ICD-10 Chapter E
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Contents
1
E00-E35 - Endocrine diseases
1.1
(E00-E07) Thyroid gland / Thyroid hormone
1.2
(E10-E16) Pancreas / Insulin, glucagon
1.2.1
(E10-E14) Diabetes mellitus
1.2.2
(E15-E16) Other disorders of glucose regulation and pancreatic internal secretion
1.3
(E20-E21) Parathyroid gland / PTH
1.4
(E22-E23) Pituitary gland / ADH, oxytocin, GH, ACTH, TSH, LH, FSH, prolactin
1.5
(E24-E27) Adrenal gland / Aldosterone, cortisol, epinephrine, norepinephrine
1.6
(E28-E30) Gonads / Estrogen, androgens, testosterone, etc.
1.7
(E31-E35) Other
2
E40-68 - Nutritional diseases
2.1
(E40-E46) Malnutrition
2.2
(E50-E64) Other nutritional deficiencies
2.3
(E65-E68) Obesity and other hyperalimentation
3
E70-E90 - Metabolic diseases
3.1
(E70-E79) Metabolic disorders of proteins, fats, and carbohydrates
3.1.1
(E70-E72) Amino-acids
3.1.2
(E73-E74) Carbohydrates
3.1.3
(E75) Lipids
3.1.4
(E76-E78) Combinations
3.2
(E79-E90) Other metabolic disorders
4
See also
E00-E35 - Endocrine diseases
(E00-E07) Thyroid gland / Thyroid hormone
(
E
00.
)
Congenital iodine-deficiency syndrome
(
E
01.
)
Iodine-deficiency
-related
thyroid
disorders and allied conditions
(
E
01.0
)
Iodine-deficiency-related diffuse (endemic) goitre
(
E
01.1
)
Iodine-deficiency-related multinodular (endemic) goitre
(
E
01.2
)
Iodine-deficiency-related (endemic) goitre, unspecified
(
E
01.8
) Other
iodine-deficiency
-related
thyroid
disorders and allied condition
(
E
02.
)
Subclinical
iodine-deficiency
hypothyroidism
(
E
03.
) Other
hypothyroidism
(
E
03.0
)
Congenital hypothyroidism
with
diffuse goitre
(
E
03.1
)
Congenital hypothyroidism
without
goitre
(
E
03.2
)
Hypothyroidism
due to
medicaments
and other
exogenous
substances
(
E
03.3
)
Postinfectious
hypothyroidism
(
E
03.4
)
Atrophy
of
thyroid
(acquired)
(
E
03.5
)
Myxoedema coma
(
E
04.
) Other nontoxic
goitre
(
E
05.
)
Thyrotoxicosis
(
hyperthyroidism
)
(
E
05.0
)
Thyrotoxicosis
with
diffuse goitre
Graves' disease
(
E
05.1
)
Thyrotoxicosis
with
toxic single thyroid nodule
(
E
05.2
)
Thyrotoxicosis
with
toxic multinodular goitre
(
E
05.3
)
Thyrotoxicosis
from
ectopic thyroid tissue
(
E
05.4
)
Thyrotoxicosis factitia
(
E
05.5
)
Thyroid crisis or storm
(
E
05.8
) Other
thyrotoxicosis
(
E
05.9
)
Thyrotoxicosis
, unspecified
(
E
06.
)
Thyroiditis
(
E
06.0
)
Acute
thyroiditis
(
E
06.1
)
Subacute
thyroiditis
De Quervain's thyroiditis
(
E
06.2
)
Chronic
thyroiditis
with
transient
thyrotoxicosis
(
E
06.3
)
Autoimmune
thyroiditis
Hashimoto's thyroiditis
(
E
06.4
)
Drug-induced
thyroiditis
(
E
06.5
) Other
chronic
thyroiditis
Riedel's thyroiditis
(
E
06.9
)
Thyroiditis
, unspecified
(
E
07.
) Other disorders of
thyroid
(
E
07.0
)
Hypersecretion of calcitonin
(
E
07.1
)
Dyshormogenetic goitre
(
E
07.8
) Other specified disorders of
thyroid
Sick-euthyroid syndrome
(
E
07.9
) Disorder of
thyroid
, unspecified
(E10-E16) Pancreas / Insulin, glucagon
(E10-E14) Diabetes mellitus
Note: the following conditions are subtypes of each code from E10-14:
(E1x.0)
Diabetic coma
(E1x.1)
Diabetic ketoacidosis
(E1x.2)
Diabetic nephropathy
(E1x.3)
Diabetic retinopathy
(E1x.4)
Diabetic neuropathy
(E1x.5)
Diabetic angiopathy
(E1x.6)
Diabetic arthropathy
(
E
10.
)
Insulin-dependent diabetes mellitus
(
E
11.
)
Non-insulin-dependent diabetes mellitus
(
E
12.
)
Malnutrition
-related
diabetes mellitus
(
E
13.
) Other specified
diabetes mellitus
(
E
14.
) Unspecified
diabetes mellitus
(E15-E16) Other disorders of glucose regulation and pancreatic internal secretion
(
E
15.
)
Nondiabetic hypoglycaemic coma
Drug-induced insulin coma in nondiabetic
Hyperinsulinism
with
hypoglycaemic coma
Hypoglycaemic coma
NOS
(
E
16.
) Other disorders of
pancreatic internal secretion
(
E
16.0
)
Drug-induced hypoglycaemia
without
coma
(
E
16.1
) Other
hypoglycaemia
Functional nonhyperinsulinaemic hypoglycaemia
Hyperinsulinism
: NOS
Hyperinsulinism
: functional
Hyperplasia of pancreatic islet beta cells
NOS
Posthypoglycaemic coma encephalopathy
(
E
16.2
)
Hypoglycaemia
, unspecified
(
E
16.3
) Increased secretion of
glucagon
(
E
16.4
) Abnormal secretion of
gastrin
Hypergastrinaemia
Zollinger-Ellison syndrome
(
E
16.8
) Other specified disorders of
pancreatic internal secretion
(
E
16.9
) Disorder of
pancreatic internal secretion
, unspecified
(E20-E21) Parathyroid gland / PTH
(
E
20.
)
Hypoparathyroidism
(
E
20.0
)
Idiopathic
hypoparathyroidism
(
E
20.1
)
Pseudohypoparathyroidism
(
E
21.
)
Hyperparathyroidism
and other disorders of
parathyroid gland
(
E
21.0
)
Primary hyperparathyroidism
(
E
21.1
)
Secondary hyperparathyroidism
, not elsewhere classified
(E22-E23) Pituitary gland / ADH, oxytocin, GH, ACTH, TSH, LH, FSH, prolactin
(
E
22.
)
Hyperfunction
of
pituitary gland
(
E
22.0
)
Acromegaly
and
pituitary gigantism
(
E
22.1
)
Hyperprolactinaemia
(
E
22.2
)
Syndrome of inappropriate secretion of antidiuretic hormone
Central
precocious puberty
(
E
23.
)
Hypofunction
and other disorders of
pituitary gland
(
E
23.0
)
Hypopituitarism
Fertile eunuch syndrome
Hypogonadotropic hypogonadism
Idiopathic growth hormone deficiency
Isolated deficiency of
gonadotropin
Isolated deficiency of
growth hormone
Isolated deficiency of
pituitary hormone
Kallmann's syndrome
Lorain-Levi short stature
Necrosis
of
pituitary gland
(
postpartum
)
Panhypopituitarism
Pituitary
cachexia
Pituitary insufficiency
NOS
Pituitary
short stature
Sheehan's syndrome
Simmonds' disease
(
E
23.1
)
Drug-induced
hypopituitarism
(
E
23.2
)
Diabetes insipidus
(
E
23.3
)
Hypothalamic dysfunction
, not elsewhere classified
(
E
23.6
) Other disorders of
pituitary gland
Abscess of pituitary
Adiposogenital dystrophy
(
E
23.7
) Disorder of
pituitary gland
, unspecified
(E24-E27) Adrenal gland / Aldosterone, cortisol, epinephrine, norepinephrine
(
E
24.
)
Cushing's syndrome
(
E
24.0
)
Pituitary-dependent Cushing's disease
(
E
24.1
)
Nelson's syndrome
(
E
24.2
)
Ectopic ACTH syndrome
(
E
24.3
)
Alcohol
-induced
pseudo-Cushing's syndrome
(
E
24.4
) Other
Cushing's syndrome
(
E
24.5
)
Cushing's syndrome
, unspecified
(
E
25.
)
Adrenogenital disorders
(
E
25.0
)
Congenital adrenogenital disorders
associated with
enzyme deficiency
Congenital adrenal hyperplasia
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency
(
E
26.
)
Hyperaldosteronism
(
E
26.0
)
Primary hyperaldosteronism
Conn's syndrome
Primary aldosteronism due to adrenal hyperplasia
(bilateral)
(
E
26.1
)
Secondary hyperaldosteronism
(
E
26.8
) Other
hyperaldosteronism
Bartter's syndrome
(
E
26.9
)
Hyperaldosteronism
, unspecified
(
E
27.
) Other disorders of
adrenal gland
(
E
27.0
) Other
adrenocortical
overactivity
(
E
27.1
)
Primary adrenocortical insufficiency
Addison's disease
(
E
27.2
)
Addisonian crisis
(
E
27.3
)
Drug-induced
adrenocortical insufficiency
(
E
27.4
) Other and unspecified
adrenocortical insufficiency
Hypoaldosteronism
Adrenocortical insufficiency
NOS
(
E
27.5
)
Adrenomedullary
hyperfunction
(E28-E30) Gonads / Estrogen, androgens, testosterone, etc.
(
E
28.
)
Ovarian
dysfunction
(
E
28.0
)
Estrogen
excess
(
E
28.1
)
Androgen
excess
(
E
28.2
)
Polycystic ovarian syndrome
(
E
28.3
)
Primary ovarian failure
Premature menopause
NOS
(
E
29.
)
Testicular
dysfunction
(
E
29.0
)
Testicular hyperfunction
(
E
29.1
)
Testicular hypofunction
5-Alpha-reductase deficiency
(with male
pseudohermaphroditism
)
Testicular hypogonadism
NOS
(
E
30.
) Disorders of
puberty
, not elsewhere classified
(
E
30.0
)
Delayed puberty
(
E
30.1
)
Precocious puberty
(
E
30.8
) Other disorders of
puberty
Premature
thelarche
(E31-E35) Other
(
E
31.
)
Polyglandular
dysfunction
(
E
31.0
)
Autoimmune
polyglandular
failure
Schmidt's syndrome
(
E
31.1
)
Polyglandular
hyperfunction
(
E
32.
) Diseases of
thymus
(
E
32.0
)
Persistent hyperplasia of thymus
Hypertrophy of thymus
(
E
32.1
)
Abscess of thymus
(
E
34.
) Other
endocrine disorders
(
E
34.0
)
Carcinoid syndrome
(
E
34.1
) Other
hypersecretion
of
intestinal hormones
(
E
34.2
)
Ectopic hormone secretion
, not elsewhere classified
(
E
34.3
)
Short stature
, not elsewhere classified
NOS
constitutional
Laron-type
psychosocial
(
E
34.4
)
Constitutional tall stature
Constitutional
gigantism
(
E
34.5
)
Androgen resistance syndrome
Reifenstein's syndrome
(
E
34.8
) Other specified
endocrine
disorders
Progeria
(
E
35.
) Disorders of
endocrine glands
in diseases classified elsewhere
(
E
35.0
) Disorders of
thyroid gland
in diseases classified elsewhere
(
E
35.1
) Disorders of
adrenal glands
in diseases classified elsewhere
(
E
35.8
) Disorders of other
endocrine glands
in diseases classified elsewhere
E40-68 - Nutritional diseases
(E40-E46) Malnutrition
(
E
40.
)
Kwashiorkor
(
E
41.
)
Nutritional
marasmus
(
E
42.
)
Marasmic
kwashiorkor
(
E
43.
) Unspecified severe
protein-energy malnutrition
(
E
44.
)
Protein-energy malnutrition
of moderate and mild degree
(
E
45.
)
Retarded development
following
protein-energy malnutrition
(
E
46.
) Unspecified
protein-energy malnutrition
(E50-E64) Other nutritional deficiencies
(
E
50.
)
Vitamin A
deficiency
(
E
50.0
)
Vitamin A
deficiency with
conjunctival
xerosis
(
E
50.1
)
Vitamin A
deficiency with
Bitot's spot
and
conjunctival
xerosis
(
E
50.2
)
Vitamin A
deficiency with
corneal
xerosis
(
E
50.3
)
Vitamin A
deficiency with
corneal
ulceration
and
xerosis
(
E
50.4
)
Vitamin A
deficiency with
keratomalacia
(
E
50.5
)
Vitamin A
deficiency with
night blindness
(
E
50.6
)
Vitamin A
deficiency with
xerophthalmic
scars of
cornea
(
E
50.7
) Other ocular manifestations of
vitamin A
deficiency
Xerophthalmia
NOS
(
E
51.
)
Thiamine
deficiency
(
E
51.1
)
Beriberi
(
E
51.2
)
Wernicke's encephalopathy
(
E
52.
)
Niacin
deficiency (
pellagra
)
(
E
53.
) Deficiency of other
B group vitamins
(
E
53.0
)
Riboflavin
deficiency
Ariboflavinosis
(
E
53.1
)
Pyridoxine
deficiency
(
E
53.8
) Deficiency of other specified
B group vitamins
(
E
54.
)
Ascorbic acid
deficiency
Scurvy
(
E
55.
)
Vitamin D deficiency
(
E
55.0
)
Rickets
, active
(
E
56.
) Other
vitamin
deficiencies
(
E
56.0
) Deficiency of
vitamin E
(
E
56.1
) Deficiency of
vitamin K
(
E
58.
) Dietary
calcium deficiency
(
E
59.
) Dietary
selenium deficiency
(
E
60.
) Dietary
zinc deficiency
(
E
61.
) Deficiency of other
nutrient
elements
(
E
61.1
)
Iron deficiency
(
E
61.2
)
Magnesium deficiency
(
E
61.3
)
Manganese deficiency
(
E
61.4
)
Chromium deficiency
(
E
61.5
)
Molybdenum deficiency
(
E
61.6
)
Vanadium deficiency
(
E
63.
) Other
nutritional deficiencies
(
E
63.0
)
Essential fatty acid
(EFA) deficiency
(
E
64.
)
Sequelae
of
malnutrition
and other
nutritional deficiencies
(E65-E68) Obesity and other hyperalimentation
(
E
65.
)
Localized
adiposity
Fat pad
(
E
66.
)
Obesity
(
E
66.0
)
Obesity due to excess calories
(
E
66.1
)
Drug-induced obesity
(
E
66.2
)
Extreme obesity
with
alveolar hypoventilation
Pickwickian syndrome
(
E
66.8
) Other
obesity
Morbid obesity
(
E
66.9
)
Obesity
, unspecified
(
E
67.
) Other
hyperalimentation
(
E
67.0
)
Hypervitaminosis A
(
E
67.1
)
Hypercarotenaemia
(
E
67.2
)
Megavitamin-B 6 syndrome
(
E
67.3
)
Hypervitaminosis D
(
E
68.
)
Sequelae
of
hyperalimentation
E70-E90 - Metabolic diseases
(E70-E79) Metabolic disorders of proteins, fats, and carbohydrates
(E70-E72) Amino-acids
(
E
70.
) Disorders of
aromatic amino-acid
metabolism
(
E
70.0
) Classical
phenylketonuria
(
E
70.1
) Other
hyperphenylalaninaemias
(
E
70.2
) Disorders of
tyrosine
metabolism
Alkaptonuria
(
ILDS
E70.210)
Ochronosis
(
ILDS
E70.230)
Tyrosinaemia
(
E
70.3
)
Albinism
Oculocutaneous albinism
(
ILDS
E70.310)
Partial albinism
(
ILDS
E70.312)
Oculocutaneous albinism
type 1 (
tyrosinase
-negative) (
ILDS
E70.314)
Oculocutaneous albinism
type 2 (
tyrosinase
positive) (
ILDS
E70.314)
Albinoidism
(
ILDS
E70.318)
Waardenburg's syndrome
(
ILDS
E70.320)
Chediak-Higashi syndrome
(
ILDS
E70.340)
Piebaldism
(
ILDS
E70.350)
Tietz's syndrome
(
ILDS
E70.358)
Hermansky-Pudlak syndrome
(
ILDS
E70.360)
Cross syndrome
(
ILDS
E70.380)
(
E
70.8
) Other disorders of aromatic amino-acid metabolism
Disorders of
histidine
metabolism
Disorders of
tryptophan
metabolism
(
E
70.9
) Disorder of aromatic amino-acid metabolism, unspecified
(
E
71.
) Disorders of
branched-chain amino-acid
metabolism
and
fatty-acid metabolism
(
E
71.0
)
Maple-syrup-urine disease
(
E
71.1
) Other disorders of
branched-chain amino-acid
metabolism
Propionic acidemia
Methylmalonic acidemia
Isovaleric acidemia
(
E
71.2
) Disorder of
branched-chain amino-acid
metabolism
, unspecified
(
E
71.3
)
Disorders of fatty-acid metabolism
Adrenoleukodystrophy
(Addison-Schilder)
Muscle carnitine palmityltransferase deficiency
(
E
72.
) Other disorders of
amino-acid metabolism
(
E
72.0
) Disorders of
amino-acid
transport
Cystinuria
Cystinosis
Hartnup disease
Lowe's syndrome
(
E
72.1
) Disorders of
sulfur-bearing
amino-acid metabolism
Cystathioninuria
Homocystinuria
Methioninaemia
Sulfite oxidase deficiency
(
E
72.2
) Disorders of
urea cycle
metabolism
Argininaemia
Argininosuccinic aciduria
Citrullinaemia
Hyperammonaemia
(
E
72.3
) Disorders of
lysine
and
hydroxylysine
metabolism
Glutaric aciduria
Hydroxylysinaemia
Hyperlysinaemia
Lysinuric protein intolerance
(
E
72.4
) Disorders of
ornithine
metabolism
Ornithinaemia
(types I, II)
(
E
72.5
) Disorders of
glycine
metabolism
Hyperhydroxyprolinaemia
Hyperprolinaemia
(types I, II)
Non-ketotic hyperglycinaemia
Sarcosinaemia
(E73-E74) Carbohydrates
(
E
73.
)
Lactose intolerance
(
E
74.
) Other disorders of
carbohydrate metabolism
(
E
74.0
)
Glycogen storage disease
Glycogen storage disease type I
(
von Gierke's disease
)
Glycogen storage disease type II
(
Pompe's disease
)
Glycogen storage disease type III
Glycogen storage disease type IV
Glycogen storage disease type V
(
McArdle's disease
)
(
E
74.1
) Disorders of
fructose
metabolism
Essential fructosuria
Fructose-1,6-diphosphatase deficiency
Hereditary fructose intolerance
(
E
74.2
) Disorders of
galactose
metabolism
Galactosaemia
Galactokinase deficiency
(
E
74.3
) Other disorders of
intestinal carbohydrate absorption
Glucose-galactose malabsorption
Sucrase deficiency
(
E
74.4
) Disorders of
pyruvate metabolism
and
gluconeogenesis
Deficiency of phosphoenolpyruvate carboxykinase
Deficiency of pyruvate carboxylase
Deficiency of pyruvate dehydrogenase
(
E
74.8
) Other specified
disorders of carbohydrate metabolism
Essential pentosuria
Oxalosis
Oxaluria
Renal glycosuria
(
E
74.9
) Disorder of
carbohydrate metabolism
, unspecified
(E75) Lipids
(
E
75.
) Disorders of
sphingolipid
metabolism
and other
lipid storage
disorders
(
E
75.0
)
GM 2 gangliosidosis
Sandhoff disease
Tay-Sachs disease
(
E
75.1
) Other
gangliosidosis
GM 1
GM 3
Mucolipidosis IV
(
E
75.2
) Other
sphingolipidosis
Gaucher's disease
(
ILDS
E75.220)
Niemann-Pick disease
(
ILDS
E75.230)
Farber's disease
(
ILDS
E75.240)
Fabry's disease
(
ILDS
E75.250)
(
E
75.3
)
Sphingolipidosis
, unspecified
(
E
75.4
)
Neuronal ceroid lipofuscinosis
Batten disease
(Type 3)
Bielschowsky-Jansky disease
(Type 2)
Kufs disease
(Type 4)
Spielmeyer-Vogt disease
(Type 3)
(
E
75.5
) Other
lipid storage disorders
Cerebrotendinous cholesterosis
(van Bogaert-Scherer-Epstein)
Wolman's disease
(
E
75.6
)
Lipid storage disorder
, unspecified
(E76-E78) Combinations
(
E
76.
) Disorders of
glycosaminoglycan
metabolism
(
E
76.0
)
Mucopolysaccharidosis
, type I
Hurler syndrome
(
E
76.1
)
Mucopolysaccharidosis
, type II
Hunter syndrome
(
E
76.2
) Other
mucopolysaccharidoses
Sanfilippo syndrome
Morquio syndrome
(
E
77.
) Disorders of
glycoprotein
metabolism
(
E
77.0
) Defects in
