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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 E74.3

Other disorders of intestinal carbohydrate absorption

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 E70.32

Oculocutaneous albinism (OCA)

2025 ICD-10-CM code E86.9

Volume depletion, unspecified.

2025 ICD-10-CM code E79

Disorders of purine and pyrimidine metabolism.

2025 ICD-10-CM code E71.11

Branched-chain organic acidurias are a group of inherited metabolic disorders characterized by the body's inability to properly break down certain amino acids, leading to a harmful buildup of organic acids in the blood and urine.

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 E85.89

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

2025 ICD-10-CM code E80.7

Disorder of bilirubin metabolism, unspecified.

2025 ICD-10-CM code E70.329

Oculocutaneous albinism, unspecified. This code is used when the specific type of oculocutaneous albinism (OCA) is not documented.

2025 ICD-10-CM code E78.9

Disorder of lipoprotein metabolism, unspecified.

2025 ICD-10-CM code E71.52

X-linked adrenoleukodystrophy. This is a genetic disorder primarily affecting the nervous system and adrenal glands in males.

2025 ICD-10-CM code E71.1

Other disorders of branched-chain amino-acid metabolism.

2025 ICD-10-CM code E75

Disorders of sphingolipid metabolism and other lipid storage disorders

2025 ICD-10-CM code E72.1

Disorders of sulfur-bearing amino-acid metabolism

2025 ICD-10-CM code E75.02

Tay-Sachs disease. This is a genetic disorder causing a deficiency of the enzyme beta-hexosaminidase A, leading to the accumulation of GM2 ganglioside in nerve cells.

2025 ICD-10-CM code E70.3

Albinism.

2025 ICD-10-CM code E75.242

Niemann-Pick disease, type C.

2025 ICD-10-CM code E71.540

Rhizomelic chondrodysplasia punctata (RCDP).

2025 ICD-10-CM code E86

Volume depletion. Use additional code(s) for any associated disorders of electrolyte and acid-base balance (E87.-).

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 E78.89

This code represents other lipoprotein metabolism disorders, encompassing conditions not specifically classified elsewhere.

2025 ICD-10-CM code E71.110

Isovaleric acidemia, a rare genetic disorder characterized by the body's inability to break down the amino acid leucine.

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 E76.02

Hurler-Scheie syndrome (MPS IH/S) is an inherited disorder where the body cannot break down certain complex sugars.

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 E71.3

Disorders of fatty-acid metabolism.

2025 ICD-10-CM code E70.20

Disorder of tyrosine metabolism, unspecified.

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 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 E75.0

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

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 E71.5

Peroxisomal disorders.

2025 ICD-10-CM code E73.8

Other lactose intolerance. This code is used when the provider documents a type of lactose intolerance not otherwise specified, such as primary lactose intolerance.

2025 ICD-10-CM code E78.0

Pure hypercholesterolemia. This is a genetic disorder causing high cholesterol levels, specifically high low-density lipoprotein (LDL) cholesterol, unrelated to diet or lifestyle.

2025 ICD-10-CM code E72.3

Disorders of lysine and hydroxylysine metabolism, encompassing conditions like glutaric aciduria type I, hydroxylysinemia, and hyperlysinemia.

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.