Unlock the full potential of your medical coding capabilities with the CPT® Advanced Coding Pack from the American Medical Association (AMA). Designed for professional medical coders, auditors, and billers like you, this comprehensive suite of resources provides everything you need to navigate the complexities of the CPT code set with confidence and precision.
Advanced Coding Pack includes:
CPT Assistant - Newsletter with official education and guidance
CPT Knowledge Base - Commonly asked coding questions answered by the experts
CPT Vignettes - Comprehensive clinical examples.
Add to your Find-A-Code subscription for $300 / person
Learn More and Subscribe
GA20.01 Secondary amenorrhoea International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01 In women who have menstruated previously, no menses for an interval of time equivalent to a total of at least 3 previous cycles, or 6 months
postcoordination Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
Has causing condition - a selection is required - 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 GA00 Vulvitis – GA00.0 Acute vulvitis – GA00.1 Subacute, chronic or recurrent vulvitis – GA00.2 Abscess of vulva – GA00.3 Genital ulcer of vulva – GA00.4 Vulvovaginal ulceration and inflammation –– GA00.40 Vulvovaginal ulceration –– GA00.4Y Other specified vulvovaginal ulceration and inflammation –– GA00.4Z Vulvovaginal ulceration and inflammation, unspecified GA01 Inflammatory disorders of the uterus, except cervix – GA01.0 Acute inflammatory disease of uterus – GA01.1 Chronic inflammatory disease of uterus – GA01.Y Other specified inflammatory disorders of the uterus, except cervix – GA01.Z Inflammatory disorders of the uterus, except cervix, unspecified –– GA01.00 Acute endometritis –– GA01.01 Acute inflammatory disease of uterus with pyometra –– GA01.0Z Acute inflammatory disease of uterus, unspecified –– GA01.10 Chronic endometritis –– GA01.11 Chronic inflammatory disease of uterus with pyometra –– GA01.1Z Chronic inflammatory disease of uterus, unspecified GA02 Vaginitis – GA02.0 Acute vaginitis – GA02.1 Inflammatory vaginitis – GA02.2 Subacute or chronic vaginitis – GA02.3 Genital ulcer disease of vagina – GA02.Z Vaginitis, unspecified GA03 Diseases of Bartholin gland – GA03.0 Abscess of Bartholin gland – GA03.1 Cyst of Bartholin gland – GA03.Y Other specified diseases of Bartholin gland – GA03.Z Diseases of Bartholin gland, unspecified GA04 Cervicitis GA05 Female pelvic inflammatory diseases – GA05.0 Acute female pelvic inflammatory disease – GA05.1 Chronic pelvic inflammatory disease – GA05.2 Female pelvic peritonitis, unspecified – GA05.3 Tuboovarian abscess – GA05.Y Other specified female pelvic inflammatory diseases – GA05.Z Female pelvic inflammatory diseases, unspecified GA06 Pelvic peritoneal adhesions of unknown or combined origin GA07 Salpingitis and oophoritis – GA07.0 Acute salpingitis and oophoritis – GA07.1 Chronic salpingitis and oophoritis – GA07.Z Salpingitis and oophoritis, unspecified GA0Z Inflammatory disorders of the female genital tract, unspecified GA12 Dyspareunia GA13 Acquired abnormalities of vulva or perineum – GA13.0 Polyp of vulva – GA13.1 Low grade squamous intraepithelial lesion of vulva – GA13.2 Hypertrophy of vulva – GA13.3 Vulvar cyst – GA13.4 Labial agglutination – GA13.5 Skene duct cyst – GA13.6 Vulvar laceration – GA13.7 Vulvar haematoma – GA13.Y Other specified acquired abnormalities of vulva or perineum – GA13.Z Acquired abnormalities of vulva or perineum, unspecified GA14 Acquired abnormalities of vagina – GA14.0 Polyp of vagina – GA14.1 Haematocolpos – GA14.2 Vaginal foreign body – GA14.3 Vaginal haematoma – GA14.5 Leukoplakia of vagina – GA14.6 Low grade squamous intraepithelial lesion of vagina – GA14.Y Other specified acquired abnormalities of vagina – GA14.Z Acquired abnormalities of vagina, unspecified GA15 Acquired abnormalities of cervix uteri – GA15.0 Polyp of cervix uteri – GA15.1 Erosion or ectropion of cervix uteri – GA15.2 Nabothian cyst – GA15.3 Old laceration of cervix uteri – GA15.4 Stricture or stenosis of cervix uteri – GA15.5 Hypertrophic elongation of cervix uteri – GA15.6 Incompetence of cervix uteri – GA15.7 Low grade squamous intraepithelial lesion of cervix uteri – GA15.Y Other specified acquired abnormalities of cervix uteri – GA15.Z Acquired abnormalities of cervix uteri, unspecified GA16 Acquired abnormalities of uterus, except cervix – GA16.0 Endometrial glandular hyperplasia – GA16.1 Malposition of uterus – GA16.2 Intrauterine synechiae – GA16.3 Haematometra – GA16.Y Other specified acquired abnormalities of uterus, except cervix – GA16.Z Acquired abnormalities of uterus, except cervix, unspecified GA17 Acquired abnormalities of fallopian tube – GA17.0 Acquired parafimbrial cyst of the fallopian tube – GA17.1 Fimbrial agglutination – GA17.2 Hydrosalpinx – GA17.3 Haematosalpinx – GA17.4 Salpingitis isthmica nodosa – GA17.Y Other specified acquired abnormalities of fallopian tube – GA17.Z Acquired abnormalities of fallopian tube, unspecified GA18 Acquired abnormalities of ovary – GA18.0 Follicular cyst of ovary – GA18.1 Corpus luteum cyst – GA18.2 Theca lutein cyst – GA18.4 Para ovarian cyst – GA18.5 Torsion of ovary, ovarian pedicle or fallopian tube – GA18.6 Other or unspecified ovarian cysts – GA18.7 Acquired atrophy of ovary or fallopian tube – GA18.Y Other specified acquired abnormalities of ovary – GA18.Z Acquired abnormalities of ovary, unspecified GA19 Acquired abnormalities of broad ligament – GA19.0 Haematoma of broad ligament – GA19.Y Other specified acquired abnormalities of broad ligament – GA19.Z Acquired abnormalities of broad ligament, unspecified GA1Y Other specified noninflammatory disorders of female genital tract GA1Z Noninflammatory disorders of female genital tract, unspecified GA30 Menopausal or certain specified perimenopausal disorders GA30.0 Menopause GA30.1 Postmenopausal uterine bleeding GA30.2 Postmenopausal atrophic vaginitis GA30.3 States associated with artificial menopause GA30.4 Menopausal hot flush GA30.5 Menopausal osteoporosis GA30.6 Premature ovarian failure GA30.Y Other specified menopausal and perimenopausal disorders GA30.Z Menopausal and perimenopausal disorders, unspecified – GA30.00 Menopausal or female climacteric states – GA30.01 Menopausal transition – GA30.02 Excessive bleeding in the premenopausal period – GA30.0Y Other specified menopause – GA30.0Z Menopause, unspecified GA31 Female infertility GA31.0 Primary female infertility GA31.1 Secondary female infertility GA31.Z Female infertility without specification whether primary or secondary – GA31.00 Primary female infertility of uterine origin – GA31.01 Primary female infertility of tubal origin – GA31.0Y Primary female infertility of other specified origin – GA31.0Z Primary female infertility of unspecified origin – GA31.10 Secondary female infertility of uterine origin – GA31.11 Secondary female infertility of tubal origin – GA31.1Y Secondary female infertility of other specified origin – GA31.1Z Secondary female infertility of unspecified origin GA32 Complications associated with medically assisted reproduction GA32.0 Ovarian hyperstimulation syndrome GA32.1 Bleeding after egg retrieval GA32.2 Infection associated with medically assisted reproduction GA32.3 Complications of attempted embryo transfer or medically assisted insemination GA32.Y Other specified complications associated with medically assisted reproduction GA32.Z Complications associated with medically assisted reproduction, unspecified GA33 Recurrent pregnancy loss GA34 Female pelvic pain associated with genital organs or menstrual cycle GA34.0 Pain related to vulva, vagina or pelvic floor GA34.1 Vaginal laxity GA34.2 Female pelvic pain GA34.3 Dysmenorrhoea GA34.4 Premenstrual disturbances GA34.5 Ovarian remnant syndrome GA34.6 Female genital pain GA34.Y Other specified female pelvic pain associated with genital organs or menstrual cycle GA34.Z Female pelvic pain associated with genital organs or menstrual cycle, unspecified – GA34.00 Vulval pain – GA34.01 Perineal pain – GA34.02 Vulvodynia – GA34.0Y Other specified pain related to vulva, vagina or pelvic floor – GA34.0Z Pain related to vulva, vagina or pelvic floor, unspecified – GA34.20 Cyclic pelvic pain – GA34.21 Noncyclic pelvic pain – GA34.2Z Female pelvic pain, unspecified – GA34.40 Premenstrual tension syndrome – GA34.41 Premenstrual dysphoric disorder – GA34.4Y Other specified premenstrual disturbances – GA34.4Z Premenstrual disturbances, unspecified LA00 Anencephaly or similar anomalies – LA00.0 Anencephaly – LA00.1 Iniencephaly – LA00.2 Acephaly – LA00.3 Amyelencephaly – LA00.Y Other specified anencephaly or similar anomalies – LA00.Z Anencephaly or similar anomalies, unspecified –– LA00.00 Craniorachischisis –– LA00.0Y Other specified anencephaly –– LA00.0Z Anencephaly, unspecified LA01 Cephalocele LA02 Spina bifida – LA02.0 Spina bifida cystica – LA02.1 Spina bifida aperta – LA02.Y Other specified spina bifida – LA02.Z Spina bifida, unspecified –– LA02.00 Myelomeningocele with hydrocephalus –– LA02.01 Myelomeningocele without hydrocephalus –– LA02.02 Myelocystocele –– LA02.0Y Other specified spina bifida cystica –– LA02.0Z Spina bifida cystica, unspecified LA03 Arnold-Chiari malformation type II LA04 Congenital hydrocephalus – LA04.0 Hydrocephalus with stenosis of the aqueduct of Sylvius – LA04.Y Other specified congenital hydrocephalus – LA04.Z Congenital hydrocephalus, unspecified LA05 Cerebral structural developmental anomalies – LA05.0 Microcephaly – LA05.1 Megalencephaly – LA05.2 Holoprosencephaly – LA05.3 Corpus callosum agenesis – LA05.4 Arrhinencephaly – LA05.5 Abnormal neuronal migration – LA05.6 Encephaloclastic disorders – LA05.7 Brain cystic malformations – LA05.8 Colpocephaly – LA05.Y Other specified cerebral structural developmental anomalies – LA05.Z Cerebral structural developmental anomalies, unspecified –– LA05.50 Polymicrogyria –– LA05.51 Cortical dysplasia –– LA05.5Y Other specified abnormal neuronal migration –– LA05.5Z Abnormal neuronal migration, unspecified –– LA05.60 Porencephaly –– LA05.61 Schizencephaly –– LA05.62 Hydranencephaly –– LA05.6Y Other specified encephaloclastic disorders –– LA05.6Z Encephaloclastic disorders, unspecified LA06 Cerebellar structural developmental anomalies – LA06.0 Dandy-Walker malformation – LA06.1 Hypoplasia or agenesis of cerebellar hemispheres – LA06.2 Focal cerebellar dysplasia – LA06.Y Other specified cerebellar structural developmental anomalies – LA06.Z Cerebellar structural developmental anomalies, unspecified LA07 Structural developmental anomalies of the neurenteric canal, spinal cord or vertebral column – LA07.0 Primary tethered cord syndrome – LA07.1 Diastematomyelia – LA07.2 Amyelia – LA07.3 Primary syringomyelia or hydromyelia – LA07.4 Arnold-Chiari malformation type I – LA07.Y Other specified structural developmental anomalies of the neurenteric canal, spinal cord or vertebral column – LA07.Z Structural developmental anomalies of the neurenteric canal, spinal cord or vertebral column, unspecified LA0Y Other specified structural developmental anomalies of the nervous system LA0Z Structural developmental anomalies of the nervous system, unspecified LA10 Structural developmental anomalies of ocular globes – LA10.0 Microphthalmos – LA10.1 Clinical anophthalmos – LA10.2 Buphthalmos – LA10.3 Congenital macrophthalmos – LA10.Y Other specified structural developmental anomalies of ocular globes – LA10.Z Structural developmental anomalies of ocular globes, unspecified LA11 Structural developmental anomalies of the anterior segment of eye – LA11.0 Blue sclera – LA11.1 Structural developmental anomalies of cornea – LA11.2 Anterior segment dysgenesis – LA11.3 Aniridia – LA11.4 Coloboma of iris – LA11.5 Congenital corneal opacity – LA11.6 Structural disorders of the pupil – LA11.Y Other specified structural developmental anomalies of the anterior segment of eye – LA11.Z Structural developmental anomalies of the anterior segment of eye, unspecified –– LA11.60 Irregular pupil of the eye –– LA11.61 Iridoschisis –– LA11.62 Anomalies of pupillary function –– LA11.6Y Other specified structural disorders of the pupil –– LA11.6Z Structural disorders of the pupil, unspecified LA12 Structural developmental anomalies of lens or zonula – LA12.0 Coloboma of lens – LA12.1 Congenital cataract – LA12.2 Congenital aphakia – LA12.3 Spherophakia – LA12.Y Other specified structural developmental anomalies of lens or zonula – LA12.Z Structural developmental anomalies of lens or zonula, unspecified LA13 Structural developmental anomalies of the posterior segment of eye – LA13.0 Congenital anomalies of the vitreous – LA13.1 Coloboma of choroid or retina – LA13.2 Coloboma of macula – LA13.3 Congenital vitreoretinal dysplasia – LA13.5 Congenital retinal aneurysm – LA13.6 Congenital malformations of choroid – LA13.7 Congenital malformation of optic disc – LA13.8 Certain congenital malformations of posterior segment of eye – LA13.Y Other specified structural developmental anomalies of the posterior segment of eye – LA13.Z Structural developmental anomalies of the posterior segment of eye, unspecified –– LA13.70 Isolated optic nerve hypoplasia –– LA13.71 Optic nerve aplasia –– LA13.72 Congenitally elevated optic disc –– LA13.73 Optic disc dysplasia –– LA13.74 Megalopapilla –– LA13.76 Coloboma of optic disc –– LA13.7Y Other specified congenital malformation of optic disc –– LA13.7Z Congenital malformation of optic disc, unspecified –– LA13.80 Anastomosis of retinal or choroidal vessels LA14 Structural developmental anomalies of eyelid, lacrimal apparatus or orbit – LA14.0 Structural developmental anomalies of eyelids – LA14.1 Structural developmental anomalies of lacrimal apparatus – LA14.2 Structural developmental anomalies of orbit – LA14.Y Other specified structural developmental anomalies of eyelid, lacrimal apparatus or orbit – LA14.Z Structural developmental anomalies of eyelid, lacrimal apparatus or orbit, unspecified –– LA14.00 Palpebral cleft or coloboma –– LA14.01 Cryptophthalmia –– LA14.02 Congenital entropion –– LA14.03 Congenital ectropion –– LA14.04 Congenital ptosis –– LA14.05 Congenital eyelid retraction –– LA14.06 Epibulbar choristoma –– LA14.07 Ankyloblepharon filiforme adnatum –– LA14.0Y Other specified structural developmental anomalies of eyelids –– LA14.10 Aplasia of lacrimal or salivary glands –– LA14.11 Agenesis of lacrimal ducts –– LA14.12 Congenital dacryocele –– LA14.13 Congenital agenesis of lacrimal punctum –– LA14.14 Congenital stenosis or stricture of lacrimal duct –– LA14.1Y Other specified structural developmental anomalies of lacrimal apparatus –– LA14.1Z Structural developmental anomalies of lacrimal apparatus, unspecified LA1Y Other specified structural developmental anomalies of the eye, eyelid or lacrimal apparatus LA1Z Structural developmental anomalies of the eye, eyelid or lacrimal apparatus, unspecified LA20 Structural anomaly of eustachian apparatus LA21 Minor anomalies of pinnae – LA21.0 Macrotia – LA21.1 Protruding ear – LA21.2 Low-set ear – LA21.3 Misshapen ear – LA21.Y Other specified minor anomalies of pinnae – LA21.Z Minor anomalies of pinnae, unspecified LA22 Structural developmental anomalies of ear causing hearing impairment – LA22.0 Microtia – LA22.1 Anotia – LA22.2 Aplasia or hypoplasia of external auditory canal – LA22.3 Structural developmental anomalies of ear ossicles – LA22.4 Structural developmental anomalies of inner ear – LA22.Y Other specified structural developmental anomalies of ear causing hearing impairment – LA22.Z Structural developmental anomalies of ear causing hearing impairment, unspecified LA23 Otocephaly LA24 Accessory auricle LA2Y Other specified structural developmental anomalies of the ear LA2Z Structural developmental anomalies of the ear, unspecified LA30 Structural developmental anomalies of teeth and periodontal tissues – LA30.0 Anodontia – LA30.1 Hypodontia – LA30.2 Oligodontia – LA30.3 Hyperdontia – LA30.4 Abnormalities of size or form of teeth – LA30.5 Anomalies in tooth resorption or loss – LA30.6 Amelogenesis imperfecta – LA30.7 Dentine dysplasia – LA30.8 Dentinogenesis imperfecta – LA30.9 Odontogenesis imperfecta – LA30.Y Other specified structural developmental anomalies of teeth and periodontal tissues – LA30.Z Structural developmental anomalies of teeth and periodontal tissues, unspecified –– LA30.50 Early exfoliation of teeth –– LA30.51 Late exfoliation of teeth –– LA30.5Y Other specified anomalies in tooth resorption or loss –– LA30.5Z Anomalies in tooth resorption or loss, unspecified LA31 Structural developmental anomalies of mouth or tongue – LA31.0 Congenital macroglossia – LA31.1 Hypoglossia or aglossia – LA31.2 Ankyloglossia – LA31.3 Macrostomia – LA31.4 Microstomia – LA31.Y Other specified structural developmental anomalies of mouth or tongue – LA31.Z Structural developmental anomalies of mouth or tongue, unspecified – LA40 Cleft lip –– LA40.0 Cleft lip, unilateral –– LA40.1 Cleft lip, bilateral –– LA40.2 Cleft lip, median –– LA40.Z Cleft lip, unspecified – LA41 Cleft lip and alveolus –– LA41.0 Cleft lip and alveolus, unilateral –– LA41.1 Cleft lip and alveolus, bilateral –– LA41.Z Cleft lip and alveolus, unspecified – LA42 Cleft palate –– LA42.0 Cleft hard palate –– LA42.1 Cleft soft palate –– LA42.2 Cleft uvula –– LA42.Z Cleft palate, unspecified – LA4Y Other specified clefts of lip, alveolus or palate – LA4Z Clefts of lip, alveolus or palate, unspecified LA50 Congenital velopharyngeal incompetence LA51 Facial clefts LA52 Facial asymmetry LA53 Macrocheilia LA54 Microcheilia LA55 Compression facies LA56 Pierre Robin syndrome LA5Y Other specified structural developmental anomalies of the face LA5Z Structural developmental anomalies of the face, unspecified LA60 Webbed neck LA61 Congenital sternomastoid tumour LA62 Congenital torticollis LA6Y Other specified structural developmental anomalies of the neck LA6Z Structural developmental anomalies of the neck, unspecified LA70 Structural developmental anomalies of the nose or cavum – LA70.0 Arrhinia – LA70.1 Bifid nose – LA70.2 Choanal atresia – LA70.3 Congenital perforated nasal septum – LA70.Y Other specified structural developmental anomalies of the nose or cavum – LA70.Z Structural developmental anomalies of the nose or cavum, unspecified LA71 Structural developmental anomalies of larynx – LA71.0 Congenital laryngomalacia – LA71.1 Laryngocele – LA71.2 Laryngeal hypoplasia – LA71.3 Congenital subglottic stenosis – LA71.Y Other specified structural developmental anomalies of larynx – LA71.Z Structural developmental anomalies of larynx, unspecified LA72 Laryngotracheooesophageal cleft LA73 Structural developmental anomalies of trachea – LA73.0 Congenital stenosis of trachea – LA73.1 Congenital tracheomalacia – LA73.Y Other specified structural developmental anomalies of trachea – LA73.Z Structural developmental anomalies of trachea, unspecified LA74 Structural developmental anomalies of bronchi – LA74.0 Congenital stenosis or atresia of bronchus – LA74.1 Congenital bronchomalacia – LA74.Y Other specified structural developmental anomalies of bronchi – LA74.Z Structural developmental anomalies of bronchi, unspecified LA75 Structural developmental anomalies of lungs – LA75.0 Accessory lobe of lung – LA75.1 Agenesis of lung – LA75.2 Congenital hypoplasia of lung – LA75.3 Congenital hyperplasia of lung – LA75.4 Congenital pulmonary airway malformations – LA75.5 Congenital lobar emphysema – LA75.6 Congenital sequestration of lung – LA75.Y Other specified structural developmental anomalies of lungs – LA75.Z Structural developmental anomalies of lungs, unspecified LA76 Structural developmental anomalies of pleura LA77 Congenital cyst of mediastinum LA7Y Other specified structural developmental anomalies of the respiratory system LA7Z Structural developmental anomalies of the respiratory system, unspecified – LA80 Anomalous position-orientation of heart –– LA80.0 Laevocardia –– LA80.1 Dextrocardia –– LA80.2 Mesocardia –– LA80.3 Extrathoracic heart –– LA80.Y Other specified anomalous position-orientation of heart –– LA80.Z Anomalous position-orientation of heart, unspecified – LA81 Abnormal ventricular relationships – LA82 Total mirror imagery – LA83 Right isomerism – LA84 Left isomerism – LA85 Congenital anomaly of an atrioventricular or ventriculo-arterial connection –– LA85.0 Discordant atrioventricular connections –– LA85.1 Transposition of the great arteries –– LA85.2 Double outlet right ventricle –– LA85.3 Double outlet left ventricle –– LA85.4 Common arterial trunk –– LA85.Y Other specified congenital anomaly of an atrioventricular or ventriculo-arterial connection –– LA85.Z Congenital anomaly of an atrioventricular or ventriculo-arterial connection, unspecified ––– LA85.00 Congenitally corrected transposition of great arteries ––– LA85.0Y Other specified discordant atrioventricular connections ––– LA85.0Z Discordant atrioventricular connections, unspecified ––– LA85.20 Double outlet right ventricle with subpulmonary ventricular septal defect, transposition type ––– LA85.21 Double outlet right ventricle with non-committed ventricular septal defect ––– LA85.22 Double outlet right ventricle with subaortic or doubly committed ventricular septal defect without pulmonary stenosis, ventricular septal defect type ––– LA85.23 Double outlet right ventricle with subaortic or doubly committed ventricular septal defect and pulmonary stenosis, Fallot type ––– LA85.2Y Other specified double outlet right ventricle ––– LA85.2Z Double outlet right ventricle, unspecified ––– LA85.40 Common arterial trunk with aortic dominance ––– LA85.41 Common arterial trunk with pulmonary dominance and interrupted aortic arch ––– LA85.4Y Other specified common arterial trunk ––– LA85.4Z Common arterial trunk, unspecified – LA86 Congenital anomaly of mediastinal vein –– LA86.0 Left superior caval vein –– LA86.1 Unroofed coronary sinus –– LA86.2 Anomalous pulmonary venous connection –– LA86.3 Congenital pulmonary venous stenosis or hypoplasia –– LA86.Y Other specified congenital anomaly of mediastinal vein –– LA86.Z Congenital anomaly of mediastinal vein, unspecified ––– LA86.20 Total anomalous pulmonary venous connection ––– LA86.21 Partial anomalous pulmonary venous connection ––– LA86.22 Scimitar syndrome ––– LA86.2Y Other specified anomalous pulmonary venous connection ––– LA86.2Z Anomalous pulmonary venous connection, unspecified – LA87 Congenital anomaly of an atrioventricular valve or atrioventricular septum –– LA87.0 Congenital anomaly of tricuspid valve –– LA87.1 Congenital anomaly of mitral valve –– LA87.3 Common atrioventricular junction without an atrioventricular septal defect –– LA87.4 Common atrioventricular junction with atrioventricular septal defect –– LA87.Y Other specified congenital anomaly of an atrioventricular valve or atrioventricular septum –– LA87.Z Congenital anomaly of an atrioventricular valve or atrioventricular septum, unspecified ––– LA87.00 Congenital tricuspid regurgitation ––– LA87.01 Congenital tricuspid valvar stenosis ––– LA87.02 Dysplasia of tricuspid valve ––– LA87.03 Ebstein malformation of tricuspid valve ––– LA87.0Y Other specified congenital anomaly of tricuspid valve ––– LA87.0Z Congenital anomaly of tricuspid valve, unspecified ––– LA87.10 Congenital mitral regurgitation ––– LA87.11 Congenital mitral valvar stenosis ––– LA87.12 Dysplasia of mitral valve ––– LA87.13 Congenital anomaly of mitral subvalvar apparatus ––– LA87.1Y Other specified congenital anomaly of mitral valve ––– LA87.1Z Congenital anomaly of mitral valve, unspecified ––– LA87.40 Atrioventricular septal defect with communication at the atrial level only ––– LA87.41 Atrioventricular septal defect with communication at the ventricular level only ––– LA87.42 Atrioventricular septal defect with communication at atrial level and restrictive communication at ventricular level ––– LA87.43 Atrioventricular septal defect with communication at atrial level and unrestrictive communication at ventricular level ––– LA87.44 Atrioventricular septal defect with ventricular imbalance ––– LA87.45 Atrioventricular septal defect and tetralogy of Fallot ––– LA87.4Y Other specified common atrioventricular junction with atrioventricular septal defect ––– LA87.4Z Common atrioventricular junction with atrioventricular septal defect, unspecified – LA88 Congenital anomaly of a ventricle or the ventricular septum –– LA88.0 Congenital right ventricular outflow tract obstruction –– LA88.1 Double chambered right ventricle –– LA88.2 Tetralogy of Fallot –– LA88.3 Congenital left ventricular outflow tract obstruction –– LA88.4 Ventricular septal defect –– LA88.Y Other specified congenital anomaly of a ventricle or the ventricular septum –– LA88.Z Congenital anomaly of a ventricle or the ventricular septum, unspecified ––– LA88.20 Tetralogy of Fallot with absent pulmonary valve syndrome ––– LA88.21 Tetralogy of Fallot with pulmonary atresia ––– LA88.22 Tetralogy of Fallot with pulmonary atresia and systemic-to-pulmonary collateral artery ––– LA88.2Y Other specified tetralogy of Fallot ––– LA88.2Z Tetralogy of Fallot, unspecified ––– LA88.40 Trabecular muscular ventricular septal defect ––– LA88.41 Perimembranous central ventricular septal defect ––– LA88.42 Ventricular septal defect haemodynamically insignificant ––– LA88.4Y Other specified ventricular septal defect ––– LA88.4Z Ventricular septal defect, unspecified – LA89 Functionally univentricular heart –– LA89.0 Double inlet atrioventricular connection –– LA89.1 Tricuspid atresia –– LA89.2 Mitral atresia –– LA89.3 Hypoplastic left heart syndrome –– LA89.Y Other specified functionally univentricular heart –– LA89.Z Functionally univentricular heart, unspecified – LA8A Congenital anomaly of a ventriculo-arterial valve or adjacent regions –– LA8A.0 Congenital anomaly of pulmonary valve –– LA8A.1 Congenital pulmonary atresia –– LA8A.2 Congenital anomaly of aortic valve –– LA8A.3 Congenital supravalvar aortic stenosis –– LA8A.4 Aneurysm of aortic sinus of Valsalva –– LA8A.5 Congenital subaortic stenosis –– LA8A.6 Congenital subpulmonary stenosis –– LA8A.Y Other specified congenital anomaly of a ventriculo-arterial valve or adjacent regions –– LA8A.Z Congenital anomaly of a ventriculo-arterial valve or adjacent regions, unspecified ––– LA8A.00 Congenital pulmonary valvar stenosis ––– LA8A.01 Congenital pulmonary regurgitation ––– LA8A.0Y Other specified congenital anomaly of pulmonary valve ––– LA8A.0Z Congenital anomaly of pulmonary valve, unspecified ––– LA8A.10 Pulmonary atresia with intact ventricular septum ––– LA8A.1Y Other specified congenital pulmonary atresia ––– LA8A.1Z Congenital pulmonary atresia, unspecified ––– LA8A.20 Congenital aortic valvar stenosis ––– LA8A.21 Congenital aortic regurgitation ––– LA8A.22 Bicuspid aortic valve ––– LA8A.23 Aortic valvar atresia ––– LA8A.24 Unicuspid aortic valve ––– LA8A.2Y Other specified congenital anomaly of aortic valve ––– LA8A.2Z Congenital anomaly of aortic valve, unspecified – LA8B Congenital anomaly of great arteries including arterial duct –– LA8B.0 Congenital aortopulmonary window –– LA8B.1 Congenital anomaly of pulmonary arterial tree –– LA8B.2 Congenital anomaly of aorta or its branches –– LA8B.3 Tracheo-oesophageal compressive syndrome –– LA8B.4 Patent arterial duct –– LA8B.Y Other specified congenital anomaly of great arteries including arterial duct –– LA8B.Z Congenital anomaly of great arteries including arterial duct, unspecified ––– LA8B.21 Coarctation of aorta ––– LA8B.22 Interrupted aortic arch ––– LA8B.23 Congenital anomaly of descending thoracic or abdominal aorta ––– LA8B.24 Congenital anomaly of aortic arch branch ––– LA8B.2Y Other specified congenital anomaly of aorta or its branches ––– LA8B.2Z Congenital anomaly of aorta or its branches, unspecified – LA8C Congenital anomaly of coronary artery –– LA8C.0 Anomalous origin of coronary artery from pulmonary arterial tree –– LA8C.1 Anomalous aortic origin or course of coronary artery –– LA8C.2 Congenital coronary arterial fistula –– LA8C.Y Other specified congenital anomaly of coronary artery –– LA8C.Z Congenital anomaly of coronary artery, unspecified – LA8D Congenital pericardial anomaly – LA8E Congenital anomaly of atrial septum –– LA8E.0 Patent oval foramen –– LA8E.1 Atrial septal defect within oval fossa –– LA8E.2 Sinus venosus defect –– LA8E.3 Interatrial communication through coronary sinus orifice –– LA8E.Y Other specified congenital anomaly of atrial septum –– LA8E.Z Congenital anomaly of atrial septum, unspecified – LA8F Congenital anomaly of right atrium – LA8G Congenital anomaly of left atrium –– LA8G.0 Divided left atrium –– LA8G.Y Other specified congenital anomaly of left atrium –– LA8G.Z Congenital anomaly of left atrium, unspecified – LA8Y Other specified structural developmental anomaly of heart or great vessels – LA8Z Structural developmental anomaly of heart or great vessels, unspecified LA90 Structural developmental anomalies of the peripheral vascular system – LA90.0 Capillary malformations – LA90.1 Lymphatic malformations – LA90.2 Peripheral venous malformations – LA90.3 Peripheral arteriovenous malformations – LA90.4 Peripheral arterial malformations – LA90.5 Pulmonary arteriovenous fistula – LA90.Y Other specified structural developmental anomalies of the peripheral vascular system – LA90.Z Structural developmental anomalies of the peripheral vascular system, unspecified –– LA90.00 Hereditary haemorrhagic telangiectasia –– LA90.0Y Other specified capillary malformations –– LA90.0Z Capillary malformations, unspecified –– LA90.10 Macrocystic lymphatic malformation –– LA90.11 Microcystic lymphatic malformation –– LA90.12 Lymphatic malformations of certain specified sites –– LA90.13 Cystic hygroma in fetus –– LA90.1Y Other specified lymphatic malformations –– LA90.1Z Lymphatic malformations, unspecified –– LA90.20 Vein of Galen aneurysm –– LA90.21 Congenital portosystemic shunt –– LA90.2Y Other specified peripheral venous malformations –– LA90.2Z Peripheral venous malformations, unspecified –– LA90.30 Portal vein-hepatic artery fistula –– LA90.31 Arteriovenous malformation of precerebral vessels –– LA90.32 Uterine arteriovenous malformations –– LA90.3Y Other specified peripheral arteriovenous malformations –– LA90.3Z Peripheral arteriovenous malformations, unspecified –– LA90.40 Congenital renal artery stenosis –– LA90.41 Congenital precerebral nonruptured aneurysm –– LA90.42 Congenital cerebral nonruptured aneurysm –– LA90.4Y Other specified peripheral arterial malformations –– LA90.4Z Peripheral arterial malformations, unspecified LA9Y Other specified structural developmental anomalies of the circulatory system LA9Z Structural developmental anomalies of the circulatory system, unspecified LB00 Structural developmental anomalies of diaphragm – LB00.0 Congenital diaphragmatic hernia – LB00.1 Absence of diaphragm – LB00.Y Other specified structural developmental anomalies of diaphragm – LB00.Z Structural developmental anomalies of diaphragm, unspecified LB01 Omphalocele LB02 Gastroschisis LB03 Structural developmental anomalies of umbilical cord – LB03.0 Allantoic duct remnants or cysts – LB03.1 Single umbilical cord artery – LB03.Y Other specified structural developmental anomalies of umbilical cord – LB03.Z Structural developmental anomalies of umbilical cord, unspecified LB0Y Other specified structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord LB0Z Structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord, unspecified LB10 Structural developmental anomalies of salivary glands or ducts LB11 Congenital diverticulum of pharynx LB12 Structural developmental anomalies of oesophagus – LB12.0 Congenital oesophageal web or ring – LB12.1 Atresia of oesophagus – LB12.2 Oesophageal fistula without atresia – LB12.3 Congenital stenosis or stricture of oesophagus – LB12.4 Congenital diverticulum of oesophagus – LB12.5 Congenital dilatation of oesophagus – LB12.Y Other specified structural developmental anomalies of oesophagus – LB12.Z Structural developmental anomalies of oesophagus, unspecified –– LB12.10 Atresia of oesophagus with oesophagobronchial fistula –– LB12.1Y Other specified atresia of oesophagus –– LB12.1Z Atresia of oesophagus, unspecified LB13 Structural developmental anomalies of stomach – LB13.0 Congenital hypertrophic pyloric stenosis – LB13.1 Congenital hiatus hernia – LB13.2 Congenital antral web – LB13.Y Other specified structural developmental anomalies of stomach – LB13.Z Structural developmental anomalies of stomach, unspecified LB14 Structural developmental anomalies of duodenum LB15 Structural developmental anomalies of small intestine – LB15.0 Meckel diverticulum – LB15.1 Atresia of small intestine – LB15.2 Congenital short bowel – LB15.3 Congenital diverticulitis of small intestine – LB15.4 Congenital diverticulosis of small intestine – LB15.5 Congenital diverticulum of small intestine – LB15.Y Other specified structural developmental anomalies of small intestine – LB15.Z Structural developmental anomalies of small intestine, unspecified LB16 Structural developmental anomalies of large intestine – LB16.0 Congenital absence, atresia or stenosis of large intestine – LB16.1 Hirschsprung disease – LB16.2 Immature ganglionosis of large intestine – LB16.3 Congenital hypoganglionosis of large intestine – LB16.Y Other specified structural developmental anomalies of large intestine – LB16.Z Structural developmental anomalies of large intestine, unspecified LB17 Structural developmental anomalies of anal canal – LB17.0 Anorectal malformations – LB17.1 Ectopic anus – LB17.2 Persistent cloaca – LB17.3 Cloacal exstrophy – LB17.4 Perineal groove – LB17.Y Other specified structural developmental anomalies of anal canal – LB17.Z Structural developmental anomalies of anal canal, unspecified LB18 Congenital anomalies of intestinal fixation LB1Y Other specified structural developmental anomalies of the digestive tract LB1Z Structural developmental anomalies of the digestive tract, unspecified LB20 Structural developmental anomalies of gallbladder, bile ducts or liver – LB20.0 Structural developmental anomalies of liver – LB20.1 Structural developmental anomalies of gallbladder – LB20.2 Structural developmental anomalies of bile ducts – LB20.Y Other specified structural developmental anomalies of gallbladder, bile ducts or liver – LB20.Z Structural developmental anomalies of gallbladder, bile ducts or liver, unspecified –– LB20.00 Fibropolycystic liver disease –– LB20.0Y Other specified structural developmental anomalies of liver –– LB20.0Z Structural developmental anomalies of liver, unspecified –– LB20.10 Agenesis, aplasia or hypoplasia of gallbladder –– LB20.1Y Other specified structural developmental anomalies of gallbladder –– LB20.1Z Structural developmental anomalies of gallbladder, unspecified –– LB20.20 Choledochal cyst –– LB20.21 Biliary atresia –– LB20.22 Congenital stenosis or stricture of bile ducts –– LB20.23 Structural developmental anomalies of cystic duct –– LB20.24 Accessory bile duct –– LB20.2Y Other specified structural developmental anomalies of bile ducts –– LB20.2Z Structural developmental anomalies of bile ducts, unspecified LB21 Structural developmental anomalies of pancreas – LB21.0 Annular pancreas – LB21.1 Pancreas divisum – LB21.2 Accessory pancreas – LB21.3 Agenesis-aplasia of pancreas – LB21.4 Partial agenesis of pancreas – LB21.5 Hypoplasia of pancreas – LB21.Y Other specified structural developmental anomalies of pancreas – LB21.Z Structural developmental anomalies of pancreas, unspecified LB22 Structural developmental anomalies of spleen – LB22.0 Congenital asplenia – LB22.1 Polysplenia – LB22.2 Ectopic spleen – LB22.Y Other specified structural developmental anomalies of spleen – LB22.Z Structural developmental anomalies of spleen, unspecified LB2Y Other specified structural developmental anomalies of the liver, biliary tract, pancreas or spleen LB2Z Structural developmental anomalies of the liver, biliary tract, pancreas or spleen, unspecified LB30 Structural developmental anomalies of kidneys – LB30.0 Renal agenesis or other reduction defects of kidney – LB30.1 Renal dysplasia – LB30.2 Congenital single renal cyst – LB30.3 Renal tubular dysgenesis – LB30.4 Oligomeganephronia – LB30.5 Accessory kidney – LB30.6 Fusion anomaly of kidneys – LB30.7 Ectopic or pelvic kidney – LB30.8 Medullary sponge kidney – LB30.9 Multicystic renal dysplasia – LB30.Y Other specified structural developmental anomalies of kidneys – LB30.Z Structural developmental anomalies of kidneys, unspecified –– LB30.00 Renal agenesis –– LB30.0Y Other specified renal agenesis or other reduction defects of kidney –– LB30.0Z Renal agenesis or other reduction defects of kidney, unspecified –– LB30.60 Lobulated kidney –– LB30.61 Fused pelvic kidney –– LB30.62 Horseshoe kidney –– LB30.6Y Other specified fusion anomaly of kidneys –– LB30.6Z Fusion anomaly of kidneys, unspecified LB31 Structural developmental anomalies of urinary tract – LB31.0 Congenital hydronephrosis – LB31.1 Congenital primary megaureter – LB31.2 Fetal lower urinary tract obstruction – LB31.3 Exstrophy of urinary bladder – LB31.4 Congenital diverticulum of urinary bladder – LB31.5 Duplication of urethra – LB31.6 Congenital megalourethra – LB31.7 Megacystis-megaureter – LB31.8 Atresia or stenosis of ureter – LB31.9 Agenesis of ureter – LB31.A Duplication of ureter – LB31.B Malposition of ureter – LB31.C Congenital absence of bladder or urethra – LB31.D Congenital vesico-uretero-renal reflux – LB31.Y Other specified structural developmental anomalies of urinary tract – LB31.Z Structural developmental anomalies of urinary tract, unspecified LB3Y Other specified structural developmental anomalies of the urinary system LB3Z Structural developmental anomalies of the urinary system, unspecified LB40 Structural developmental anomalies of vulva – LB40.0 Absence of vulva – LB40.1 Embryonic cyst of vulva – LB40.2 Fusion of labia – LB40.Y Other specified structural developmental anomalies of vulva – LB40.Z Structural developmental anomalies of vulva, unspecified LB41 Structural developmental anomalies of clitoris – LB41.0 Agenesis of clitoris – LB41.1 Duplication of clitoris – LB41.2 Clitoromegaly – LB41.Y Other specified structural developmental anomalies of clitoris – LB41.Z Structural developmental anomalies of clitoris, unspecified LB42 Structural developmental anomalies of vagina – LB42.0 Absence of vagina – LB42.1 Septate vagina – LB42.2 Congenital rectovaginal fistula – LB42.3 Tight hymenal ring – LB42.4 Imperforate hymen – LB42.5 Stricture or atresia of vagina – LB42.Y Other specified structural developmental anomalies of vagina – LB42.Z Structural developmental anomalies of vagina, unspecified LB43 Structural developmental anomalies of cervix uteri – LB43.0 Embryonic cyst of cervix – LB43.1 Agenesis or aplasia of cervix – LB43.Y Other specified structural developmental anomalies of cervix uteri – LB43.Z Structural developmental anomalies of cervix uteri, unspecified LB44 Structural developmental anomalies of uterus, except cervix – LB44.0 Agenesis or aplasia of uterine body – LB44.1 Hypoplasia of uterus – LB44.2 Unicornuate uterus – LB44.3 Bicornuate uterus – LB44.4 Septate uterus – LB44.5 Congenital fistulae between uterus and digestive and urinary tracts – LB44.6 Uterovaginal malformation due to diethylstilbestrol syndrome – LB44.Y Other specified structural developmental anomalies of uterus, except cervix – LB44.Z Structural developmental anomalies of uterus, except cervix, unspecified LB45 Structural developmental anomalies of ovaries, fallopian tubes or broad ligaments – LB45.0 Congenital absence of ovary – LB45.1 46,XX gonadal dysgenesis – LB45.2 Developmental ovarian cyst – LB45.3 Congenital torsion of ovary – LB45.4 Accessory ovary – LB45.5 Congenital absence of fallopian tube – LB45.6 Atresia of fallopian tube – LB45.7 Accessory fallopian tube – LB45.8 Embryonic cyst of fallopian tube – LB45.9 Embryonic cyst of broad ligament – LB45.Y Other specified structural developmental anomalies of ovaries, fallopian tubes or broad ligaments – LB45.Z Structural developmental anomalies of ovaries, fallopian tubes or broad ligaments, unspecified LB4Y Other specified structural developmental anomalies of the female genital system LB4Z Structural developmental anomalies of the female genital system, unspecified LB50 Micropenis or penis agenesis LB51 Anorchia or microorchidia LB52 Cryptorchidism – LB52.0 Ectopic testis – LB52.1 Undescended testicle, unilateral – LB52.2 Undescended testicle, bilateral – LB52.Y Other specified cryptorchidism – LB52.Z Cryptorchidism, unspecified LB53 Hypospadias – LB53.0 Hypospadias, balanic – LB53.1 Hypospadias, penile – LB53.2 Hypospadias, penoscrotal – LB53.3 Hypospadias, scrotal – LB53.4 Hypospadias, perineal – LB53.Y Other specified hypospadias – LB53.Z Hypospadias, unspecified –– LB53.00 Hypospadias, coronal –– LB53.01 Hypospadias, glandular –– LB53.0Y Other specified hypospadias, balanic –– LB53.0Z Hypospadias, balanic, unspecified LB54 Congenital chordee LB55 Epispadias LB56 Bifid scrotum LB57 Agenesis of vas deferens LB58 Polyorchidism LB59 Hypoplasia of testis or scrotum LB5Y Other specified structural developmental anomalies of the male genital system LB5Z Structural developmental anomalies of the male genital system, unspecified LB60 Breast aplasia LB61 Absent nipple LB62 Supernumerary breasts LB63 Accessory nipple LB6Y Other specified structural developmental anomalies of the breast LB6Z Structural developmental anomalies of the breast, unspecified LB70 Structural developmental anomalies of cranium – LB70.0 Craniosynostosis – LB70.1 Wormian bones – LB70.2 J-shaped sella turcica – LB70.3 Macrocephaly – LB70.Y Other specified structural developmental anomalies of cranium – LB70.Z Structural developmental anomalies of cranium, unspecified –– LB70.00 Plagiocephaly –– LB70.0Y Other specified craniosynostosis –– LB70.0Z Craniosynostosis, unspecified LB71 Structural developmental anomalies of facial bones – LB71.0 Hypotelorism – LB71.1 Hypertelorism – LB71.Y Other specified structural developmental anomalies of facial bones – LB71.Z Structural developmental anomalies of facial bones, unspecified LB72 Structural developmental anomalies of shoulder girdle – LB72.0 Cervical rib – LB72.1 Sprengel deformity – LB72.2 Deformation of scapula – LB72.Y Other specified structural developmental anomalies of shoulder girdle – LB72.Z Structural developmental anomalies of shoulder girdle, unspecified LB73 Structural developmental anomalies of spine or bony thorax – LB73.0 Occult spinal dysraphism – LB73.1 Structural developmental anomalies of chest wall – LB73.2 Structural developmental anomalies of spine – LB73.Y Other specified structural developmental anomalies of spine or bony thorax – LB73.Z Structural developmental anomalies of spine or bony thorax, unspecified –– LB73.10 Poland syndrome –– LB73.11 Bifid rib –– LB73.12 Accessory rib –– LB73.13 Structural developmental anomalies of sternum –– LB73.1Y Other specified structural developmental anomalies of chest wall –– LB73.1Z Structural developmental anomalies of chest wall, unspecified –– LB73.20 Klippel-Feil anomaly –– LB73.21 Occipitalisation of atlas –– LB73.22 Atlanto-axial instability or subluxation –– LB73.23 Aplasia or hypoplasia of the odontoid process of axis –– LB73.24 Segmentation anomalies of vertebrae –– LB73.25 Congenital scoliosis due to congenital bony malformation –– LB73.26 Sacralisation of the last lumbar vertebra –– LB73.27 Lumbarisation of the first sacral vertebra –– LB73.28 Sacrum agenesis or hypoplasia –– LB73.29 Caudal appendage –– LB73.2A Congenital spondylolisthesis –– LB73.2Y Other specified structural developmental anomalies of spine –– LB73.2Z Structural developmental anomalies of spine, unspecified LB74 Structural developmental anomalies of pelvic girdle – LB74.0 Developmental dysplasia of hip – LB74.1 Congenital subluxation of hip – LB74.2 Unstable hip – LB74.3 Congenital coxa vara – LB74.4 Congenital coxa valga – LB74.5 Wide symphysis pubis – LB74.Y Other specified structural developmental anomalies of pelvic girdle – LB74.Z Structural developmental anomalies of pelvic girdle, unspecified LB75 Brachydactyly – LB75.0 Brachydactyly of fingers – LB75.1 Brachydactyly of toes – LB75.2 Symbrachydactyly of hands or feet – LB75.Y Other specified brachydactyly – LB75.Z Brachydactyly, unspecified LB76 Triphalangeal thumb LB77 Hyperphalangy LB78 Polydactyly – LB78.0 Polydactyly of the thumb – LB78.1 Polysyndactyly – LB78.2 Postaxial polydactyly of fingers – LB78.3 Polydactyly of toes – LB78.Y Other specified polydactyly – LB78.Z Polydactyly, unspecified LB79 Syndactyly – LB79.0 Fused fingers – LB79.1 Webbed fingers – LB79.2 Fused toes – LB79.3 Webbed toes – LB79.Y Other specified syndactyly – LB79.Z Syndactyly, unspecified – LB80 Congenital deformities of fingers –– LB80.0 Clinodactyly of fingers –– LB80.2 Radial deviation of fingers –– LB80.Y Other specified congenital deformities of fingers –– LB80.Z Congenital deformities of fingers, unspecified – LB81 Congenital deformities of toes –– LB81.0 Clinodactyly of toes –– LB81.Y Other specified congenital deformities of toes –– LB81.Z Congenital deformities of toes, unspecified LB90 Joint formation defects – LB90.0 Humero-radio-ulnar synostosis – LB90.1 Humero-radial synostosis – LB90.2 Humero-ulnar synostosis – LB90.3 Radio-ulnar synostosis – LB90.4 Madelung deformity – LB90.5 Congenital digital clubbing – LB90.6 Tibio-fibular synostosis – LB90.7 Cubitus valgus – LB90.8 Cubitus varus – LB90.Y Other specified joint formation defects – LB90.Z Joint formation defects, unspecified LB91 Congenital shoulder dislocation LB92 Congenital elbow dislocation LB93 Congenital knee dislocation – LB93.0 Congenital genu recurvatum – LB93.1 Congenital genu flexum – LB93.Y Other specified congenital knee dislocation – LB93.Z Congenital knee dislocation, unspecified LB94 Congenital patella dislocation LB95 Patella aplasia or hypoplasia LB96 Congenital bowing of long bones – LB96.0 Congenital bowing of femur – LB96.1 Congenital bowing of tibia – LB96.Y Other specified congenital bowing of long bones – LB96.Z Congenital bowing of long bones, unspecified LB97 Limb overgrowth – LB97.0 Macrodactyly of fingers – LB97.1 Macrodactyly of toes – LB97.2 Upper limb hypertrophy – LB97.3 Lower limb hypertrophy – LB97.Y Other specified limb overgrowth – LB97.Z Limb overgrowth, unspecified LB98 Congenital deformities of feet – LB98.0 Congenital varus deformities of feet – LB98.1 Congenital pes planus – LB98.2 Congenital valgus deformities of feet – LB98.3 Congenital pes cavus – LB98.4 Congenital vertical talus – LB98.5 Congenital hammer toe – LB98.Y Other specified congenital deformities of feet – LB98.Z Congenital deformities of feet, unspecified –– LB98.00 Talipes equinovarus –– LB98.01 Talipes calcaneovarus –– LB98.02 Metatarsus varus –– LB98.0Y Other specified congenital varus deformities of feet –– LB98.0Z Congenital varus deformities of feet, unspecified –– LB98.20 Congenital hallux valgus –– LB98.21 Metatarsus valgus –– LB98.22 Talipes calcaneovalgus –– LB98.2Y Other specified congenital valgus deformities of feet –– LB98.2Z Congenital valgus deformities of feet, unspecified LB99 Reduction defects of upper limb – LB99.0 Amelia of upper limb – LB99.1 Humeral agenesis or hypoplasia – LB99.2 Radial hemimelia – LB99.3 Ulnar hemimelia – LB99.4 Congenital absence of upper arm or forearm with hand present – LB99.5 Congenital absence of both forearm and hand – LB99.6 Acheiria – LB99.7 Adactyly of hands – LB99.8 Split hand – LB99.Y Other specified reduction defects of upper limb – LB99.Z Reduction defects of upper limb, unspecified LB9A Reduction defects of lower limb – LB9A.0 Amelia of lower limb – LB9A.1 Tibial hemimelia – LB9A.2 Fibular hemimelia – LB9A.3 Congenital absence of thigh or lower leg with foot present – LB9A.4 Apodia – LB9A.5 Adactyly of feet – LB9A.6 Split foot – LB9A.7 Congenital absence of both lower leg and foot – LB9A.8 Femoral agenesis or hypoplasia – LB9A.Y Other specified reduction defects of lower limb – LB9A.Z Reduction defects of lower limb, unspecified LB9B Reduction defects of upper and lower limbs LB9Y Other specified structural developmental anomalies of the skeleton LB9Z Structural developmental anomalies of the skeleton, unspecified – LC00 Keratinocytic epidermal hamartoma –– LC00.0 Epidermal naevus –– LC00.Y Other specified keratinocytic epidermal hamartoma –– LC00.Z Keratinocytic epidermal hamartoma, unspecified – LC01 Pilosebaceous hamartoma – LC02 Complex epidermal hamartoma – LC0Y Other specified developmental hamartomata of the epidermis and epidermal appendages – LC10 Dermal melanocytosis – LC1Y Other specified developmental anomalies of skin pigmentation – LC20 Connective tissue hamartoma – LC2Y Other specified hamartomata derived from dermal connective tissue – LC30 Developmental defects of hair or hair growth – LC31 Developmental defects of the nail apparatus LC40 Dermoid cyst – LC50 Developmental capillary vascular malformations of the skin –– LC50.0 Salmon patch –– LC50.1 Port-wine stain –– LC50.Y Other specified cutaneous capillary vascular malformation – LC51 Developmental venous malformations involving the skin – LC52 Complex or combined developmental vascular malformations involving the skin – LC5Y Other specified developmental anomalies of cutaneous vasculature – LC5Z Developmental anomalies of cutaneous vasculature, unspecified – LC60 Aplasia cutis congenita LC7Y Other specified structural developmental anomalies of the skin LC7Z Structural developmental anomalies of the skin, unspecified LC80 Congenital adrenal hypoplasia LC8Y Other specified structural developmental anomalies of the adrenal glands LC8Z Structural developmental anomalies of the adrenal glands, unspecified LD0Y Other specified structural developmental anomalies primarily affecting one body system LD0Z Structural developmental anomalies primarily affecting one body system, unspecified LD20 Syndromes with central nervous system anomalies as a major feature LD20.0 Syndromes with cerebellar anomalies as a major feature LD20.1 Syndromes with lissencephaly as a major feature LD20.2 Syndromes with microcephaly as a major feature LD20.3 Syndromes with holoprosencephaly as a major feature LD20.4 Syndromes with brain calcifications as a major feature LD20.Y Other specified syndromes with central nervous system anomalies as a major feature LD20.Z Syndromes with central nervous system anomalies as a major feature, unspecified – LD20.00 Joubert syndrome – LD20.01 Pontocerebellar hypoplasia – LD20.0Y Other specified syndromes with cerebellar anomalies as a major feature – LD20.0Z Syndromes with cerebellar anomalies as a major feature, unspecified LD21 Syndromes with eye anomalies as a major feature LD21.0 Syndromes with microphthalmia as a major feature LD21.Y Other specified syndromes with eye anomalies as a major feature LD21.Z Syndromes with eye anomalies as a major feature, unspecified LD22 Syndromes with dental anomalies as a major feature LD23 Syndromes with vascular anomalies as a major feature LD24 Syndromes with skeletal anomalies as a major feature LD24.0 Syndromes with micromelia LD24.1 Bone diseases with increased bone density LD24.2 Bone diseases with disorganised development of skeletal components LD24.3 Spondyloepiphyseal or spondyloepimetaphyseal dysplasias LD24.4 Spondylometaphyseal dysplasias LD24.5 Spondylodysplastic dysplasias LD24.6 Multiple epiphyseal dysplasia or pseudoachondroplasia LD24.7 Multiple metaphyseal dysplasias LD24.8 Acromelic dysplasias LD24.9 Acromesomelic dysplasias LD24.A Mesomelic or rhizomesomelic dysplasias LD24.B Short rib syndromes LD24.C Bent bone dysplasias LD24.D Slender bone dysplasias LD24.E Bone dysplasias with multiple joint dislocations LD24.F Progressive ossification of skin, skeletal muscle, fascia, tendons or ligaments LD24.G Syndromic craniosynostoses LD24.H Dysostoses with predominant vertebral and costal involvement LD24.J Patellar dysostoses LD24.K Genetic bone diseases with decreased bone density LD24.Y Other specified syndromes with skeletal anomalies as a major feature LD24.Z Syndromes with skeletal anomalies as a major feature, unspecified – LD24.00 Achondroplasia – LD24.01 Hypochondroplasia – LD24.02 Thanatophoric dysplasia – LD24.03 Diastrophic dysplasia – LD24.04 Chondrodysplasia punctata – LD24.0Y Other specified syndromes with micromelia – LD24.0Z Syndromes with micromelia, unspecified – LD24.10 Osteopetrosis – LD24.11 Osteopoikilosis – LD24.1Y Other specified bone diseases with increased bone density – LD24.1Z Bone diseases with increased bone density, unspecified – LD24.20 Multiple osteochondromas – LD24.21 Exostoses with anetodermia and brachydactyly type E – LD24.22 Cherubism – LD24.23 Yunis-Varon disease – LD24.2Y Other specified bone diseases with disorganised development of skeletal components – LD24.2Z Bone diseases with disorganised development of skeletal components, unspecified – LD24.50 Achondrogenesis – LD24.51 Hypochondrogenesis – LD24.5Y Other specified spondylodysplastic dysplasias – LD24.5Z Spondylodysplastic dysplasias, unspecified – LD24.60 Pseudoachondroplasia – LD24.61 Multiple epiphyseal dysplasias – LD24.6Y Other specified multiple epiphyseal dysplasia or pseudoachondroplasia – LD24.6Z Multiple epiphyseal dysplasia or pseudoachondroplasia, unspecified – LD24.80 Langer-Giedion syndrome – LD24.8Y Other specified acromelic dysplasias – LD24.8Z Acromelic dysplasias, unspecified – LD24.B0 Short rib-polydactyly syndrome – LD24.B1 Asphyxiating thoracic dystrophy – LD24.BY Other specified short rib syndromes – LD24.BZ Short rib syndromes, unspecified – LD24.G0 Pfeiffer syndrome – LD24.G1 Crouzon disease – LD24.G2 Apert syndrome – LD24.GY Other specified syndromic craniosynostoses – LD24.GZ Syndromic craniosynostoses, unspecified – LD24.J0 Nail-patella syndrome – LD24.JY Other specified patellar dysostoses – LD24.JZ Patellar dysostoses, unspecified – LD24.K0 Osteogenesis imperfecta – LD24.KY Other specified genetic bone diseases with decreased bone density – LD24.KZ Genetic bone diseases with decreased bone density, unspecified LD25 Syndromes with face or limb anomalies as a major feature LD25.0 Oromandibular-limb anomaly syndrome LD25.1 Fronto-otopalatodigital syndromes LD25.2 Acrofacial dysostoses LD25.3 Craniofacial dysostoses LD25.Y Other specified syndromes with face or limb anomalies as a major feature LD25.Z Syndromes with face or limb anomalies as a major feature, unspecified – LD25.00 Oral-facial-digital syndrome – LD25.0Y Other specified oromandibular-limb anomaly syndrome – LD25.0Z Oromandibular-limb anomaly syndrome, unspecified LD26 Syndromes with limb anomalies as a major feature LD26.0 Combined reduction defects of upper and lower limbs LD26.1 Complex brachydactylies LD26.2 Syndromes with limb duplication, polydactyly, syndactyly or triphalangism LD26.3 Syndromes with synostoses of limbs LD26.4 Arthrogryposis syndromes LD26.5 Constriction rings LD26.6 Congenital vascular bone syndromes LD26.Y Other specified syndromes with limb anomalies as a major feature LD26.Z Syndromes with limb anomalies as a major feature, unspecified – LD26.40 Multiple pterygium syndrome – LD26.41 Arthrogryposis multiplex congenita – LD26.4Y Other specified arthrogryposis syndromes – LD26.4Z Arthrogryposis syndromes, unspecified – LD26.60 Angio-osteohypertrophic syndrome – LD26.6Y Other specified congenital vascular bone syndromes – LD26.6Z Congenital vascular bone syndromes, unspecified LD27 Syndromes with skin or mucosal anomalies as a major feature LD27.0 Ectodermal dysplasia syndromes LD27.1 Xeroderma pigmentosum LD27.2 Syndromic ichthyosis LD27.3 Genetic syndromes with hypertrichosis LD27.4 Genetic syndromes affecting nails LD27.5 Genetic hamartoneoplastic syndromes affecting the skin LD27.6 Genetic lipodystrophy LD27.Y Other specified syndromes with skin or mucosal anomalies as a major feature LD27.Z Syndromes with skin or mucosal anomalies as a major feature, unspecified – LD27.00 Incontinentia pigmenti – LD27.01 Cronkhite-Canada syndrome – LD27.02 Hypohidrotic ectodermal dysplasia – LD27.03 Hidrotic ectodermal dysplasia, Clouston type – LD27.0Y Other specified ectodermal dysplasia syndromes – LD27.60 Congenital generalised lipodystrophy – LD27.6Z Genetic lipodystrophy, unspecified LD28 Syndromes with connective tissue involvement as a major feature LD28.0 Marfan syndrome or Marfan-related disorders LD28.1 Ehlers-Danlos syndrome LD28.2 Genetically-determined cutis laxa LD28.Y Other specified syndromes with connective tissue involvement as a major feature LD28.Z Syndromes with connective tissue involvement as a major feature, unspecified – LD28.00 Congenital contractural arachnodactyly – LD28.01 Marfan syndrome – LD28.0Y Other specified Marfan syndrome or Marfan-related disorders – LD28.0Z Marfan syndrome or Marfan-related disorders, unspecified – LD28.10 Ehlers-Danlos syndrome, classical type – LD28.1Y Other specified types of Ehlers-Danlos syndrome LD29 Syndromes with obesity as a major feature LD2A Malformative disorders of sex development LD2A.0 Ovotesticular disorder of sex development LD2A.1 46,XY gonadal dysgenesis LD2A.2 Testicular agenesis LD2A.3 46,XY disorder of sex development due to a defect in testosterone metabolism LD2A.4 46,XY disorder of sex development due to androgen resistance LD2A.Y Other specified malformative disorders of sex development LD2A.Z Malformative disorders of sex development, unspecified LD2B Syndromes with premature ageing appearance as a major feature LD2C Overgrowth syndromes LD2D Phakomatoses or hamartoneoplastic syndromes LD2D.0 Peutz-Jeghers syndrome LD2D.1 Neurofibromatoses LD2D.2 Tuberous sclerosis LD2D.3 Gardner syndrome LD2D.4 Gorlin syndrome LD2D.Y Other specified phakomatoses or hamartoneoplastic syndromes LD2D.Z Phakomatoses or hamartoneoplastic syndromes, unspecified – LD2D.10 Neurofibromatosis type 1 – LD2D.11 Neurofibromatosis type 2 – LD2D.12 Neurofibromatosis type 3 – LD2D.1Y Other specified neurofibromatoses – LD2D.1Z Neurofibromatosis, unspecified LD2E Syndromes with structural anomalies due to inborn errors of metabolism LD2F Syndromes with multiple structural anomalies, without predominant body system involvement LD2F.0 Toxic or drug-related embryofetopathies LD2F.1 Syndromes with multiple structural anomalies, not of environmental origin LD2F.Y Other specified syndromes with multiple structural anomalies, without predominant body system involvement LD2F.Z Syndromes with multiple structural anomalies, without predominant body system involvement, unspecified – LD2F.00 Fetal alcohol syndrome – LD2F.01 Fetal hydantoin syndrome – LD2F.02 Embryofetopathy due to oral anticoagulant therapy – LD2F.03 Fetal Valproate Spectrum Disorder – LD2F.0Y Other specified toxic or drug-related embryofetopathies – LD2F.0Z Toxic or drug-related embryofetopathies, unspecified – LD2F.10 Prune belly syndrome – LD2F.11 VATER association – LD2F.12 Sirenomelia – LD2F.13 Meckel-Gruber syndrome – LD2F.14 MURCS association – LD2F.15 Noonan syndrome – LD2F.16 Otomandibular dysplasia – LD2F.1Y Other specified syndromes with multiple structural anomalies, not of environmental origin – LD2F.1Z Syndromes with multiple structural anomalies, not of environmental origin, unspecified LD2G Conjoined twins LD2H Syndromic genetic deafness LD2H.0 Fraser syndrome LD2H.1 Neuropathy with hearing impairment LD2H.2 Progressive deafness with stapes fixation LD2H.3 Waardenburg-Shah syndrome LD2H.4 Usher syndrome LD2H.Y Other specified syndromic genetic deafness LD2H.Z Syndromic genetic deafness, unspecified LD2Y Other specified multiple developmental anomalies or syndromes LD2Z Multiple developmental anomalies or syndromes, unspecified LD40 Complete trisomies of the autosomes LD40.0 Complete trisomy 21 LD40.1 Complete trisomy 13 LD40.2 Complete trisomy 18 LD40.Y Other specified complete trisomies of the autosomes LD40.Z Complete trisomies of the autosomes, unspecified LD41 Duplications of the autosomes LD41.0 Duplications of chromosome 1 LD41.1 Duplications of chromosome 2 LD41.2 Duplications of chromosome 3 LD41.3 Duplications of chromosome 4 LD41.4 Duplications of chromosome 5 LD41.5 Duplications of chromosome 6 LD41.6 Duplications of chromosome 7 LD41.7 Duplications of chromosome 8 LD41.8 Duplications of chromosome 9 LD41.9 Duplications of chromosome 10 LD41.A Duplications of chromosome 11 LD41.B Duplications of chromosome 12 LD41.C Duplications of chromosome 13 LD41.D Duplications of chromosome 14 LD41.E Duplications of chromosome 15 LD41.F Duplications of chromosome 16 LD41.G Duplications of chromosome 17 LD41.H Duplications of chromosome 18 LD41.J Duplications of chromosome 19 LD41.K Duplications of chromosome 20 LD41.L Duplications of chromosome 21 LD41.M Duplications of chromosome 22 LD41.N Extra ring or dicentric chromosomes LD41.P Duplications with other complex rearrangements LD41.Q Extra marker chromosomes LD41.Y Other specified duplications of the autosomes LD41.Z Duplications of the autosomes, unspecified – LD41.00 Duplications of the long arm of chromosome 1 – LD41.01 Duplications of the short arm of chromosome 1 – LD41.0Y Other specified duplications of chromosome 1 – LD41.0Z Duplications of chromosome 1, unspecified – LD41.10 Duplications of the long arm of chromosome 2 – LD41.11 Duplications of the short arm of chromosome 2 – LD41.1Y Other specified duplications of chromosome 2 – LD41.1Z Duplications of chromosome 2, unspecified – LD41.20 Duplications of the long arm of chromosome 3 – LD41.21 Duplications of the short arm of chromosome 3 – LD41.2Y Other specified duplications of chromosome 3 – LD41.2Z Duplications of chromosome 3, unspecified – LD41.30 Duplications of the long arm of chromosome 4 – LD41.31 Duplications of the short arm of chromosome 4 – LD41.3Y Other specified duplications of chromosome 4 – LD41.3Z Duplications of chromosome 4, unspecified – LD41.40 Duplications of the long arm of chromosome 5 – LD41.41 Duplications of the short arm of chromosome 5 – LD41.4Y Other specified duplications of chromosome 5 – LD41.4Z Duplications of chromosome 5, unspecified – LD41.50 Duplications of the long arm of chromosome 6 – LD41.51 Duplications of the short arm of chromosome 6 – LD41.5Y Other specified duplications of chromosome 6 – LD41.5Z Duplications of chromosome 6, unspecified – LD41.60 Duplications of the long arm of chromosome 7 – LD41.61 Duplications of the short arm of chromosome 7 – LD41.6Y Other specified duplications of chromosome 7 – LD41.6Z Duplications of chromosome 7, unspecified – LD41.70 Duplications of the long arm of chromosome 8 – LD41.71 Duplications of the short arm of chromosome 8 – LD41.7Y Other specified duplications of chromosome 8 – LD41.7Z Duplications of chromosome 8, unspecified – LD41.80 Duplications of the long arm of chromosome 9 – LD41.81 Duplications of the short arm of chromosome 9 – LD41.8Y Other specified duplications of chromosome 9 – LD41.8Z Duplications of chromosome 9, unspecified – LD41.90 Duplications of the long arm of chromosome 10 – LD41.91 Duplications of the short arm of chromosome 10 – LD41.9Y Other specified duplications of chromosome 10 – LD41.9Z Duplications of chromosome 10, unspecified – LD41.B0 Duplications of the long arm of chromosome 12 – LD41.B1 Duplications of the short arm of chromosome 12 – LD41.BY Other specified duplications of chromosome 12 – LD41.BZ Duplications of chromosome 12, unspecified – LD41.F0 Duplications of the long arm of chromosome 16 – LD41.F1 Duplications of the short arm of chromosome 16 – LD41.FY Other specified duplications of chromosome 16 – LD41.FZ Duplications of chromosome 16, unspecified – LD41.G0 Duplications of the long arm of chromosome 17 – LD41.G1 Duplications of the short arm of chromosome 17 – LD41.GY Other specified duplications of chromosome 17 – LD41.GZ Duplications of chromosome 17, unspecified – LD41.H0 Duplications of the long arm of chromosome 18 – LD41.H1 Duplications of the short arm of chromosome 18 – LD41.HY Other specified duplications of chromosome 18 – LD41.HZ Duplications of chromosome 18, unspecified – LD41.J0 Duplications of the long arm of chromosome 19 – LD41.J1 Duplications of the short arm of chromosome 19 – LD41.JY Other specified duplications of chromosome 19 – LD41.JZ Duplications of chromosome 19, unspecified – LD41.K0 Duplications of the long arm of chromosome 20 – LD41.K1 Duplications of the short arm of chromosome 20 – LD41.KY Other specified duplications of chromosome 20 – LD41.KZ Duplications of chromosome 20, unspecified LD42 Polyploidies LD42.0 Triploidy LD42.1 Tetraploidy LD42.Y Other specified polyploidies LD42.Z Polyploidies, unspecified LD43 Complete monosomies of the autosomes LD43.0 Complete monosomy of autosome LD43.1 Mosaic monosomy of autosome LD43.Y Other specified complete monosomies of the autosomes LD43.Z Complete monosomies of the autosomes, unspecified LD44 Deletions of the autosomes LD44.1 Deletions of chromosome 1 LD44.2 Deletions of chromosome 2 LD44.3 Deletions of chromosome 3 LD44.4 Deletions of chromosome 4 LD44.5 Deletions of chromosome 5 LD44.6 Deletions of chromosome 6 LD44.7 Deletions of chromosome 7 LD44.8 Deletions of chromosome 8 LD44.9 Deletions of chromosome 9 LD44.A Deletions of chromosome 10 LD44.B Deletions of chromosome 11 LD44.C Deletions of chromosome 12 LD44.D Deletions of chromosome 13 LD44.E Deletions of chromosome 14 LD44.F Deletions of chromosome 15 LD44.G Deletions of chromosome 16 LD44.H Deletions of chromosome 17 LD44.J Deletions of chromosome 18 LD44.K Deletions of chromosome 19 LD44.L Deletions of chromosome 20 LD44.M Deletions of chromosome 21 LD44.N Deletions of chromosome 22 LD44.P Deletions with other complex rearrangements LD44.Y Other specified deletions of the autosomes LD44.Z Deletions of the autosomes, unspecified – LD44.10 Deletions of the long arm of chromosome 1 – LD44.11 Deletions of the short arm of chromosome 1 – LD44.1Y Other specified deletions of chromosome 1 – LD44.1Z Deletions of chromosome 1, unspecified – LD44.20 Deletions of the long arm of chromosome 2 – LD44.21 Deletions of the short arm of chromosome 2 – LD44.2Y Other specified deletions of chromosome 2 – LD44.2Z Deletions of chromosome 2, unspecified – LD44.30 Deletions of the long arm of chromosome 3 – LD44.31 Deletions of the short arm of chromosome 3 – LD44.3Y Other specified deletions of chromosome 3 – LD44.3Z Deletions of chromosome 3, unspecified – LD44.40 Deletions of the long arm of chromosome 4 – LD44.41 Deletions of the short arm of chromosome 4 – LD44.4Y Other specified deletions of chromosome 4 – LD44.4Z Deletions of chromosome 4, unspecified – LD44.50 Deletions of the long arm of chromosome 5 – LD44.51 Deletions of the short arm of chromosome 5 – LD44.5Y Other specified deletions of chromosome 5 – LD44.5Z Deletions of chromosome 5, unspecified – LD44.60 Deletions of the long arm of chromosome 6 – LD44.61 Deletions of the short arm of chromosome 6 – LD44.6Y Other specified deletions of chromosome 6 – LD44.6Z Deletions of chromosome 6, unspecified – LD44.70 Deletions of the long arm of chromosome 7 – LD44.71 Deletions of the short arm of chromosome 7 – LD44.7Y Other specified deletions of chromosome 7 – LD44.7Z Deletions of chromosome 7, unspecified – LD44.80 Deletions of the long arm of chromosome 8 – LD44.81 Deletions of the short arm of chromosome 8 – LD44.8Y Other specified deletions of chromosome 8 – LD44.8Z Deletions of chromosome 8, unspecified – LD44.90 Deletions of the long arm of chromosome 9 – LD44.91 Deletions of the short arm of chromosome 9 – LD44.9Y Other specified deletions of chromosome 9 – LD44.9Z Deletions of chromosome 9, unspecified – LD44.A0 Deletions of the long arm of chromosome 10 – LD44.A1 Deletions of the short arm of chromosome 10 – LD44.AY Other specified deletions of chromosome 10 – LD44.AZ Deletions of chromosome 10, unspecified – LD44.B0 Deletions of the long arm of chromosome 11 – LD44.B1 Deletions of the short arm of chromosome 11 – LD44.BY Other specified deletions of chromosome 11 – LD44.BZ Deletions of chromosome 11, unspecified – LD44.C0 Deletions of the long arm of chromosome 12 – LD44.C1 Deletions of the short arm of chromosome 12 – LD44.CY Other specified deletions of chromosome 12 – LD44.CZ Deletions of chromosome 12, unspecified – LD44.G0 Deletions of the long arm of chromosome 16 – LD44.G1 Deletions of the short arm of chromosome 16 – LD44.GY Other specified deletions of chromosome 16 – LD44.GZ Deletions of chromosome 16, unspecified – LD44.H0 Deletions of the long arm of chromosome 17 – LD44.H1 Deletions of the short arm of chromosome 17 – LD44.HY Other specified deletions of chromosome 17 – LD44.HZ Deletions of chromosome 17, unspecified – LD44.J0 Deletions of the long arm of chromosome 18 – LD44.J1 Deletions of the short arm of chromosome 18 – LD44.JY Other specified deletions of chromosome 18 – LD44.JZ Deletions of chromosome 18, unspecified – LD44.K0 Deletions of the long arm of chromosome 19 – LD44.K1 Deletions of the short arm of chromosome 19 – LD44.KY Other specified deletions of chromosome 19 – LD44.KZ Deletions of chromosome 19, unspecified – LD44.L0 Deletions of the long arm of chromosome 20 – LD44.L1 Deletions of the short arm of chromosome 20 – LD44.LY Other specified deletions of chromosome 20 – LD44.LZ Deletions of chromosome 20, unspecified – LD44.N0 CATCH 22 phenotype – LD44.NY Other specified deletions of chromosome 22 – LD44.NZ Deletions of chromosome 22, unspecified LD45 Uniparental disomies LD45.0 Uniparental disomies of maternal origin LD45.1 Uniparental disomies of paternal origin LD45.Y Other specified uniparental disomies LD45.Z Uniparental disomies, unspecified LD46 Imprinting errors LD46.0 Maternal imprinting error LD46.1 Paternal imprinting error LD46.Y Other specified imprinting errors LD46.Z Imprinting errors, unspecified LD47 Balanced rearrangements or structural rearrangements LD47.0 Balanced translocation and insertion in normal individual LD47.1 Chromosome inversion in normal individual LD47.2 Balanced autosomal rearrangement in abnormal individual LD47.3 Balanced sex or autosomal rearrangement in abnormal individual LD47.4 Autosomal fragile site LD47.Y Other specified balanced rearrangements or structural rearrangements LD47.Z Balanced rearrangements or structural rearrangements, unspecified LD50 Number anomalies of chromosome X – LD50.0 Turner syndrome – LD50.1 Karyotype 47,XXX – LD50.2 Mosaicism, lines with various numbers of X chromosomes – LD50.3 Klinefelter syndrome – LD50.Y Other specified number anomalies of chromosome X – LD50.Z Number anomalies of chromosome X, unspecified –– LD50.00 Karyotype 45, X –– LD50.01 Karyotype 46, X iso Xq –– LD50.02 Karyotype 46, X with abnormal sex chromosome, except iso Xq –– LD50.03 Mosaicism, 45, X, 46, XX or XY –– LD50.04 Mosaicism, 45, X or other cell line with abnormal sex chromosome –– LD50.30 Klinefelter syndrome with karyotype 47,XXY, regular –– LD50.31 Klinefelter syndrome, male with more than two X chromosomes –– LD50.3Y Other specified Klinefelter syndrome –– LD50.3Z Klinefelter syndrome, unspecified LD51 Structural anomalies of chromosome X, excluding Turner syndrome LD52 Number anomalies of chromosome Y – LD52.0 Male with 46,XX karyotype – LD52.1 Male with double or multiple Y – LD52.Y Other specified number anomalies of chromosome Y – LD52.Z Number anomalies of chromosome Y, unspecified LD53 Structural anomalies of chromosome Y LD54 Male with sex chromosome mosaicism LD55 Fragile X chromosome LD56 Chimaera 46, XX, 46, XY – LD56.0 Androgenetic chimaera – LD56.1 Gynogenetic chimaera – LD56.Y Other specified chimaera 46, XX, 46, XY – LD56.Z Chimaera 46, XX, 46, XY, unspecified LD5Y Other specified sex chromosome anomalies LD5Z Sex chromosome anomalies, unspecified LD7Y Other specified chromosomal anomalies, excluding gene mutations LD7Z Chromosomal anomalies, excluding gene mutations, unspecified LD90 Conditions with disorders of intellectual development as a relevant clinical feature LD90.0 Angelman syndrome LD90.1 Early-onset parkinsonism - intellectual deficit LD90.2 Pelizaeus-Merzbacher-like disease LD90.3 Prader-Willi syndrome LD90.4 Rett syndrome LD90.Y Other specified conditions with disorders of intellectual development as a relevant clinical feature LD90.Z Conditions with disorders of intellectual development as a relevant clinical feature, unspecified LD9Y Other specified developmental anomalies LD9Z Developmental anomalies, unspecified
synonyms Secondary amenorrhoea secondary physiologic amenorrhoea Premature ovarian failure due to autoimmune oophoritis
Thank you for choosing Find-A-Code, please Sign In to remove ads.
Quick, Current, Complete - www.findacode.com