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ALL MEDICAL CODES IN CATEGORY Endocrine, nutritional and metabolic diseases (E00-E89)

2025 ICD-10-CM code E73

Lactose intolerance, or lactose malabsorption, is the inability to digest lactose, the sugar found in milk products. This is due to a lactase enzyme deficiency.

2025 ICD-10-CM code E25.8

Other adrenogenital disorders. This encompasses conditions where the adrenal glands produce abnormal levels of sex hormones and other adrenal hormones, not classified elsewhere.

2025 ICD-10-CM code E74

Other disorders of carbohydrate metabolism

2025 ICD-10-CM code E66.01

Morbid (severe) obesity due to excess calories.

2025 ICD-10-CM code E70.1

Other hyperphenylalaninemias. This refers to a rare inherited disorder of amino acid metabolism causing elevated blood phenylalanine levels (above 2 mg/dL but below 20 mg/dL), distinct from classical phenylketonuria (PKU).

2025 ICD-10-CM code E78

Disorders of lipoprotein metabolism and other lipidemias.

2025 ICD-10-CM code E24.1

Nelson's syndrome. This condition arises after bilateral adrenalectomy for Cushing's disease and involves excessive ACTH production by the pituitary gland.

2025 ICD-10-CM code E74.2

Disorders of galactose metabolism. This is a hereditary disorder of carbohydrate metabolism where the body cannot properly process galactose, a simple sugar found in many foods, especially dairy products.

2025 ICD-10-CM code E13.352

Other specified diabetes mellitus with proliferative diabetic retinopathy and traction retinal detachment involving the macula.

2025 ICD-10-CM code E70.310

X-linked ocular albinism (XLOA), a rare inherited eye disorder primarily affecting males, causing reduced pigmentation in the iris and retina.

2025 ICD-10-CM code E66.2

Morbid (severe) obesity with alveolar hypoventilation (Pickwickian syndrome).

2025 ICD-10-CM code E34.322

Insulin-like growth factor-1 (IGF-1) resistance, a genetic condition causing short stature.

2025 ICD-10-CM code E13.3521

Other specified diabetes mellitus with proliferative diabetic retinopathy and traction retinal detachment involving the macula of the right eye.

2025 ICD-10-CM code E71.313

Glutaricaciduria type II (GA2)

2025 ICD-10-CM code E13.3311

Other specified diabetes mellitus with moderate nonproliferative diabetic retinopathy and macular edema in the right eye.

2025 ICD-10-CM code E27.5

Adrenomedullary hyperfunction, also known as adrenomedullary hyperplasia or catecholamine hypersecretion, is the excessive production of adrenal hormones.

2025 ICD-10-CM code E23

Hypofunction and other disorders of the pituitary gland.

2025 ICD-10-CM code E32.9

Unspecified disease of the thymus gland.

2025 ICD-10-CM code E87.8

Other disorders of fluid and electrolyte balance, not elsewhere classified.

2025 ICD-10-CM code E70.320

Tyrosinase-negative oculocutaneous albinism (OCA1A), a genetic condition causing lack of melanin.

2025 ICD-10-CM code E74.29

Other disorders of galactose metabolism. This includes conditions such as galactokinase deficiency.

2025 ICD-10-CM code E13.3533

Other specified diabetes mellitus with proliferative diabetic retinopathy with traction retinal detachment not involving the macula, bilateral.

2025 ICD-10-CM code E76.210

Morquio A mucopolysaccharidoses. This is an inherited disorder primarily affecting the skeleton.

2025 ICD-10-CM code E05.31

Thyrotoxicosis from ectopic thyroid tissue with thyrotoxic crisis or storm.

2025 ICD-10-CM code E26.02

Glucocorticoid-remediable aldosteronism (GRA) is a type of primary hyperaldosteronism that is inherited. It typically appears before the age of 21 and leads to hypertension that can be managed with glucocorticoids like dexamethasone.

2025 ICD-10-CM code E64

This code represents the long-term complications or conditions resulting from malnutrition and other nutritional deficiencies.

2025 ICD-10-CM code E70.31

Ocular albinism. This condition primarily affects the eyes, reducing pigmentation in the iris and retina.

2025 ICD-10-CM code E30.9

Disorder of puberty, unspecified.

2025 ICD-10-CM code E05.21

Thyrotoxicosis with toxic multinodular goiter with thyrotoxic crisis or storm. This condition involves excessive thyroid hormone secretion due to an enlarged thyroid gland with multiple nodules, leading to a life-threatening state.

2025 ICD-10-CM code E36

Intraoperative complications of the endocrine system encompass various issues like hemorrhage, hematoma, puncture, and laceration of an endocrine organ or structure during a surgical procedure.

2025 ICD-10-CM code E50.3

Vitamin A deficiency with corneal ulceration and xerosis. This condition results from long-standing dietary deficiency of vitamin A, malabsorption of fat, or liver disorder.

2025 ICD-10-CM code E70.3

Albinism.

2025 ICD-10-CM code E78.89

This code represents other lipoprotein metabolism disorders, encompassing conditions not specifically classified elsewhere.

2025 ICD-10-CM code E71.110

Isovaleric acidemia, a rare genetic disorder characterized by the body's inability to break down the amino acid leucine.

2025 ICD-10-CM code E32.1

Abscess of thymus.

2025 ICD-10-CM code E87.21

Acute metabolic acidosis. This encompasses a rapid increase in acidity in the blood due to a buildup of acid or loss of bicarbonate.

2025 ICD-10-CM code E66.09

A condition characterized by excessive weight gain due to increased calorie consumption, beyond what is considered healthy.This code is used when the specific type of obesity due to excess calories is not otherwise specified.

2025 ICD-10-CM code E76.219

Morquio mucopolysaccharidoses, unspecified. This is a type of lysosomal storage disorder affecting the skeleton.

2025 ICD-10-CM code E70.39

Other specified albinism. This includes conditions like Piebaldism where there are symmetrical hypopigmented or depigmented patches of skin and a midline patch of white hair.

2025 ICD-10-CM code E51.8

Other manifestations of thiamine deficiency, a nutritional deficiency due to inadequate vitamin B1 intake.

2025 ICD-10-CM code E71.528

A rare genetic disorder primarily affecting males, characterized by the breakdown of myelin in the brain and spinal cord, and adrenal gland dysfunction.

2025 ICD-10-CM code E76.22

Sanfilippo mucopolysaccharidosis, also known as mucopolysaccharidosis type III (MPS III).

2025 ICD-10-CM code E78.8

A disorder characterized by the body's inability to process lipoproteins effectively, leading to abnormal levels of fats in the blood.

2025 ICD-10-CM code E79.8

This code refers to inherited metabolic disorders leading to excess uric acid (from purine breakdown) or excess ammonia, carbon dioxide, and beta-amino acids (from pyrimidine breakdown), causing various neurological, hematological, and immunological problems.

2025 ICD-10-CM code E13.3412

A specific type of diabetes mellitus characterized by severe nonproliferative diabetic retinopathy with macular edema affecting the left eye.

2025 ICD-10-CM code E71.32

Disorders of ketone metabolism are inborn errors of metabolism due to genetic defects affecting ketone body formation or breakdown, potentially leading to ketoacidosis.

2025 ICD-10-CM code E27.3

Drug-induced adrenocortical insufficiency, also known as secondary or exogenous adrenocortical insufficiency, is the underproduction of adrenal hormones (cortisol and sometimes aldosterone) due to drug-induced adrenal gland damage.

2025 ICD-10-CM code E10.3522

Type 1 diabetes mellitus with proliferative diabetic retinopathy with traction retinal detachment involving the macula, left eye.

2025 ICD-10-CM code E75.1

Other and unspecified gangliosidosis. This code is used for gangliosidoses other than GM2 gangliosidosis, or when the specific type of non-GM2 gangliosidosis is not specified.

2025 ICD-10-CM code E70.331

Hermansky-Pudlak syndrome