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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 E28.319

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

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 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 E56

A deficiency in vitamins other than those specifically classified elsewhere.

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 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 E83.19

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

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 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 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 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 E01.8

Other iodine-deficiency related thyroid disorders and allied conditions. This code is used for conditions not otherwise specified in the iodine-deficiency related thyroid disorder category.

2025 ICD-10-CM code E56.9

Unspecified vitamin deficiency. This code is used when the provider doesn't specify which vitamin is deficient.

2025 ICD-10-CM code E75.242

Niemann-Pick disease, type C.

2025 ICD-10-CM code E11.9

Type 2 diabetes mellitus without complications.

2025 ICD-10-CM code E71.540

Rhizomelic chondrodysplasia punctata (RCDP).

2025 ICD-10-CM code E85.3

Secondary systemic amyloidosis. This condition involves the buildup of abnormal proteins in various organs and tissues due to an underlying chronic inflammatory disease or long-term dialysis.

2025 ICD-10-CM code E08.352

Diabetes mellitus due to an underlying condition with proliferative diabetic retinopathy and traction retinal detachment involving the macula.

2025 ICD-10-CM code E88.9

A metabolic disorder is a condition that affects the chemical processes involved in converting food into energy at the cellular level.This code signifies an unspecified metabolic disorder, where the specific type is not documented.

2025 ICD-10-CM code E75.23

Krabbe disease (globoid cell leukodystrophy) is a rare, inherited disorder affecting the nervous system. It is caused by a deficiency of the enzyme galactosylceramidase.

2025 ICD-10-CM code E75.25

Metachromatic leukodystrophy (MLD) is a rare, inherited disorder characterized by the deficiency of arylsulfatase A, leading to sulfatide accumulation and progressive damage to the nervous system.

2025 ICD-10-CM code E71.41

Primary carnitine deficiency, a genetic disorder characterized by the body's inability to metabolize fatty acids due to a carnitine deficiency or a defect in its cellular transport.

2025 ICD-10-CM code E78.70

Disorder of bile acid and cholesterol metabolism, unspecified.

2025 ICD-10-CM code E74.89

Other specified disorders of carbohydrate metabolism. This includes conditions like essential pentosuria.

2025 ICD-10-CM code E50.7

Other ocular manifestations of vitamin A deficiency. This code is used when the ocular manifestation is not represented by another code, such as xerophthalmia.

2025 ICD-10-CM code E75.5

Other lipid storage disorders including cerebrotendinous cholesterosis (van Bogaert-Scherer-Epstein disease) and Wolman disease.

2025 ICD-10-CM code E78.49

Other hyperlipidemia. This code is used when the specific type of hyperlipidemia is not otherwise specified in the ICD-10-CM.

2025 ICD-10-CM code E70.21

Tyrosinemia, also known as hypertyrosinemia, is a condition characterized by elevated levels of the amino acid tyrosine in the blood.

2025 ICD-10-CM code E70.328

Other oculocutaneous albinism (OCA) is an inherited condition causing a lack of pigment in skin, hair, and eyes. This code specifies OCA types other than 1 and 2.

2025 ICD-10-CM code E74.12

Hereditary fructose intolerance (HFI) is an inherited disorder characterized by the body's inability to process fructose properly.

2025 ICD-10-CM code E41

Nutritional marasmus. Severe malnutrition characterized by energy deficiency.

2025 ICD-10-CM code E34.329

Unspecified genetic causes of short stature.

2025 ICD-10-CM code E85.1

Neuropathic heredofamilial amyloidosis. A condition characterized by the buildup of amyloid proteins in the peripheral and autonomic nerves due to mutations in the transthyretin (TTR) gene.

2025 ICD-10-CM code E74.03

Cori disease, also known as Forbes disease or type III glycogen storage disease, is an inherited disorder of carbohydrate metabolism.

2025 ICD-10-CM code E72.19

Other disorders of sulfur-bearing amino-acid metabolism. This includes conditions not otherwise specified, such as cystathioninuria, methioninemia, and sulfite oxidase deficiency.

2025 ICD-10-CM code E84.9

Cystic fibrosis, unspecified. This code is used when the provider does not document the specific type of CF or any specific manifestations.

2025 ICD-10-CM code E77.1

Defects in glycoprotein degradation, encompassing conditions like Aspartylglucosaminuria, Fucosidosis, Mannosidosis, and Sialidosis (mucolipidosis I).

2025 ICD-10-CM code E89.821

Postprocedural hematoma of an endocrine system organ or structure following a non-endocrine procedure.

2025 ICD-10-CM code E71.0

Maple syrup urine disease (MSUD) is a rare, inherited metabolic disorder characterized by the body's inability to break down certain amino acids (leucine, isoleucine, and valine). This leads to a buildup of these amino acids and their byproducts in the body, causing various symptoms.

2025 ICD-10-CM code E74.00

Glycogen storage disease, unspecified.

2025 ICD-10-CM code E76.8

Other disorders of glycosaminoglycan metabolism. This code is used for GAG metabolism disorders not otherwise specified in the ICD-10-CM.

2025 ICD-10-CM code E88.0

Disorders of plasma-protein metabolism, not elsewhere classified.