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ALL MEDICAL CODES IN CATEGORY Metabolic disorders

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 E74.81

Disorders of glucose transport, not elsewhere classified.

2025 ICD-10-CM code E72.9

Unspecified disorder of amino-acid metabolism. This code encompasses disorders related to amino acids, the building blocks of proteins, and their role in metabolic processes.

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 E71.111

3-methylglutaconic aciduria (3MGA) is a rare inborn error of metabolism where the body cannot properly process leucine, leading to a buildup of 3-methylglutaconic acid.

2025 ICD-10-CM code E88.49

Other mitochondrial metabolism disorders. This condition affects energy production within cells and impacts organs with high energy needs.

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 E76.9

Unspecified glycosaminoglycan metabolism disorder. This code is used when the specific type of GAG metabolism disorder is not documented.

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 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 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 E72.81

Disorders of gamma-aminobutyric acid (GABA) metabolism. This includes conditions like 4-hydroxybutyric aciduria, GABA transaminase deficiency, and succinic semialdehyde dehydrogenase deficiency.

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 E79.1

Lesch-Nyhan syndrome due to HGPRT deficiency.

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 E74.11

Essential fructosuria is a benign inherited condition characterized by the excess excretion of fructose in the urine due to a deficiency of the enzyme fructokinase.

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 E70.320

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

2025 ICD-10-CM code E87.8

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

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 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 E71.43

Iatrogenic carnitine deficiency is a carnitine deficiency caused by medications.

2025 ICD-10-CM code E72.11

Homocystinuria due to cystathionine synthase deficiency.

2025 ICD-10-CM code E79.2

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

2025 ICD-10-CM code E74.29

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

2025 ICD-10-CM code E70.49

Other disorders of histidine metabolism, encompassing rare inborn errors affecting histidine breakdown.

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 E76.210

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

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 E72.29

This code refers to inherited amino acid disorders, not otherwise specified, affecting the urea cycle, leading to the deficient removal of ammonia from the blood.

2025 ICD-10-CM code E87.79

A type of fluid overload not otherwise specified.

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 E84.0

Cystic fibrosis with pulmonary manifestations.

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

2025 ICD-10-CM code E83.51

Hypocalcemia

2025 ICD-10-CM code E79

Disorders of purine and pyrimidine metabolism.

2025 ICD-10-CM code E74.02

Pompe disease (also known as type 2 glycogen storage disease or acid maltase deficiency) is a rare genetic disorder characterized by the accumulation of glycogen in muscle cells due to a deficiency of the enzyme acid alpha-glucosidase (GAA).

2025 ICD-10-CM code E74.810

Glucose transporter protein type 1 deficiency syndrome (Glut1 DS) is a rare genetic metabolic disorder characterized by impaired glucose transport into the brain.

2025 ICD-10-CM code E71.510

Zellweger syndrome, the most severe form of Zellweger spectrum disorder, is a rare genetic disorder affecting peroxisome function. This leads to the body's inability to metabolize certain fatty acids.

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 E74.819

Disorders of glucose transport, unspecified.

2025 ICD-10-CM code E71.51

Disorder of peroxisome biogenesis, Group 1 peroxisomal disorder. Excludes1: Refsum's disease (G60.1)

2025 ICD-10-CM code E71.548

Other peroxisomal disorders. This code represents a peroxisomal disorder not otherwise specified in the ICD-10-CM.

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 E70.338

A rare inherited disorder characterized by a lack of pigment in the skin, hair, and eyes (albinism) combined with blood clotting abnormalities.

2025 ICD-10-CM code E72.00

Unspecified disorder of amino-acid transport.

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