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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 E71.313

Glutaricaciduria type II (GA2)

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 E70.318

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 E74.3

Other disorders of intestinal carbohydrate absorption

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 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 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 E80.7

Disorder of bilirubin metabolism, unspecified.

2025 ICD-10-CM code E85.4

Organ-limited amyloidosis is a condition characterized by the buildup of abnormal amyloid proteins in a single organ.

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 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 E71.50

Peroxisomal disorder, unspecified.

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 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 E78.3

Hyperchylomicronemia, also known as chylomicron retention disease or type I/V Fredrickson hyperlipoproteinemia.It involves elevated chylomicrons and triglycerides.

2025 ICD-10-CM code E71

Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism.

2025 ICD-10-CM code E72.09

Other disorders of amino-acid transport.

2025 ICD-10-CM code E74.8

A disorder affecting carbohydrate metabolism not otherwise specified.

2025 ICD-10-CM code E85.81

Light chain (AL) amyloidosis is a condition characterized by the buildup of abnormal protein fibers, called light chains, in various organs and tissues.

2025 ICD-10-CM code E88.1

Lipodystrophy, not elsewhere classified. This refers to a group of disorders characterized by abnormal distribution or loss of body fat.

2025 ICD-10-CM code E70.9

Disorder of aromatic amino-acid metabolism, unspecified.

2025 ICD-10-CM code E70.40

Disorders of histidine metabolism, unspecified.

2025 ICD-10-CM code E85.2

Heredofamilial amyloidosis, unspecified. This is an inherited disorder characterized by deposits of abnormal amyloid transthyretin (TTR) protein, primarily affecting the liver, nerves, heart, and kidneys.

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 E70.20

Disorder of tyrosine metabolism, unspecified.

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 E79.8

This code refers to inherited metabolic disorders leading to excess uric acid (from purine breakdown) or excess ammonia, carbon dioxide, and beta-amino acids (from pyrimidine breakdown), causing various neurological, hematological, and immunological problems.

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 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).

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