ICD-10-CM
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- E03.1 - Congenital hypothyroidism without goiter
- E03.4 - Atrophy of thyroid (acquired)
- E03.9 - Hypothyroidism, unspecified
- E04.0 - Nontoxic diffuse goiter
- E04.9 - Nontoxic goiter, unspecified
- E05.90 - Thyrotoxicosis, unspecified without thyrotoxic crisis or storm
- E06.0 - Acute thyroiditis
- E06.3 - Autoimmune thyroiditis
- E06.9 - Thyroiditis, unspecified
- E07.89 - Other specified disorders of thyroid
- E10.10 - Type 1 diabetes mellitus with ketoacidosis without coma
- E10.11 - Type 1 diabetes mellitus with ketoacidosis with coma
- E16.3 - Increased secretion of glucagon
- E16.4 - Increased secretion of gastrin
- E21.3 - Hyperparathyroidism, unspecified
- E22.0 - Acromegaly and pituitary gigantism
- E22.2 - Syndrome of inappropriate secretion of antidiuretic hormone
- E23.0 - Hypopituitarism
- E23.6 - Other disorders of pituitary gland
- E24.0 - Pituitary-dependent Cushing's disease
- E24.3 - Ectopic ACTH syndrome
- E25.0 - Congenital adrenogenital disorders associated with enzyme deficiency
- E25.8 - Other adrenogenital disorders
- E25.9 - Adrenogenital disorder, unspecified
- E26.02 - Glucocorticoid-remediable aldosteronism
- E26.09 - Other primary hyperaldosteronism
- E26.1 - Secondary hyperaldosteronism
- E26.81 - Bartter's syndrome
- E26.89 - Other hyperaldosteronism
- E26.9 - Hyperaldosteronism, unspecified
- E27.0 - Other adrenocortical overactivity
- E27.1 - Primary adrenocortical insufficiency
- E27.2 - Addisonian crisis
- E27.49 - Other adrenocortical insufficiency
- E27.8 - Other specified disorders of adrenal gland
- E28.8 - Other ovarian dysfunction
- E29.1 - Testicular hypofunction
- E30.1 - Precocious puberty
- E31.0 - Autoimmune polyglandular failure
- E31.20 - Multiple endocrine neoplasia [MEN] syndrome, unspecified
- E31.8 - Other polyglandular dysfunction
- E32.1 - Abscess of thymus
- E32.8 - Other diseases of thymus
- E34.0 - Carcinoid syndrome
- E34.50 - Androgen insensitivity syndrome, unspecified
- E34.8 - Other specified endocrine disorders
- E34.9 - Endocrine disorder, unspecified
- E35 - Disorders of endocrine glands in diseases classified elsewhere
- E41 - Nutritional marasmus
- E43 - Unspecified severe protein-calorie malnutrition
- E46 - Unspecified protein-calorie malnutrition
- E50.5 - Vitamin A deficiency with night blindness
- E51.11 - Dry beriberi
- E51.12 - Wet beriberi
- E51.9 - Thiamine deficiency, unspecified
- E52 - Niacin deficiency [pellagra]
- E53.0 - Riboflavin deficiency
- E53.1 - Pyridoxine deficiency
- E53.8 - Deficiency of other specified B group vitamins
- E53.9 - Vitamin B deficiency, unspecified
- E54 - Ascorbic acid deficiency
- E55.0 - Rickets, active
- E55.9 - Vitamin D deficiency, unspecified
- E56.1 - Deficiency of vitamin K
- E56.9 - Vitamin deficiency, unspecified
- E63.9 - Nutritional deficiency, unspecified
- E64.3 - Sequelae of rickets
- E65 - Localized adiposity
- E67.1 - Hypercarotenemia
- E70.29 - Other disorders of tyrosine metabolism
- E70.30 - Albinism, unspecified
- E70.310 - X-linked ocular albinism
- E70.311 - Autosomal recessive ocular albinism
- E70.318 - Other ocular albinism
- E70.319 - Ocular albinism, unspecified
- E70.320 - Tyrosinase negative oculocutaneous albinism
- E70.321 - Tyrosinase positive oculocutaneous albinism
- E70.328 - Other oculocutaneous albinism
- E70.329 - Oculocutaneous albinism, unspecified
- E70.330 - Chediak-Higashi syndrome
- E70.331 - Hermansky-Pudlak syndrome
- E70.338 - Other albinism with hematologic abnormality
- E70.339 - Albinism with hematologic abnormality, unspecified
- E70.39 - Other specified albinism
- E70.89 - Other disorders of aromatic amino-acid metabolism
- E70.9 - Disorder of aromatic amino-acid metabolism, unspecified
- E71.110 - Isovaleric acidemia
- E71.120 - Methylmalonic acidemia
- E71.121 - Propionic acidemia
- E71.2 - Disorder of branched-chain amino-acid metabolism, unspecified
- E71.313 - Glutaric aciduria type II
- E71.511 - Neonatal adrenoleukodystrophy
- E71.520 - Childhood cerebral X-linked adrenoleukodystrophy
- E71.521 - Adolescent X-linked adrenoleukodystrophy
- E71.522 - Adrenomyeloneuropathy
- E71.528 - Other X-linked adrenoleukodystrophy
- E71.529 - X-linked adrenoleukodystrophy, unspecified type
- E71.5 - Peroxisomal disorders
- E72.04 - Cystinosis
- E72.09 - Other disorders of amino-acid transport
- E72.21 - Argininemia
- E72.22 - Arginosuccinic aciduria
- E72.3 - Disorders of lysine and hydroxylysine metabolism
- E72.81 - Disorders of gamma aminobutyric acid metabolism
- E72.9 - Disorder of amino-acid metabolism, unspecified
- E73.0 - Congenital lactase deficiency
- E74.00 - Glycogen storage disease, unspecified
- E74.03 - Cori disease
- E74.09 - Other glycogen storage disease
- E75.21 - Fabry (-Anderson) disease
- E75.29 - Other sphingolipidosis
- E75.4 - Neuronal ceroid lipofuscinosis
- E77.1 - Defects in glycoprotein degradation
- E78.2 - Mixed hyperlipidemia
- E78.3 - Hyperchylomicronemia
- E78.6 - Lipoprotein deficiency
- E78.71 - Barth syndrome
- E78.81 - Lipoid dermatoarthritis
- E79.1 - Lesch-Nyhan syndrome
- E79.8 - Other disorders of purine and pyrimidine metabolism
- E80.3 - Defects of catalase and peroxidase
- E80.4 - Gilbert syndrome
- E80.6 - Other disorders of bilirubin metabolism
- E80.7 - Disorder of bilirubin metabolism, unspecified
- E83.118 - Other hemochromatosis
- E83.2 - Disorders of zinc metabolism
- E83.39 - Other disorders of phosphorus metabolism
- E83.50 - Unspecified disorder of calcium metabolism
- E83.52 - Hypercalcemia
- E83.59 - Other disorders of calcium metabolism
- E85.0 - Non-neuropathic heredofamilial amyloidosis
- E85.1 - Neuropathic heredofamilial amyloidosis
- E85.2 - Heredofamilial amyloidosis, unspecified
- E85.3 - Secondary systemic amyloidosis
- E85.4 - Organ-limited amyloidosis
- E85.81 - Light chain (AL) amyloidosis
- E85.82 - Wild-type transthyretin-related (ATTR) amyloidosis
- E85.89 - Other amyloidosis
- E85.9 - Amyloidosis, unspecified
- E86.0 - Dehydration
- E87.20 - Acidosis, unspecified
- E87.21 - Acute metabolic acidosis
- E87.22 - Chronic metabolic acidosis
- E87.29 - Other acidosis
- E87.3 - Alkalosis
- E87.4 - Mixed disorder of acid-base balance
- E88.09 - Other disorders of plasma-protein metabolism, not elsewhere classified
- E88.1 - Lipodystrophy, not elsewhere classified
- E88.2 - Lipomatosis, not elsewhere classified
- E88.89 - Other specified metabolic disorders
- E88.9 - Metabolic disorder, unspecified
- E89.0 - Postprocedural hypothyroidism
- E89.2 - Postprocedural hypoparathyroidism
- E89.3 - Postprocedural hypopituitarism
- E89.6 - Postprocedural adrenocortical (-medullary) hypofunction
- E89.89 - Other postprocedural endocrine and metabolic complications and disorders