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ALL MEDICAL CODES IN CATEGORY Endocrine, Nutritional and Metabolic Diseases (E00-E89)

2025 ICD-10-CM code E74.81

Disorders of glucose transport, not elsewhere classified.

2025 ICD-10-CM code E75.00

Unspecified GM2 gangliosidosis. This is a group of inherited lipid storage disorders caused by beta-hexosaminidase deficiency.

2025 ICD-10-CM code E56

A deficiency in vitamins other than those specifically classified elsewhere.

2025 ICD-10-CM code E28.319

Asymptomatic premature menopause. Cessation of menstruation before age 40 without related symptoms.

2025 ICD-10-CM code E10.610

Type 1 diabetes mellitus with diabetic neuropathic arthropathy. This condition involves joint damage due to nerve damage caused by diabetes.

2025 ICD-10-CM code E75.11

Mucolipidosis IV (ML4) is a rare lysosomal storage disorder. It primarily affects Ashkenazi Jews and is characterized by developmental delays, progressive vision impairment, and digestive issues.

2025 ICD-10-CM code E83.19

Other disorders of iron metabolism. Use additional code, if applicable, for idiopathic pulmonary hemosiderosis (J84.03).

2025 ICD-10-CM code E78.2

Mixed hyperlipidemia. This condition involves elevated levels of both cholesterol and triglycerides in the blood.

2025 ICD-10-CM code E53

Deficiency of other B group vitamins. This excludes sequelae of vitamin B deficiency (E64.8).

2025 ICD-10-CM code E25.9

Adrenogenital disorder, unspecified. This code is used when the specific type of adrenogenital disorder is not documented.

2025 ICD-10-CM code E80.0

Hereditary erythropoietic porphyria, also known as congenital erythropoietic porphyria or erythropoietic protoporphyria (EPP).

2025 ICD-10-CM code E08.34

Diabetes mellitus resulting from an underlying condition, complicated by severe nonproliferative diabetic retinopathy (NPDR).

2025 ICD-10-CM code E40

Kwashiorkor. Severe malnutrition with nutritional edema, skin and hair dyspigmentation.

2025 ICD-10-CM code E28.2

Polycystic ovarian syndrome (PCOS), also known as Stein-Leventhal syndrome or sclerocystic ovary syndrome.

2025 ICD-10-CM code E61.5

Molybdenum deficiency.

2025 ICD-10-CM code E75.3

Unspecified sphingolipidosis, a group of inherited disorders causing enzyme deficiencies and abnormal lipid metabolism, leading to lipid accumulation in the body.

2025 ICD-10-CM code E71.42

Carnitine deficiency due to inborn errors of metabolism. This is a genetic disorder characterized by the body's inability to process fatty acids due to insufficient carnitine or issues with its cellular transport.

2025 ICD-10-CM code E08.22

Diabetes mellitus due to an underlying condition with diabetic chronic kidney disease.

2025 ICD-10-CM code E50.1

Vitamin A deficiency with Bitot's spot and conjunctival xerosis.

2025 ICD-10-CM code E09.3539

Drug or chemical-induced diabetes mellitus with proliferative diabetic retinopathy with traction retinal detachment not involving the macula, unspecified eye.

2025 ICD-10-CM code E89.40

Asymptomatic postprocedural ovarian failure.The ovaries fail to produce eggs or hormones (estrogen or progesterone) after a procedure, but the patient has no symptoms.

2025 ICD-10-CM code E74.04

McArdle disease (also known as type 5 glycogen storage disease or GSD5) is a rare genetic disorder affecting carbohydrate metabolism. It is characterized by a deficiency of the enzyme glycogen phosphorylase, leading to glycogen accumulation in muscle cells.

2025 ICD-10-CM code E29.8

Other testicular dysfunction. This code represents any testicular dysfunction not otherwise specified in the ICD-10-CM.

2025 ICD-10-CM code E85.89

Other amyloidosis. This code is used for amyloidosis not otherwise specified in the ICD-10-CM.

2025 ICD-10-CM code E72.21

Argininemia is a genetic disorder characterized by the buildup of arginine in the blood due to a deficiency in the enzyme arginase, which is essential for breaking down arginine. This deficiency disrupts the urea cycle, a metabolic pathway that removes excess nitrogen from the body.

2025 ICD-10-CM code E78.71

Barth syndrome. A rare x-linked syndrome caused by mutations in the TAZ gene.

2025 ICD-10-CM code E75.29

This code represents a diagnosis of other sphingolipidosis, encompassing conditions not specifically classified elsewhere within the sphingolipidoses.

2025 ICD-10-CM code E89.81

Postprocedural hemorrhage of an endocrine system organ or structure following a procedure.

2025 ICD-10-CM code E87.7

Fluid overload.

2025 ICD-10-CM code E76.01

Hurler syndrome, a severe form of mucopolysaccharidosis type I (MPS I).

2025 ICD-10-CM code E85.4

Organ-limited amyloidosis is a condition characterized by the buildup of abnormal amyloid proteins in a single organ.

2025 ICD-10-CM code E74.39

Inability of the small intestines to break down and absorb carbohydrates.

2025 ICD-10-CM code E70.29

This code refers to other disorders of tyrosine metabolism, including alkaptonuria and ochronosis. It excludes transitory tyrosinemia of the newborn.

2025 ICD-10-CM code E71.520

Childhood cerebral X-linked adrenoleukodystrophy is a genetic disorder primarily affecting males, involving the nervous system and adrenal glands. It leads to deterioration of the myelin sheath, causing neurological issues, and adrenal insufficiency.

2025 ICD-10-CM code E61.0

Copper deficiency, a condition characterized by inadequate levels of copper in the body.

2025 ICD-10-CM code E71.121

Propionic acidemia.

2025 ICD-10-CM code E10.36

Type 1 diabetes mellitus with diabetic cataract.

2025 ICD-10-CM code E87.29

Other acidosis. Respiratory acidosis NOS.

2025 ICD-10-CM code E23.0

Hypopituitarism is a condition characterized by the pituitary gland's decreased or absent production of one or more of its hormones.

2025 ICD-10-CM code E09.3419

Drug or chemical-induced diabetes mellitus with severe nonproliferative diabetic retinopathy with macular edema, unspecified eye.

2025 ICD-10-CM code E51.9

Thiamine deficiency, unspecified.

2025 ICD-10-CM code E63.8

Other specified nutritional deficiencies. This code is used when a provider documents a deficiency of a specific nutrient not represented by another code.

2025 ICD-10-CM code E08.3591

Diabetes mellitus due to an underlying condition with proliferative diabetic retinopathy without macular edema, right eye.

2025 ICD-10-CM code E08.3553

Diabetes mellitus due to an underlying condition with stable proliferative diabetic retinopathy affecting both eyes.

2025 ICD-10-CM code E66

Overweight and obesity. Code first obesity complicating pregnancy, childbirth and the puerperium, if applicable (O99.21-). Use additional code to identify body mass index (BMI), if known (Z68.-)

2025 ICD-10-CM code E04.2

Nontoxic multinodular goiter is an enlargement of the thyroid gland with multiple nodules.

2025 ICD-10-CM code E71.529

This code represents an unspecified type of X-linked adrenoleukodystrophy, a genetic disorder affecting the nervous system and adrenal glands.

2025 ICD-10-CM code E07.0

Hypersecretion of calcitonin.

2025 ICD-10-CM code E75.21

Fabry disease (also known as Fabry-Anderson disease) is an inherited disorder characterized by the accumulation of a fatty substance called globotriaosylceramide in the body's cells.

2025 ICD-10-CM code E10.29

Type 1 diabetes mellitus with other specified diabetic kidney complications, such as renal tubular degeneration.