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ALL MEDICAL CODES IN CATEGORY Metabolic disorders (E70-E88)
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 E75.00
Unspecified GM2 gangliosidosis. This is a group of inherited lipid storage disorders caused by beta-hexosaminidase deficiency.
2025 ICD-10-CM code E74
Other disorders of carbohydrate metabolism
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 E78.2
Mixed hyperlipidemia. This condition involves elevated levels of both cholesterol and triglycerides in the blood.
2025 ICD-10-CM code E78
Disorders of lipoprotein metabolism and other lipidemias.
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 E72
Other disorders of amino-acid metabolism, excluding specified amino acid disorders.
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 E71.313
Glutaricaciduria type II (GA2)
2025 ICD-10-CM code E70.318
Other ocular albinism refers to reduced pigmentation in the iris and retina, excluding X-linked or autosomal recessive forms.
2025 ICD-10-CM code E71.40
Unspecified disorder of carnitine metabolism.
2025 ICD-10-CM code E72.11
Homocystinuria due to cystathionine synthase deficiency.
2025 ICD-10-CM code E74.29
Other disorders of galactose metabolism. This includes conditions such as galactokinase deficiency.
2025 ICD-10-CM code E75.240
Niemann-Pick disease type A. Acid sphingomyelinase deficiency type A (ASMD type A). Infantile neurovisceral acid sphingomyelinase deficiency.
2025 ICD-10-CM code E85
Amyloidosis
2025 ICD-10-CM code E74.0
Glycogen storage disease.
2025 ICD-10-CM code E76.210
Morquio A mucopolysaccharidoses. This is an inherited disorder primarily affecting the skeleton.
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 E83.42
Hypomagnesemia, a condition characterized by low magnesium levels in the blood.
2025 ICD-10-CM code E86.0
Dehydration
2025 ICD-10-CM code E70.330
Chediak-Higashi syndrome
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 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 E71.31
Disorder of fatty-acid oxidation.
2025 ICD-10-CM code E88.2
Lipomatosis, not elsewhere classified. This condition is characterized by the presence of multiple benign fatty deposits (lipomas) throughout the body.
2025 ICD-10-CM code E73.0
Congenital lactase deficiency.
2025 ICD-10-CM code E79.0
Hyperuricemia without signs of inflammatory arthritis and tophaceous disease.A metabolic disorder with excess uric acid in the blood but without kidney stones, joint inflammation, or tophi.
2025 ICD-10-CM code E71.50
Peroxisomal disorder, unspecified.
2025 ICD-10-CM code E78.4
A type of hyperlipidemia not classified elsewhere.
2025 ICD-10-CM code E88.8
Other specified metabolic disorders.
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 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 E71.310
Long-chain/very long chain acyl-CoA dehydrogenase deficiency. This metabolic disorder impairs the body's ability to break down certain fats for energy.
2025 ICD-10-CM code E80.21
Acute intermittent (hepatic) porphyria. This is a rare inherited disorder causing deficiency of porphobilinogen deaminase (PBGD), leading to abdominal pain and neurological symptoms.
2025 ICD-10-CM code E77.9
Unspecified disorder of glycoprotein metabolism.
2025 ICD-10-CM code E75.26
Sulfatase deficiency, also known as multiple sulfatase deficiency (MSD).
2025 ICD-10-CM code E70.33
A rare, inherited disorder characterized by a lack of pigment in the skin, hair, and eyes, accompanied by prolonged bleeding times.
2025 ICD-10-CM code E73.1
Secondary lactase deficiency, an acquired condition where the body doesn't produce enough lactase, the enzyme needed to digest lactose (milk sugar).
2025 ICD-10-CM code E70.30
Albinism, unspecified.This code is used when the specific type of albinism is not documented or unknown.
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 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 E84.1
Cystic fibrosis with intestinal manifestations.
2025 ICD-10-CM code E76.211
Morquio B mucopolysaccharidoses is a rare, inherited metabolic disorder primarily affecting the skeleton. It's characterized by a deficiency of the enzyme beta-galactosidase, leading to an accumulation of keratan sulfate.
2025 ICD-10-CM code E76.29
This code encompasses mucopolysaccharidoses (MPS) not otherwise specified, including Maroteaux-Lamy syndrome (MPS VI) and MPS VII (Sly syndrome).
2025 ICD-10-CM code E72.03
Lowe syndrome. Use additional code for associated glaucoma (H42)
2025 ICD-10-CM code E72.23
Citrullinemia is a rare inherited disorder affecting the urea cycle, leading to ammonia buildup in the blood.
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