism –– 5C50.7Z Disorders of glycine metabolism, unspecified –– 5C50.A0 Argininosuccinic aciduria –– 5C50.A1 Carbamoylphosphate synthetase deficiency –– 5C50.A2 Argininaemia –– 5C50.A3 Citrullinaemia –– 5C50.AY Other specified disorders of urea cycle metabolism –– 5C50.AZ Disorders of urea cycle metabolism, unspecified –– 5C50.D0 Maple-syrup-urine disease –– 5C50.DY Other specified disorders of branched-chain amino acid metabolism –– 5C50.DZ Disorders of branched-chain amino acid metabolism, unspecified –– 5C50.E0 Classical organic aciduria –– 5C50.E1 Cerebral organic aciduria –– 5C50.EY Other specified organic aciduria –– 5C50.EZ Organic aciduria, unspecified –– 5C50.F0 Prolidase deficiency –– 5C50.F1 Carnosinaemia –– 5C50.F2 Homocarnosinosis –– 5C50.FY Other specified disorders of peptide metabolism –– 5C50.FZ Disorders of peptide metabolism, unspecified 5C51 Inborn errors of carbohydrate metabolism – 5C51.0 Disorders of the pentose phosphate pathway – 5C51.1 Disorders of glycerol metabolism – 5C51.2 Disorders of glyoxylate metabolism – 5C51.3 Glycogen storage disease – 5C51.4 Disorders of galactose metabolism – 5C51.5 Disorders of fructose metabolism – 5C51.Y Other specified inborn errors of carbohydrate metabolism – 5C51.Z Inborn errors of carbohydrate metabolism, unspecified –– 5C51.20 Primary hyperoxaluria type 1 –– 5C51.2Y Other specified disorders of glyoxylate metabolism –– 5C51.2Z Disorders of glyoxylate metabolism, unspecified –– 5C51.40 Galactose-1-phosphate uridyltransferase deficiency –– 5C51.41 Galactokinase deficiency –– 5C51.42 Glucose or galactose intolerance of newborn –– 5C51.4Y Other specified disorders of galactose metabolism –– 5C51.4Z Disorders of galactose metabolism, unspecified –– 5C51.50 Hereditary fructose intolerance –– 5C51.5Y Other specified disorders of fructose metabolism –– 5C51.5Z Disorders of fructose metabolism, unspecified 5C52 Inborn errors of lipid metabolism – 5C52.0 Inborn errors of fatty acid oxidation or ketone body metabolism – 5C52.1 Inborn errors of sterol metabolism – 5C52.2 Neutral lipid storage disease – 5C52.Y Other specified inborn errors of lipid metabolism – 5C52.Z Inborn errors of lipid metabolism, unspecified –– 5C52.00 Disorders of carnitine transport or the carnitine cycle –– 5C52.01 Disorders of mitochondrial fatty acid oxidation –– 5C52.02 Disorders of ketone body metabolism –– 5C52.03 Sjögren-Larsson syndrome –– 5C52.0Y Other specified inborn errors of fatty acid oxidation or ketone body metabolism –– 5C52.0Z Inborn errors of fatty acid oxidation or ketone body metabolism, unspecified –– 5C52.10 Disorders of cholesterol synthesis –– 5C52.11 Bile acid synthesis defect with cholestasis –– 5C52.1Y Other specified inborn errors of sterol metabolism –– 5C52.1Z Inborn errors of sterol metabolism, unspecified 5C53 Inborn errors of energy metabolism – 5C53.0 Disorders of pyruvate metabolism – 5C53.1 Disorders of the citric acid cycle – 5C53.2 Disorders of mitochondrial oxidative phosphorylation – 5C53.3 Disorders of mitochondrial membrane transport – 5C53.4 Disorders of creatine metabolism – 5C53.Y Other specified inborn errors of energy metabolism – 5C53.Z Inborn errors of energy metabolism, unspecified –– 5C53.00 Pyruvate kinase deficiency –– 5C53.01 Lactate dehydrogenase deficiency –– 5C53.02 Pyruvate dehydrogenase complex deficiency –– 5C53.03 Pyruvate carboxylase deficiency –– 5C53.0Y Other specified disorders of pyruvate metabolism –– 5C53.0Z Disorders of pyruvate metabolism, unspecified –– 5C53.20 Mitochondrial DNA depletion syndromes –– 5C53.21 Multiple mitochondrial DNA deletion syndromes –– 5C53.22 Coenzyme Q10 deficiency –– 5C53.23 Mitochondrial protein translation defects –– 5C53.24 Leigh syndrome –– 5C53.25 Isolated ATP synthase deficiency –– 5C53.2Y Other specified disorders of mitochondrial oxidative phosphorylation –– 5C53.2Z Disorders of mitochondrial oxidative phosphorylation, unspecified –– 5C53.30 Mitochondrial substrate carrier disorders –– 5C53.31 Mitochondrial protein import disorders –– 5C53.3Y Other specified disorders of mitochondrial membrane transport –– 5C53.3Z Disorders of mitochondrial membrane transport, unspecified 5C54 Inborn errors of glycosylation or other specified protein modification – 5C54.0 Disorders of protein N-glycosylation – 5C54.1 Disorders of protein O-glycosylation – 5C54.2 Disorders of multiple glycosylation or other pathways – 5C54.Y Other specified congenital disorders of glycosylation and protein modification – 5C54.Z Congenital disorders of glycosylation and protein modification, unspecified 5C55 Inborn errors of purine, pyrimidine or nucleotide metabolism – 5C55.0 Disorders of purine metabolism – 5C55.1 Disorders of pyrimidine metabolism – 5C55.2 Disorders of nucleotide metabolism – 5C55.Y Other specified inborn errors of purine, pyrimidine or nucleotide metabolism – 5C55.Z Inborn errors of purine, pyrimidine or nucleotide metabolism, unspecified –– 5C55.00 Xanthinuria –– 5C55.01 Lesch-Nyhan syndrome –– 5C55.0Y Other specified disorders of purine metabolism –– 5C55.0Z Disorders of purine metabolism, unspecified 5C56 Lysosomal diseases – 5C56.0 Sphingolipidosis – 5C56.1 Neuronal ceroid lipofuscinosis – 5C56.2 Glycoproteinosis – 5C56.3 Mucopolysaccharidosis – 5C56.4 Disorders of sialic acid metabolism – 5C56.Y Other specified lysosomal diseases – 5C56.Z Lysosomal diseases, unspecified –– 5C56.00 Gangliosidosis –– 5C56.01 Fabry disease –– 5C56.02 Metachromatic leukodystrophy –– 5C56.0Y Other specified sphingolipidosis –– 5C56.0Z Sphingolipidosis, unspecified –– 5C56.20 Mucolipidosis –– 5C56.21 Oligosaccharidosis –– 5C56.2Y Other specified glycoproteinosis –– 5C56.2Z Glycoproteinosis, unspecified –– 5C56.30 Mucopolysaccharidosis type 1 –– 5C56.31 Mucopolysaccharidosis type 2 –– 5C56.32 Mucopolysaccharidosis type 4 –– 5C56.33 Mucopolysaccharidosis type 6 –– 5C56.3Y Other specified mucopolysaccharidosis –– 5C56.3Z Mucopolysaccharidosis, unspecified 5C57 Peroxisomal diseases – 5C57.0 Disorders of peroxisome biogenesis – 5C57.1 Disorders of peroxisomal alpha-, beta- or omega-oxidation – 5C57.Y Other specified peroxisomal diseases – 5C57.Z Peroxisomal diseases, unspecified 5C58 Inborn errors of porphyrin or heme metabolism – 5C58.0 Disorders of bilirubin metabolism or excretion – 5C58.1 Porphyrias – 5C58.Y Other specified inborn errors of porphyrin or heme metabolism – 5C58.Z Inborn errors of porphyrin or heme metabolism, unspecified –– 5C58.00 Crigler-Najjar syndrome –– 5C58.01 Gilbert syndrome –– 5C58.02 Dubin-Johnson syndrome –– 5C58.03 Progressive familial intrahepatic cholestasis –– 5C58.04 Benign recurrent intrahepatic cholestasis –– 5C58.0Y Other specified disorders of bilirubin metabolism or excretion –– 5C58.0Z Disorders of bilirubin metabolism or excretion, unspecified –– 5C58.10 Porphyria cutanea tarda –– 5C58.12 Erythropoietic porphyrias –– 5C58.13 Variegate porphyria –– 5C58.1Y Other specified porphyrias –– 5C58.1Z Porphyrias, unspecified 5C59 Inborn errors of neurotransmitter metabolism – 5C59.0 Disorders of biogenic amine metabolism – 5C59.1 Disorders of gamma aminobutyric acid metabolism – 5C59.2 Disorders of pyridoxine metabolism – 5C59.Y Other specified inborn errors of neurotransmitter metabolism – 5C59.Z Inborn errors of neurotransmitter metabolism, unspecified –– 5C59.00 Disorders of catecholamine synthesis –– 5C59.01 Disorders of pterin metabolism –– 5C59.0Y Other specified disorders of biogenic amine metabolism –– 5C59.0Z Disorders of biogenic amine metabolism, unspecified 5C5A Alpha-1-antitrypsin deficiency 5C5Y Other specified inborn errors of metabolism 5C5Z Inborn errors of metabolism, unspecified 5C60 Disorders of amino acid absorption or transport – 5C60.0 Oculocerebrorenal syndrome – 5C60.1 Cystinosis – 5C60.2 Cystinuria – 5C60.Y Other specified disorders of amino acid absorption or transport – 5C60.Z Disorders of amino acid absorption or transport, unspecified 5C61 Disorders of carbohydrate absorption or transport – 5C61.0 Glucose-galactose malabsorption – 5C61.1 Maltase-glucoamylase deficiency – 5C61.2 Congenital sucrase-isomaltase deficiency – 5C61.3 Alpha, alpha trehalase deficiency – 5C61.4 Acquired monosaccharide malabsorption – 5C61.5 Disorders of facilitated glucose transport – 5C61.6 Lactose intolerance – 5C61.Y Other specified disorders of carbohydrate absorption or transport – 5C61.Z Disorders of carbohydrate absorption or transport, unspecified –– 5C61.40 Fructose malabsorption –– 5C61.4Y Other specified acquired monosaccharide malabsorption –– 5C61.4Z Acquired monosaccharide malabsorption, unspecified –– 5C61.60 Primary lactase deficiency –– 5C61.61 Congenital lactase deficiency –– 5C61.62 Secondary lactase deficiency –– 5C61.6Z Lactose intolerance, unspecified 5C62 Disorders of lipid absorption or transport 5C63 Disorders of vitamin or non-protein cofactor absorption or transport – 5C63.0 Disorders of cobalamin metabolism or transport – 5C63.1 Disorders of folate metabolism or transport – 5C63.2 Disorders of vitamin D metabolism or transport – 5C63.Y Other specified disorders of vitamin or non-protein cofactor absorption or transport – 5C63.Z Disorders of vitamin or non-protein cofactor absorption or transport, unspecified –– 5C63.20 Hypocalcaemic vitamin D dependent rickets –– 5C63.21 Hypocalcaemic vitamin D resistant rickets –– 5C63.22 Hypophosphataemic rickets –– 5C63.2Y Other specified disorders of vitamin D metabolism or transport –– 5C63.2Z Disorders of vitamin D metabolism or transport, unspecified 5C64 Disorders of mineral absorption or transport – 5C64.0 Disorders of copper metabolism – 5C64.1 Disorders of iron metabolism – 5C64.2 Disorders of zinc metabolism – 5C64.3 Disorders of phosphorus metabolism or phosphatases – 5C64.4 Disorders of magnesium metabolism – 5C64.5 Disorders of calcium metabolism – 5C64.6 Disorders of sodium metabolism – 5C64.7 Disorders of chloride metabolism – 5C64.Y Disorders of other specified mineral absorption and transport – 5C64.Z Disorders of mineral absorption or transport, unspecified –– 5C64.00 Wilson disease –– 5C64.0Y Other specified disorders of copper metabolism –– 5C64.0Z Disorders of copper metabolism, unspecified –– 5C64.10 Iron overload diseases –– 5C64.1Y Other specified disorders of iron metabolism –– 5C64.1Z Disorders of iron metabolism, unspecified –– 5C64.20 Acrodermatitis enteropathica –– 5C64.21 Zinc deficiency syndromes –– 5C64.2Y Other specified disorders of zinc metabolism –– 5C64.2Z Disorders of zinc metabolism, unspecified –– 5C64.40 Hypermagnesaemia –– 5C64.41 Hypomagnesaemia –– 5C64.4Z Disorders of magnesium metabolism, unspecified 5C6Y Other specified disorders of metabolite absorption or transport 5C6Z Disorders of metabolite absorption or transport, unspecified 5C70 Volume depletion – 5C70.0 Dehydration – 5C70.1 Hypovolaemia – 5C70.Y Other specified volume depletion – 5C70.Z Volume depletion, unspecified 5C71 Hyperosmolality or hypernatraemia 5C72 Hypo-osmolality or hyponatraemia 5C73 Acidosis – 5C73.0 Acute respiratory acidosis – 5C73.1 Chronic respiratory acidosis – 5C73.2 Anion gap metabolic acidosis – 5C73.Y Other specified acidosis – 5C73.Z Acidosis, unspecified 5C74 Alkalosis 5C75 Mixed disorder of acid-base balance 5C76 Hyperkalaemia 5C77 Hypokalaemia 5C78 Fluid overload 5C7Y Other specified disorders of fluid, electrolyte or acid-base balance 5C7Z Disorders of fluid, electrolyte or acid-base balance, unspecified 5C80 Hyperlipoproteinaemia – 5C80.0 Hypercholesterolaemia – 5C80.1 Hypertriglyceridaemia – 5C80.2 Mixed hyperlipidaemia – 5C80.3 Hyperalphalipoproteinaemia – 5C80.Y Other specified hyperlipoproteinaemia – 5C80.Z Hyperlipoproteinaemia, unspecified –– 5C80.00 Primary hypercholesterolaemia –– 5C80.01 Secondary hypercholesterolaemia –– 5C80.0Z Hypercholesterolaemia, unspecified 5C81 Hypolipoproteinaemia – 5C81.0 Hypoalphalipoproteinaemia – 5C81.1 Hypobetalipoproteinaemia – 5C81.Y Other specified hypolipoproteinaemia – 5C81.Z Hypolipoproteinaemia, unspecified 5C8Y Other specified disorders of lipoprotein metabolism or lipidaemias 5C8Z Unspecified disorders of lipoprotein metabolism or lipidaemias 5C90 Metabolic or transporter liver disease 5C90.0 Liver diseases due to urea cycle defects 5C90.1 Liver diseases due to disorders of porphyrin or bilirubin metabolism or transport 5C90.2 Liver diseases due to disorders of amino acid metabolism 5C90.3 Liver disease due to disorders of lysosomal storage 5C90.4 Liver diseases due to mitochondrial disorders 5C90.5 Liver diseases due to disorders of mineral metabolism 5C90.Y Other specified metabolic or transporter liver disease 5C90.Z Metabolic or transporter liver disease, unspecified 5D00 Amyloidosis – 5D00.0 AL amyloidosis – 5D00.1 AA amyloidosis – 5D00.2 Hereditary amyloidosis – 5D00.3 Dialysis-associated amyloidosis – 5D00.Y Other specified amyloidosis – 5D00.Z Amyloidosis, unspecified –– 5D00.20 Hereditary ATTR amyloidosis –– 5D00.21 Non-neuropathic heredofamilial amyloidosis –– 5D00.2Y Other specified hereditary amyloidosis –– 5D00.2Z Hereditary amyloidosis, unspecified 5D01 Tumour lysis syndrome 5D0Y Other specified metabolic disorders 5D2Z Metabolic disorders, unspecified 5D40 Postprocedural hypothyroidism 5D40.0 Postirridation hypothyroidism 5D40.Y Other specified postprocedural hypothyroidism 5D40.Z Postprocedural hypothyroidism, unspecified – 5D40.00 Hypothyroidism postradioactive iodine ablation – 5D40.0Y Other specified postirridation hypothyroidism – 5D40.0Z Postirridation hypothyroidism, unspecified 5D41 Postprocedural hypoinsulinaemia 5D42 Postprocedural hypoparathyroidism 5D43 Postprocedural hypopituitarism 5D44 Postprocedural ovarian failure 5D45 Postprocedural testicular hypofunction 5D46 Postprocedural adrenocortical hypofunction
synonyms Endocrine, nutritional or metabolic diseases complicating pregnancy, childbirth or the puerperium
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