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ALL MEDICAL CODES IN CATEGORY 4 Endocrine, Nutritional and Metabolic Diseases

2025 ICD-10-CM code E11.40

Type 2 diabetes mellitus with diabetic neuropathy, unspecified.

2025 ICD-10-CM code E09.319

Diabetes due to drugs/chemicals with retinopathy, no macular edema.

2025 ICD-10-CM code E83.49

Other disorders of magnesium metabolism. This code is used for magnesium metabolism disorders not otherwise specified, including conditions related to malabsorption and excretion defects.

2025 ICD-10-CM code E71.120

Methylmalonic acidemia (MMA) is a rare genetic disorder characterized by the body's inability to properly break down certain proteins and fats, leading to a harmful buildup of substances.

2025 ICD-10-CM code E04.9

Unspecified nontoxic goiter. This condition involves an enlarged thyroid gland without disturbances in thyroid function, excluding cases caused by iodine deficiency.

2025 ICD-10-CM code E84.11

Meconium ileus in cystic fibrosis. This is a bowel obstruction in newborns caused by thickened meconium due to cystic fibrosis.

2025 ICD-10-CM code E09.49

Diabetes mellitus due to drugs or chemicals, with neurological complications, and other specified diabetic neurological complication.

2025 ICD-10-CM code E43

Severe protein-calorie malnutrition, unspecified.

2025 ICD-10-CM code E10.51

Type 1 diabetes mellitus with diabetic peripheral angiopathy without gangrene.

2025 ICD-10-CM code E34.52

Partial androgen insensitivity syndrome. This is a genetic disorder where a genetically male individual is partially resistant to male hormones (androgens), leading to female or mixed male/female physical traits.

2025 ICD-10-CM code E71.314

Muscle carnitine palmitoyltransferase deficiency. This is an inherited metabolic disorder where the body cannot properly break down certain fats for energy due to reduced enzyme activity.

2025 ICD-10-CM code E23.2

Diabetes insipidus. A disorder characterized by excretion of large amounts of urine, accompanied by excessive thirst.

2025 ICD-10-CM code E79.2

Myoadenylate deaminase deficiency (MADD), a rare inherited disorder affecting purine metabolism.

2025 ICD-10-CM code E11.339

Type 2 diabetes mellitus with moderate nonproliferative diabetic retinopathy without macular edema.

2025 ICD-10-CM code E11.3522

Type 2 diabetes mellitus with proliferative diabetic retinopathy with traction retinal detachment involving the macula of the left eye.

2025 ICD-10-CM code E08.641

Diabetes mellitus due to an underlying condition complicated by hypoglycemia and coma.

2025 ICD-10-CM code E88.01

Alpha-1 antitrypsin deficiency (AAT deficiency) is a genetic disorder characterized by low levels of alpha-1 antitrypsin (AAT) in the blood and lungs. This deficiency can lead to lung and liver diseases.

2025 ICD-10-CM code E09.3311

Diabetes caused by drugs/chemicals with moderate nonproliferative diabetic retinopathy and macular edema in the right eye.

2025 ICD-10-CM code E10.3519

Type 1 diabetes mellitus with proliferative diabetic retinopathy with macular edema, unspecified eye.

2025 ICD-10-CM code E84.0

Cystic fibrosis with pulmonary manifestations.

2025 ICD-10-CM code E84.8

Cystic fibrosis with other manifestations. This code is used for cases of cystic fibrosis where the manifestations are not primarily respiratory or intestinal.

2025 ICD-10-CM code E83.9

A disorder of mineral metabolism, unspecified.

2025 ICD-10-CM code E45

Retarded development following protein-calorie malnutrition (PCM).

2025 ICD-10-CM code E70.0

Classical phenylketonuria (PKU) is a genetic disorder where the body cannot break down phenylalanine, leading to its buildup.

2025 ICD-10-CM code E74.21

Galactosemia is an inherited disorder affecting galactose metabolism.