Excludes1 Notes in Chapter 4: Endocrine, nutritional and metabolic diseases ICD-10-CM
An Excludes1 note means "NOT CODED HERE": the excluded code should never be reported together with the code above the note. In Chapter 4 (E00-E89), notes printed in the chapter name other codes 295 times, and Excludes1 Notes anywhere in the Tabular List name the chapter’s codes 322 times, covering 177 distinct codes, categories and ranges. Switch views to read the list either way.
Excludes1 Notes by the code that carries the note
- subclinical iodine-deficiency hypothyroidism (E02)
- E03.0 Congenital hypothyroidism with diffuse goiter
- transitory congenital goiter with normal function (P72.0)
- E03.4 Atrophy of thyroid (acquired)
- congenital atrophy of thyroid (E03.1)
- postpartum thyroiditis (O90.5)
- E06.1 Subacute thyroiditis
- autoimmune thyroiditis (E06.3)
- E06.2 Chronic thyroiditis with transient thyrotoxicosis
- autoimmune thyroiditis (E06.3)
- E07.1 Dyshormogenetic goiter
- transitory congenital goiter with normal function (P72.0)
- drug or chemical induced diabetes mellitus (E09.-)
- gestational diabetes (O24.4-)
- neonatal diabetes mellitus (P70.2)
- postpancreatectomy diabetes mellitus (E13.-)
- postprocedural diabetes mellitus (E13.-)
- secondary diabetes mellitus NEC (E13.-)
- type 1 diabetes mellitus (E10.-)
- type 2 diabetes mellitus (E11.-)
- diabetes mellitus due to underlying condition (E08.-)
- gestational diabetes (O24.4-)
- neonatal diabetes mellitus (P70.2)
- postpancreatectomy diabetes mellitus (E13.-)
- postprocedural diabetes mellitus (E13.-)
- secondary diabetes mellitus NEC (E13.-)
- type 1 diabetes mellitus (E10.-)
- type 2 diabetes mellitus (E11.-)
- diabetes mellitus due to underlying condition (E08.-)
- drug or chemical induced diabetes mellitus (E09.-)
- gestational diabetes (O24.4-)
- hyperglycemia NOS (R73.9)
- neonatal diabetes mellitus (P70.2)
- postpancreatectomy diabetes mellitus (E13.-)
- postprocedural diabetes mellitus (E13.-)
- secondary diabetes mellitus NEC (E13.-)
- type 2 diabetes mellitus (E11.-)
- diabetes mellitus due to underlying condition (E08.-)
- drug or chemical induced diabetes mellitus (E09.-)
- gestational diabetes (O24.4-)
- neonatal diabetes mellitus (P70.2)
- postpancreatectomy diabetes mellitus (E13.-)
- postprocedural diabetes mellitus (E13.-)
- secondary diabetes mellitus NEC (E13.-)
- type 1 diabetes mellitus (E10.-)
- E11.9 Type 2 diabetes mellitus without complications
- type 2 diabetes mellitus, without complications in remission (E11.A)
- E11.A Type 2 diabetes mellitus without complications in remission
- diabetes (mellitus) due to autoimmune process (E10.-)
- diabetes (mellitus) due to immune mediated pancreatic islet beta-cell destruction (E10.-)
- diabetes mellitus due to underlying condition (E08.-)
- drug or chemical induced diabetes mellitus (E09.-)
- gestational diabetes (O24.4-)
- neonatal diabetes mellitus (P70.2)
- type 1 diabetes mellitus (E10.-)
- E16.0 Drug-induced hypoglycemia without coma
- diabetes with hypoglycemia without coma (E09.649)
- E16.1 Other hypoglycemia
- E16.2 Hypoglycemia, unspecified
- E21.1 Secondary hyperparathyroidism, not elsewhere classified
- secondary hyperparathyroidism of renal origin (N25.81)
- E22.0 Acromegaly and pituitary gigantism
- E23.2 Diabetes insipidus
- nephrogenic diabetes insipidus (N25.1)
- E23.3 Hypothalamic dysfunction, not elsewhere classified
- congenital adrenal hyperplasia (E25.0)
- E27.0 Other adrenocortical overactivity
- Cushing's syndrome (E24.-)
- E27.1 Primary adrenocortical insufficiency
- E28.8 Other ovarian dysfunction
- postprocedural ovarian failure (E89.4-)
- E29.1 Testicular hypofunction
- postprocedural testicular hypofunction (E89.5)
- E30.1 Precocious puberty
- E31.1 Polyglandular hyperfunction
- E32.8 Other diseases of thymus
- pseudohypoparathyroidism (E20.1)
- E34.2 Ectopic hormone secretion, not elsewhere classified
- ectopic ACTH syndrome (E24.3)
- achondroplastic short stature (Q77.4)
- hypochondroplastic short stature (Q77.4)
- nutritional short stature (E45)
- pituitary short stature (E23.0)
- progeria (E34.8)
- renal short stature (N25.0)
- Russell-Silver syndrome (Q87.19)
- short-limbed stature with immunodeficiency (D82.2)
- short stature (child) (R62.52)
- short stature NOS (R62.52)
- E35 Disorders of endocrine glands in diseases classified elsewhere
- Echinococcus granulosus infection of thyroid gland (B67.3)
- meningococcal hemorrhagic adrenalitis (A39.1)
- syphilis of endocrine gland (A52.79)
- tuberculosis of adrenal gland, except calcification (A18.7)
- tuberculosis of endocrine gland NEC (A18.82)
- tuberculosis of thyroid gland (A18.81)
- Waterhouse-Friderichsen syndrome (A39.1)
- E36.0 Intraoperative hemorrhage and hematoma of an endocrine system organ or structure complicating a procedure applies to 2 codes
- intraoperative hemorrhage and hematoma of an endocrine system organ or structure due to accidental puncture or laceration during a procedure (E36.1-)
- E40 Kwashiorkor
- marasmic kwashiorkor (E42)
- E41 Nutritional marasmus
- marasmic kwashiorkor (E42)
- E46 Unspecified protein-calorie malnutrition
- nutritional deficiency NOS (E63.9)
- sequelae of vitamin A deficiency (E64.1)
- sequelae of thiamine deficiency (E64.8)
- E52 Niacin deficiency [pellagra]
- sequelae of niacin deficiency (E64.8)
- sequelae of vitamin B deficiency (E64.8)
- E53.1 Pyridoxine deficiency
- pyridoxine-responsive sideroblastic anemia (D64.3)
- E53.8 Deficiency of other specified B group vitamins
- folate deficiency anemia (D52.-)
- E54 Ascorbic acid deficiency
- E55.0 Rickets, active
- sequelae of other vitamin deficiencies (E64.8)
- E56.1 Deficiency of vitamin K
- E58 Dietary calcium deficiency
- E59 Dietary selenium deficiency
- sequelae of selenium deficiency (E64.8)
- E61.1 Iron deficiency
- iron deficiency anemia (D50.-)
- E66.01 Morbid (severe) obesity due to excess calories
- morbid (severe) obesity with alveolar hypoventilation (E66.2)
- transitory tyrosinemia of newborn (P74.5)
- E71.313 Glutaric aciduria type II
- glutaric aciduria (type 1) NOS (E72.3)
- Muscle carnitine palmitoyltransferase deficiency (E71.314)
- Schilder's disease (G37.0)
- Refsum's disease (G60.1)
- E71.511 Neonatal adrenoleukodystrophy
- X-linked adrenoleukodystrophy (E71.42-)
- disorders of tryptophan metabolism (E70.5)
- E72.04 Cystinosis
- Fanconi (-de Toni) (-Debré) syndrome without cystinosis (E72.09)
- disorders of ornithine metabolism (E72.4)
- E72.20 Disorder of urea cycle metabolism, unspecified
- E72.3 Disorders of lysine and hydroxylysine metabolism
- E72.4 Disorders of ornithine metabolism
- hereditary choroidal dystrophy (H31.2-)
- secondary hyperoxaluria (E72.54-)
- primary hyperoxaluria (E72.53-)
- muscle phosphofructokinase deficiency (E74.09)
- E74.4 Disorders of pyruvate metabolism and gluconeogenesis
- adrenoleukodystrophy [Addison-Schilder] (E71.528)
- E78.2 Mixed hyperlipidemia
- Niemann-Pick disease type C (E75.242)
- E83.31 Familial hypophosphatemia
- vitamin D-deficiency rickets (E55.0)
- E84.11 Meconium ileus in cystic fibrosis
- meconium ileus not due to cystic fibrosis (P76.0)
- E87.1 Hypo-osmolality and hyponatremia
- syndrome of inappropriate secretion of antidiuretic hormone (E22.2)
- histiocytosis X (chronic) (C96.6)
- Whipple's disease (K90.81)
- E88.89 Other specified metabolic disorders
- adult pulmonary Langerhans cell histiocytosis (J84.82)
- E88.A Wasting disease (syndrome) due to underlying condition
- E89.1 Postprocedural hypoinsulinemia
- E01 Iodine-deficiency related thyroid disorders and allied conditions: congenital iodine-deficiency syndrome (E00.-)
- E02 Subclinical iodine-deficiency hypothyroidism
- E03.0 Congenital hypothyroidism with diffuse goiter
- E03.0-E03.1 Congenital hypothyroidism with diffuse goiter to Congenital hypothyroidism without goiter 2 codes
- P72 Other transitory neonatal endocrine disorders: congenital hypothyroidism with or without goiter (E03.0-E03.1)
- E03.1 Congenital hypothyroidism without goiter
- E03.9 Hypothyroidism, unspecified
- L98.5 Mucinosis of the skin: myxedema (E03.9)
- E22 Hyperfunction of pituitary gland: overproduction of thyroid-stimulating hormone (E05.8-)
- E06.2 Chronic thyroiditis with transient thyrotoxicosis
- E05 Thyrotoxicosis [hyperthyroidism]: chronic thyroiditis with transient thyrotoxicosis (E06.2)
- E06.3 Autoimmune thyroiditis
- E07.1 Dyshormogenetic goiter
- E08.36 Diabetes mellitus due to underlying condition with diabetic cataract
- H28 Cataract in diseases classified elsewhere: cataract in diabetes mellitus (E08.36, E09.36, E10.36, E11.36, E13.36)
- H36 Retinal disorders in diseases classified elsewhere: diabetic retinopathy (E08.3-, E09.3-, E10.3-, E11.3-, E13.3-)
- E08.649 Diabetes mellitus due to underlying condition with hypoglycemia without coma
- E09 Drug or chemical induced diabetes mellitus: diabetes mellitus due to underlying condition (E08.-)
- E10 Type 1 diabetes mellitus: diabetes mellitus due to underlying condition (E08.-)
- E11 Type 2 diabetes mellitus: diabetes mellitus due to underlying condition (E08.-)
- E13 Other specified diabetes mellitus: diabetes mellitus due to underlying condition (E08.-)
- E87.2 Acidosis: diabetic acidosis - see categories E08-E10, E11, E13 with ketoacidosis
- E08-E13 Diabetes mellitus due to underlying condition to Other specified diabetes mellitus 432 codes
- E74 Other disorders of carbohydrate metabolism: diabetes mellitus (E08-E13)
- G54.5 Neuralgic amyotrophy: neuralgic amyotrophy in diabetes mellitus (E08-E13 with .44)
- G59 Mononeuropathy in diseases classified elsewhere: diabetic mononeuropathy (E08-E13 with .41)
- G63 Polyneuropathy in diseases classified elsewhere: diabetes mellitus (E08-E13 with .42)
- G99.0 Autonomic neuropathy in diseases classified elsewhere: diabetic autonomic neuropathy (E08-E13 with .43)
- H20.0 Acute and subacute iridocyclitis: iridocyclitis, iritis, uveitis (due to) (in) diabetes mellitus (E08-E13 with .39)
- I73.8 Other specified peripheral vascular diseases: diabetic (peripheral) angiopathy (E08-E13 with .51-.52)
- I79.8 Other disorders of arteries, arterioles and capillaries in diseases classified elsewhere: diabetic (peripheral) angiopathy (E08-E13 with .51-.52)
- L92.1 Necrobiosis lipoidica, not elsewhere classified: necrobiosis lipoidica associated with diabetes mellitus (E08-E13 with .620)
- L99 Other disorders of skin and subcutaneous tissue in diseases classified elsewhere: skin disorders in diabetes (E08-E13 with .62-)
- M14 Arthropathies in other diseases classified elsewhere: diabetes mellitus (E08-E13 with .61-)
- M14.6 Charcot's joint: Charcôt's joint in diabetes mellitus (E08-E13 with .610)
- M90 Osteopathies in diseases classified elsewhere: diabetes mellitus (E08-E13 with .69-)
- N08 Glomerular disorders in diseases classified elsewhere: diabetes (E08-E13 with .21)
- N16 Renal tubulo-interstitial disorders in diseases classified elsewhere: renal tubular degeneration in diabetes (E08-E13 with .29)
- N76.82 Fournier disease of vagina and vulva: gangrene in diabetes mellitus (E08-E13 with .52)
- R40 Somnolence, stupor and coma: somnolence, stupor and coma in diabetes (E08-E13)
- R73 Elevated blood glucose level: diabetes mellitus (E08-E13)
- R73.0 Abnormal glucose: diabetes mellitus (E08-E13)
- E09.36 Drug or chemical induced diabetes mellitus with diabetic cataract
- H28 Cataract in diseases classified elsewhere: cataract in diabetes mellitus (E08.36, E09.36, E10.36, E11.36, E13.36)
- H36 Retinal disorders in diseases classified elsewhere: diabetic retinopathy (E08.3-, E09.3-, E10.3-, E11.3-, E13.3-)
- E09.649 Drug or chemical induced diabetes mellitus with hypoglycemia without coma
- E16.0 Drug-induced hypoglycemia without coma: diabetes with hypoglycemia without coma (E09.649)
- E08 Diabetes mellitus due to underlying condition: drug or chemical induced diabetes mellitus (E09.-)
- E10 Type 1 diabetes mellitus: drug or chemical induced diabetes mellitus (E09.-)
- E11 Type 2 diabetes mellitus: drug or chemical induced diabetes mellitus (E09.-)
- E13 Other specified diabetes mellitus: drug or chemical induced diabetes mellitus (E09.-)
- E10.36 Type 1 diabetes mellitus with diabetic cataract
- H28 Cataract in diseases classified elsewhere: cataract in diabetes mellitus (E08.36, E09.36, E10.36, E11.36, E13.36)
- H36 Retinal disorders in diseases classified elsewhere: diabetic retinopathy (E08.3-, E09.3-, E10.3-, E11.3-, E13.3-)
- E10.649 Type 1 diabetes mellitus with hypoglycemia without coma
- R73.0 Abnormal glucose: type 1 diabetes mellitus, presymptomatic (E10.A-)
- E08 Diabetes mellitus due to underlying condition: type 1 diabetes mellitus (E10.-)
- E09 Drug or chemical induced diabetes mellitus: type 1 diabetes mellitus (E10.-)
- E11 Type 2 diabetes mellitus: type 1 diabetes mellitus (E10.-)
- E13 Other specified diabetes mellitus: diabetes (mellitus) due to autoimmune process (E10.-)
- E13 Other specified diabetes mellitus: diabetes (mellitus) due to immune mediated pancreatic islet beta-cell destruction (E10.-)
- E13 Other specified diabetes mellitus: type 1 diabetes mellitus (E10.-)
- Q45.3 Other congenital malformations of pancreas and pancreatic duct: congenital diabetes mellitus (E10.-)
- E11.0-E11.8 Type 2 diabetes mellitus with hyperosmolarity to Type 2 diabetes mellitus with unspecified complications 85 codes
- E11.A Type 2 diabetes mellitus without complications in remission: type 2 diabetes mellitus, with complications (E11.0-E11.8)
- E11.36 Type 2 diabetes mellitus with diabetic cataract
- H28 Cataract in diseases classified elsewhere: cataract in diabetes mellitus (E08.36, E09.36, E10.36, E11.36, E13.36)
- H36 Retinal disorders in diseases classified elsewhere: diabetic retinopathy (E08.3-, E09.3-, E10.3-, E11.3-, E13.3-)
- E11.649 Type 2 diabetes mellitus with hypoglycemia without coma
- E11.9 Type 2 diabetes mellitus without complications
- E11.A Type 2 diabetes mellitus without complications in remission: type 2 diabetes mellitus, without complications not in remission (E11.9)
- E11.A Type 2 diabetes mellitus without complications in remission
- E11.9 Type 2 diabetes mellitus without complications: type 2 diabetes mellitus, without complications in remission (E11.A)
- E08 Diabetes mellitus due to underlying condition: type 2 diabetes mellitus (E11.-)
- E09 Drug or chemical induced diabetes mellitus: type 2 diabetes mellitus (E11.-)
- E10 Type 1 diabetes mellitus: type 2 diabetes mellitus (E11.-)
- E87.2 Acidosis: diabetic acidosis - see categories E08-E10, E11, E13 with ketoacidosis
- E13.36 Other specified diabetes mellitus with diabetic cataract
- H28 Cataract in diseases classified elsewhere: cataract in diabetes mellitus (E08.36, E09.36, E10.36, E11.36, E13.36)
- H36 Retinal disorders in diseases classified elsewhere: diabetic retinopathy (E08.3-, E09.3-, E10.3-, E11.3-, E13.3-)
- E13.649 Other specified diabetes mellitus with hypoglycemia without coma
- E08 Diabetes mellitus due to underlying condition: postpancreatectomy diabetes mellitus (E13.-)
- E08 Diabetes mellitus due to underlying condition: postprocedural diabetes mellitus (E13.-)
- E08 Diabetes mellitus due to underlying condition: secondary diabetes mellitus NEC (E13.-)
- E09 Drug or chemical induced diabetes mellitus: postpancreatectomy diabetes mellitus (E13.-)
- E09 Drug or chemical induced diabetes mellitus: postprocedural diabetes mellitus (E13.-)
- E09 Drug or chemical induced diabetes mellitus: secondary diabetes mellitus NEC (E13.-)
- E10 Type 1 diabetes mellitus: postpancreatectomy diabetes mellitus (E13.-)
- E10 Type 1 diabetes mellitus: postprocedural diabetes mellitus (E13.-)
- E10 Type 1 diabetes mellitus: secondary diabetes mellitus NEC (E13.-)
- E11 Type 2 diabetes mellitus: postpancreatectomy diabetes mellitus (E13.-)
- E11 Type 2 diabetes mellitus: postprocedural diabetes mellitus (E13.-)
- E11 Type 2 diabetes mellitus: secondary diabetes mellitus NEC (E13.-)
- E87.2 Acidosis: diabetic acidosis - see categories E08-E10, E11, E13 with ketoacidosis
- E15 Nondiabetic hypoglycemic coma
- R40 Somnolence, stupor and coma: somnolence, stupor and coma in hypoglycemia (nondiabetic) (E15)
- E16.2 Hypoglycemia, unspecified
- E16.3 Increased secretion of glucagon
- E74 Other disorders of carbohydrate metabolism: increased secretion of glucagon (E16.3)
- E16.4 Increased secretion of gastrin
- K29 Gastritis and duodenitis: Zollinger-Ellison syndrome (E16.4)
- E16.8 Other specified disorders of pancreatic internal secretion
- E22.0 Acromegaly and pituitary gigantism: increased secretion from endocrine pancreas of growth hormone-releasing hormone (E16.8)
- E20.1 Pseudohypoparathyroidism
- E20.810 Autosomal dominant hypocalcemia
- E83.5 Disorders of calcium metabolism: autosomal dominant hypocalcemia (E20.810)
- E20.811 Secondary hypoparathyroidism in diseases classified elsewhere
- E83.5 Disorders of calcium metabolism: secondary hypoparathyroidism in diseases classified elsewhere (E20.811)
- E20.812 Autoimmune hypoparathyroidism
- E83.5 Disorders of calcium metabolism: autoimmune hypoparathyroidism (E20.812)
- E20.9 Hypoparathyroidism, unspecified
- R29.0 Tetany: parathyroid tetany (E20.9)
- E83 Disorders of mineral metabolism: parathyroid disorders (E20-E21)
- E21.0 Primary hyperparathyroidism
- M85.6 Other cyst of bone: osteitis fibrosa cystica generalisata [von Recklinghausen's disease of bone] (E21.0)
- E83.5 Disorders of calcium metabolism: hyperparathyroidism (E21.0-E21.3)
- E21.1 Secondary hyperparathyroidism, not elsewhere classified
- N25.81 Secondary hyperparathyroidism of renal origin: secondary hyperparathyroidism, non-renal (E21.1)
- E22.0 Acromegaly and pituitary gigantism
- M26.0 Major anomalies of jaw size: acromegaly (E22.0)
- E22.2 Syndrome of inappropriate secretion of antidiuretic hormone
- E87.1 Hypo-osmolality and hyponatremia: syndrome of inappropriate secretion of antidiuretic hormone (E22.2)
- E22.8 Other hyperfunction of pituitary gland
- E30.1 Precocious puberty: central precocious puberty (E22.8)
- E23.0 Hypopituitarism
- E28 Ovarian dysfunction: isolated gonadotropin deficiency (E23.0)
- E29 Testicular dysfunction: isolated gonadotropin deficiency (E23.0)
- E34.3 Short stature due to endocrine disorder: pituitary short stature (E23.0)
- R62 Lack of expected normal physiological development in childhood and adults: hypopituitarism (E23.0)
- E23.2 Diabetes insipidus
- E24.0 Pituitary-dependent Cushing's disease
- E22 Hyperfunction of pituitary gland: overproduction of pituitary ACTH (E24.0)
- E24.1 Nelson's syndrome
- E22 Hyperfunction of pituitary gland: Nelson's syndrome (E24.1)
- E24.3 Ectopic ACTH syndrome
- E34.2 Ectopic hormone secretion, not elsewhere classified: ectopic ACTH syndrome (E24.3)
- E25.0 Congenital adrenogenital disorders associated with enzyme deficiency
- E24 Cushing's syndrome: congenital adrenal hyperplasia (E25.0)
- E30.1 Precocious puberty: congenital adrenal hyperplasia (E25.0)
- Block E70-E88 Metabolic disorders: congenital adrenal hyperplasia (E25.0)
- Q89.1 Congenital malformations of adrenal gland: congenital adrenal hyperplasia (E25.0)
- E30.1 Precocious puberty: female heterosexual precocious pseudopuberty (E25.-)
- E30.1 Precocious puberty: male isosexual precocious pseudopuberty (E25.-)
- Q56 Indeterminate sex and pseudohermaphroditism: female pseudohermaphroditism with adrenocortical disorder (E25.-)
- Q89.1 Congenital malformations of adrenal gland: adrenogenital disorders (E25.-)
- E27.0 Other adrenocortical overactivity
- E22 Hyperfunction of pituitary gland: overproduction of ACTH not associated with Cushing's disease (E27.0)
- E28.2 Polycystic ovarian syndrome
- E28.310 Symptomatic premature menopause
- N95.1 Menopausal and female climacteric states: symptoms associated with premature menopause (E28.310)
- N91 Absent, scanty and rare menstruation: ovarian dysfunction (E28.-)
- E29.1 Testicular hypofunction
- Block E70-E88 Metabolic disorders: 5-alpha-reductase deficiency (E29.1)
- E30.0 Delayed puberty
- R62 Lack of expected normal physiological development in childhood and adults: delayed puberty (E30.0)
- E30.1 Precocious puberty
- D44 Neoplasm of uncertain behavior of endocrine glands: multiple endocrine adenomatosis (E31.2-)
- D44 Neoplasm of uncertain behavior of endocrine glands: multiple endocrine neoplasia (E31.2-)
- E31.1 Polyglandular hyperfunction: multiple endocrine adenomatosis (E31.2-)
- E31.1 Polyglandular hyperfunction: multiple endocrine neoplasia (E31.2-)
- Z15.81 Genetic susceptibility to multiple endocrine neoplasia [MEN]: multiple endocrine neoplasia [MEN] syndromes (E31.2-)
- E34.2 Ectopic hormone secretion, not elsewhere classified
- E21 Hyperparathyroidism and other disorders of parathyroid gland: ectopic hyperparathyroidism (E34.2)
- E34.4 Constitutional tall stature
- E29 Testicular dysfunction: androgen insensitivity syndrome (E34.5-)
- Block E70-E88 Metabolic disorders: androgen insensitivity syndrome (E34.5-)
- Block Q50-Q56 Congenital malformations of genital organs: androgen insensitivity syndrome (E34.5-)
- Q56 Indeterminate sex and pseudohermaphroditism: androgen insensitivity syndrome (E34.5-)
- E34.8 Other specified endocrine disorders
- E36.1- Accidental puncture and laceration of an endocrine system organ or structure during a procedure 2 codes
- E36.0 Intraoperative hemorrhage and hematoma of an endocrine system organ or structure complicating a procedure: intraoperative hemorrhage and hematoma of an endocrine system organ or structure due to accidental puncture or laceration during a procedure (E36.1-)
- R63.6 Underweight: malnutrition (E40-E46)
- Z72.4 Inappropriate diet and eating habits: malnutrition and other nutritional deficiencies (E40-E64)
- E41 Nutritional marasmus
- E42 Marasmic kwashiorkor
- E45 Retarded development following protein-calorie malnutrition
- E50.0 Vitamin A deficiency with conjunctival xerosis
- H11.14 Conjunctival xerosis, unspecified: xerosis of conjunctiva due to vitamin A deficiency (E50.0, E50.1)
- E50.1 Vitamin A deficiency with Bitot's spot and conjunctival xerosis
- H11.14 Conjunctival xerosis, unspecified: xerosis of conjunctiva due to vitamin A deficiency (E50.0, E50.1)
- E50.4 Vitamin A deficiency with keratomalacia
- H18.44 Keratomalacia: keratomalacia due to vitamin A deficiency (E50.4)
- E50.5 Vitamin A deficiency with night blindness
- E50.8 Other manifestations of vitamin A deficiency
- T45.2X6 Underdosing of vitamins: vitamin deficiencies (E50-E56)
- E51.2 Wernicke's encephalopathy
- G32.8 Other specified degenerative disorders of nervous system in diseases classified elsewhere: superior hemorrhagic polioencephalitis [Wernicke's encephalopathy] (E51.2)
- E53.0 Riboflavin deficiency
- E53.8 Deficiency of other specified B group vitamins
- E54 Ascorbic acid deficiency
- D53.2 Scorbutic anemia: scurvy (E54)
- E55.0 Rickets, active
- E83 Disorders of mineral metabolism: vitamin D deficiency (E55.-)
- E56.1 Deficiency of vitamin K
- T45.7X6 Underdosing of anticoagulant antagonist, vitamin K and other coagulants: vitamin K deficiency (E56.1)
- E61.1 Iron deficiency
- T45.4X6 Underdosing of iron and its compounds: iron deficiency (E61.1)
- E63.9 Nutritional deficiency, unspecified
- E46 Unspecified protein-calorie malnutrition: nutritional deficiency NOS (E63.9)
- E64.0 Sequelae of protein-calorie malnutrition
- Block E40-E46 Malnutrition: sequelae of protein-calorie malnutrition (E64.0)
- E64.1 Sequelae of vitamin A deficiency
- E50 Vitamin A deficiency: sequelae of vitamin A deficiency (E64.1)
- E64.2 Sequelae of vitamin C deficiency
- E54 Ascorbic acid deficiency: sequelae of vitamin C deficiency (E64.2)
- E64.3 Sequelae of rickets
- E64.8 Sequelae of other nutritional deficiencies
- E51 Thiamine deficiency: sequelae of thiamine deficiency (E64.8)
- E52 Niacin deficiency [pellagra]: sequelae of niacin deficiency (E64.8)
- E53 Deficiency of other B group vitamins: sequelae of vitamin B deficiency (E64.8)
- E56 Other vitamin deficiencies: sequelae of other vitamin deficiencies (E64.8)
- E58 Dietary calcium deficiency: sequelae of calcium deficiency (E64.8)
- E59 Dietary selenium deficiency: sequelae of selenium deficiency (E64.8)
- E61 Deficiency of other nutrient elements: sequelae of malnutrition and other nutritional deficiencies (E64.-)
- E65 Localized adiposity
- R22 Localized swelling, mass and lump of skin and subcutaneous tissue: localized adiposity (E65)
- E66.2 Morbid (severe) obesity with alveolar hypoventilation
- R63.5 Abnormal weight gain: obesity (E66.-)
- E68 Sequelae of hyperalimentation
- E67 Other hyperalimentation: sequelae of hyperalimentation (E68)
- Q15 Other congenital malformations of eye: ocular albinism (E70.31-)
- E70.330 Chediak-Higashi syndrome
- E70.331 Hermansky-Pudlak syndrome
- E70.32 Oculocutaneous albinism: Hermansky-Pudlak syndrome (E70.331)
- E70.5 Disorders of tryptophan metabolism
- E72.0 Disorders of amino-acid transport: disorders of tryptophan metabolism (E70.5)
- E72 Other disorders of amino-acid metabolism: aromatic amino-acid metabolism (E70.-)
- E70-E72 Disorders of aromatic amino-acid metabolism to Other disorders of amino-acid metabolism 95 codes
- R79 Other abnormal findings of blood chemistry: specific findings indicating disorder of amino-acid metabolism (E70-E72)
- R79.83 Abnormal findings of blood amino-acid level: disorders of amino-acid metabolism (E70-E72)
- Block R80-R82 Abnormal findings on examination of urine, without diagnosis: specific findings indicating disorder of amino-acid metabolism (E70-E72)
- E70-E88 Disorders of aromatic amino-acid metabolism to Other and unspecified metabolic disorders 286 codes
- P59 Neonatal jaundice from other and unspecified causes: jaundice due to inborn errors of metabolism (E70-E88)
- E71.0-E71.2 Maple-syrup-urine disease to Disorder of branched-chain amino-acid metabolism, unspecified 9 codes
- E72 Other disorders of amino-acid metabolism: branched-chain amino-acid metabolism (E71.0-E71.2)
- E71.313 Glutaric aciduria type II
- E72.3 Disorders of lysine and hydroxylysine metabolism: glutaric aciduria type II (E71.313)
- E71.314 Muscle carnitine palmitoyltransferase deficiency
- E71.4 Disorders of carnitine metabolism: Muscle carnitine palmitoyltransferase deficiency (E71.314)
- E72 Other disorders of amino-acid metabolism: fatty-acid metabolism (E71.3)
- E71.42- Carnitine deficiency due to inborn errors of metabolism
- E71.511 Neonatal adrenoleukodystrophy: X-linked adrenoleukodystrophy (E71.42-)
- E71.510 Zellweger syndrome
- E71.528 Other X-linked adrenoleukodystrophy
- G37.0 Diffuse sclerosis of central nervous system: X linked adrenoleukodystrophy (E71.52-)
- E71.540 Rhizomelic chondrodysplasia punctata
- Q77.3 Chondrodysplasia punctata: Rhizomelic chondrodysplasia punctata (E71.540)
- E71.3 Disorders of fatty-acid metabolism: peroxisomal disorders (E71.5)
- E72.01 Cystinuria
- E72.1 Disorders of sulfur-bearing amino-acid metabolism: cystinuria (E72.01)
- E72.04 Cystinosis
- E72.09 Other disorders of amino-acid transport
- E72.04 Cystinosis: Fanconi (-de Toni) (-Debré) syndrome without cystinosis (E72.09)
- E72.11 Homocystinuria
- D68.6 Other thrombophilia: hyperhomocysteinemia (E72.11)
- E72.3 Disorders of lysine and hydroxylysine metabolism
- E71.313 Glutaric aciduria type II: glutaric aciduria (type 1) NOS (E72.3)
- E72.4 Disorders of ornithine metabolism
- Z91.011 Allergy to milk products: lactose intolerance (E73.-)
- R79 Other abnormal findings of blood chemistry: specific findings indicating disorder of carbohydrate metabolism (E73-E74)
- Block R80-R82 Abnormal findings on examination of urine, without diagnosis: specific findings indicating disorder of carbohydrate metabolism (E73-E74)
- E74.09 Other glycogen storage disease
- E74.1 Disorders of fructose metabolism: muscle phosphofructokinase deficiency (E74.09)
- E74.4 Disorders of pyruvate metabolism and gluconeogenesis
- E88.4 Mitochondrial metabolism disorders: disorders of pyruvate metabolism (E74.4)
- E74.818 Other disorders of glucose transport
- R81 Glycosuria: renal glycosuria (E74.818)
- D55.2 Anemia due to disorders of glycolytic enzymes: disorders of glycolysis not associated with anemia (E74.81-)
- E78 Disorders of lipoprotein metabolism and other lipidemias: sphingolipidosis (E75.0-E75.3)
- E75.242 Niemann-Pick disease type C
- E78.7 Disorders of bile acid and cholesterol metabolism: Niemann-Pick disease type C (E75.242)
- E75.5 Other lipid storage disorders
- E78.2 Mixed hyperlipidemia: cerebrotendinous cholesterosis [van Bogaert-Scherer- Epstein] (E75.5)
- R79 Other abnormal findings of blood chemistry: specific findings indicating disorder of lipid metabolism (E75.-)
- E77.0-E77.1 Defects in post-translational modification of lysosomal enzymes to Defects in glycoprotein degradation 2 codes
- E75 Disorders of sphingolipid metabolism and other lipid storage disorders: mucolipidosis, types I-III (E77.0-E77.1)
- E78.2 Mixed hyperlipidemia
- M67 Other disorders of synovium and tendon: xanthomatosis localized to tendons (E78.2)
- E78.49 Other hyperlipidemia
- E78.2 Mixed hyperlipidemia: familial combined hyperlipidemia (E78.49)
- E78.72 Smith-Lemli-Opitz syndrome
- Q87.1 Congenital malformation syndromes predominantly associated with short stature: Smith-Lemli-Opitz syndrome (E78.72)
- E78.81 Lipoid dermatoarthritis
- M14 Arthropathies in other diseases classified elsewhere: lipoid dermatoarthritis (E78.81)
- E78.89 Other lipoprotein metabolism disorders
- L98.6 Other infiltrative disorders of the skin and subcutaneous tissue: hyalinosis cutis et mucosae (E78.89)
- E79.0 Hyperuricemia without signs of inflammatory arthritis and tophaceous disease
- R79 Other abnormal findings of blood chemistry: asymptomatic hyperuricemia (E79.0)
- E79.1 Lesch-Nyhan syndrome
- D53.0 Protein deficiency anemia: Lesch-Nyhan syndrome (E79.1)
- E72 Other disorders of amino-acid metabolism: purine and pyrimidine metabolism (E79.-)
- E80.0 Hereditary erythropoietic porphyria
- Q82 Other congenital malformations of skin: congenital erythropoietic porphyria (E80.0)
- E80.4 Gilbert syndrome
- Block P50-P61 Hemorrhagic and hematological disorders of newborn: Gilbert syndrome (E80.4)
- E80.5 Crigler-Najjar syndrome
- Block P50-P61 Hemorrhagic and hematological disorders of newborn: Crigler-Najjar syndrome (E80.5)
- P57.8 Other specified kernicterus: Crigler-Najjar syndrome (E80.5)
- E80.6 Other disorders of bilirubin metabolism
- Block P50-P61 Hemorrhagic and hematological disorders of newborn: Dubin-Johnson syndrome (E80.6)
- E83.09 Other disorders of copper metabolism
- Q84.1 Congenital morphological disturbances of hair, not elsewhere classified: Menkes' kinky hair syndrome (E83.09)
- E83.110 Hereditary hemochromatosis
- K74 Fibrosis and cirrhosis of liver: pigmentary cirrhosis (of liver) (E83.110)
- P78.84 Gestational alloimmune liver disease: hemochromatosis (E83.11-)
- E83.2 Disorders of zinc metabolism
- Q82 Other congenital malformations of skin: acrodermatitis enteropathica (E83.2)
- E83.31 Familial hypophosphatemia
- E83.32 Hereditary vitamin D-dependent rickets (type 1) (type 2)
- E55.0 Rickets, active: hereditary vitamin D-dependent rickets (E83.32)
- E83.59 Other disorders of calcium metabolism
- N20 Calculus of kidney and ureter: nephrocalcinosis (E83.59)
- E58 Dietary calcium deficiency: disorders of calcium metabolism (E83.5-)
- E83.81 Hungry bone syndrome
- E84.0 Cystic fibrosis with pulmonary manifestations
- E84.11 Meconium ileus in cystic fibrosis
- Q45.3 Other congenital malformations of pancreas and pancreatic duct: fibrocystic disease of pancreas (E84.-)
- E85.0 Non-neuropathic heredofamilial amyloidosis
- E27.1 Primary adrenocortical insufficiency: amyloidosis (E85.-)
- Block M60-M63 Disorders of muscles: myopathy in amyloidosis (E85.-)
- E86.0 Dehydration
- R68.2 Dry mouth, unspecified: dry mouth due to dehydration (E86.0)
- E87.71 Transfusion associated circulatory overload
- J95.87 Transfusion-associated dyspnea (TAD): transfusion associated circulatory overload (TACO) (E87.71)
- R77 Other abnormalities of plasma proteins: disorders of plasma-protein metabolism (E88.0-)
- G71.3 Mitochondrial myopathy, not elsewhere classified: mitochondrial metabolism disorders (E88.4.-)
- R73.0 Abnormal glucose: dysmetabolic syndrome X (E88.81-)
- E88.A Wasting disease (syndrome) due to underlying condition
- R64 Cachexia: cachexia due to underlying condition (E88.A)
- E89.0 Postprocedural hypothyroidism
- E03 Other hypothyroidism: postprocedural hypothyroidism (E89.0)
- E89.1 Postprocedural hypoinsulinemia
- R73 Elevated blood glucose level: postsurgical hypoinsulinemia (E89.1)
- E89.2 Postprocedural hypoparathyroidism
- E89.3 Postprocedural hypopituitarism
- E23 Hypofunction and other disorders of the pituitary gland: postprocedural hypopituitarism (E89.3)
- E89.41 Symptomatic postprocedural ovarian failure
- N95.1 Menopausal and female climacteric states: symptoms associated with artificial menopause (E89.41)
- E89.5 Postprocedural testicular hypofunction
- E29.1 Testicular hypofunction: postprocedural testicular hypofunction (E89.5)
The first view lists notes printed in this chapter (a note on a category or block applies to every code beneath it). The second lists codes of this chapter named by Excludes1 Notes anywhere in the Tabular List, including notes in other chapters.
Questions About Excludes1 Notes
What does an Excludes1 note mean?
An Excludes1 note means “NOT CODED HERE!”: the excluded code should never be used at the same time as the code above the note. It is used when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition (Section I.A.12.a). The FY 2027 Tabular List has 5,411 of them; 5,284 name other codes, with 5,710 references to 3,528 distinct codes, categories and ranges.
Is there any exception to an Excludes1 note?
Yes: when the two conditions are unrelated to each other. The Guidelines’ example is F45.8, whose Excludes1 note names sleep related teeth grinding (G47.63). A patient with psychogenic dysmenorrhea (an inclusion term of F45.8) and teeth grinding may have both codes reported. If it is not clear whether the conditions are related, query the provider.
Related References
Source: FY 2027 ICD-10-CM Tabular List (CMS and NCHS) and the ICD-10-CM Official Guidelines for Coding and Reporting FY 2027, Section I.A. ICD List is not affiliated with CMS or NCHS.