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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 E74.0
Glycogen storage disease.
2025 ICD-10-CM code E70.330
Chediak-Higashi syndrome
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 E70.339
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 E75.09
Other GM2 gangliosidosis. This includes adult and juvenile GM2 gangliosidosis not otherwise specified.
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 E75.25
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 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 E70.21
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 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 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 E71.0
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 E76.29
This code encompasses mucopolysaccharidoses (MPS) not otherwise specified, including Maroteaux-Lamy syndrome (MPS VI) and MPS VII (Sly syndrome).
2025 ICD-10-CM code E76.01
Hurler syndrome, a severe form of mucopolysaccharidosis type I (MPS I).
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 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 E70.2
Disorders of tyrosine metabolism. This code excludes transitory tyrosinemia of the newborn (P74.5).
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 E72.51
Non-ketotic hyperglycinemia (NKH), also known as glycine encephalopathy.
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 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 E76.3
Mucopolysaccharidosis, unspecified. This code is used when the specific type of mucopolysaccharidosis is not documented.
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 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 E71.43
Iatrogenic carnitine deficiency is a carnitine deficiency caused by medications.
2025 ICD-10-CM code E70.331
Hermansky-Pudlak 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 E70.39
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 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 E72.4
Disorders of ornithine metabolism, including hyperammonemia-hyperornithinemia-homocitrullinuria (HHH) syndrome, ornithinemia, and ornithine transcarbamylase deficiency.
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