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ALL MEDICAL CODES IN CATEGORY E70-E88 (Metabolic disorders)

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 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 E70.320

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

2025 ICD-10-CM code E71.43

Iatrogenic carnitine deficiency is a carnitine deficiency caused by medications.

2025 ICD-10-CM code E76.1

Mucopolysaccharidosis, type II (Hunter syndrome) is an inherited disorder causing a deficiency of iduronate 2-sulfatase. This leads to the accumulation of glycosaminoglycans in cells, causing multi-systemic dysfunction.

2025 ICD-10-CM code E75.09

Other GM2 gangliosidosis. This includes adult and juvenile GM2 gangliosidosis not otherwise specified.

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 E74.89

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

2025 ICD-10-CM code E70

Disorders of aromatic amino-acid metabolism.

2025 ICD-10-CM code E70.39

Other specified albinism. This includes conditions like Piebaldism where there are symmetrical hypopigmented or depigmented patches of skin and a midline patch of white hair.

2025 ICD-10-CM code E72.51

Non-ketotic hyperglycinemia (NKH), also known as glycine encephalopathy.

2025 ICD-10-CM code E70.319

Unspecified ocular albinism (OA) is an inherited eye disorder characterized by diminished pigmentation in the iris and retina.It primarily affects males.

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 E76.03

Scheie syndrome (MPS I-S) is a rare, inherited metabolic disorder, the mildest form of Mucopolysaccharidosis type I (MPS I), characterized by the accumulation of glycosaminoglycans in the body.

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 E76.21

Morquio mucopolysaccharidoses, also known as mucopolysaccharidosis type IV (MPS IV), is an inherited autosomal recessive disorder primarily affecting the skeleton.

2025 ICD-10-CM code E74.0

Glycogen storage disease.

2025 ICD-10-CM code E72.0

Disorders of amino-acid transport. This condition impacts the body's ability to absorb amino acids, essential building blocks of proteins, from the kidneys and intestines.

2025 ICD-10-CM code E70.331

Hermansky-Pudlak syndrome

2025 ICD-10-CM code E76.01

Hurler syndrome, a severe form of mucopolysaccharidosis type I (MPS I).

2025 ICD-10-CM code E70.339

Unspecified albinism with hematologic abnormality.

2025 ICD-10-CM code E70.5

Disorders of tryptophan metabolism.

2025 ICD-10-CM code E83

Disorders of mineral metabolism

2025 ICD-10-CM code E77

Disorders of glycoprotein metabolism, encompassing inherited conditions affecting the breakdown or transport of complex carbohydrates.

2025 ICD-10-CM code E70.321

Tyrosinase-positive oculocutaneous albinism (OCA2) is a genetic condition causing reduced pigmentation in the skin, hair, and eyes, leading to various vision problems.

2025 ICD-10-CM code E75.4

Neuronal ceroid lipofuscinosis (NCL) is a group of inherited, progressive neurodegenerative disorders characterized by the accumulation of lipofuscins in brain cells, leading to vision loss, seizures, and dementia.It encompasses various subtypes, including Batten disease, Bielschowsky-Jansky disease, and Kufs disease.

2025 ICD-10-CM code E72.59

Other disorders of glycine metabolism. This includes conditions like D-glycericacidemia, hyperhydroxyprolinemia, type I and II hyperprolinemia, and sarcosinemia.

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 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 E71.39

A disorder affecting the body's process of converting fatty acids into energy. This code is used for fatty-acid metabolism disorders not otherwise specified.

2025 ICD-10-CM code E70.330

Chediak-Higashi syndrome

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 E76

Disorders of glycosaminoglycan metabolism. These are inherited lysosomal storage disorders causing enzyme deficiencies that lead to abnormal accumulation of glycosaminoglycans.

2025 ICD-10-CM code E73.9

Lactose intolerance, unspecified. This signifies the inability to digest lactose (milk sugar) due to lactase deficiency, without specifying the type of lactose intolerance.

2025 ICD-10-CM code E74.09

Other glycogen storage disease. This includes conditions like Andersen disease, Hers disease, and Tarui disease, which are caused by enzyme deficiencies affecting glycogen metabolism.

2025 ICD-10-CM code E70.2

Disorders of tyrosine metabolism. This code excludes transitory tyrosinemia of the newborn (P74.5).

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 E76.3

Mucopolysaccharidosis, unspecified. This code is used when the specific type of mucopolysaccharidosis is not documented.

2025 ICD-10-CM code E72.4

Disorders of ornithine metabolism, including hyperammonemia-hyperornithinemia-homocitrullinuria (HHH) syndrome, ornithinemia, and ornithine transcarbamylase deficiency.

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).

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