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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 E72.11

Homocystinuria due to cystathionine synthase deficiency.

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 E85.89

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

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 E74.39

Inability of the small intestines to break down and absorb carbohydrates.

2025 ICD-10-CM code E70.29

This code refers to other disorders of tyrosine metabolism, including alkaptonuria and ochronosis. It excludes transitory tyrosinemia of the newborn.

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 E71.12

A disorder of propionate metabolism characterized by the body's inability to properly process propionic acid, leading to its accumulation.

2025 ICD-10-CM code E71.50

Peroxisomal disorder, unspecified.

2025 ICD-10-CM code E88.8

Other specified metabolic disorders.

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 E72.09

Other disorders of amino-acid transport.

2025 ICD-10-CM code E76.2

Other mucopolysaccharidoses are a group of inherited disorders where the body cannot break down certain complex sugar molecules, leading to their accumulation in tissues and organs.

2025 ICD-10-CM code E88

Other and unspecified metabolic disorders

2025 ICD-10-CM code E77.8

A group of inherited metabolic disorders caused by deficiency or inactivation of proteins/enzymes involved in the breakdown or transport of complex carbohydrates.

2025 ICD-10-CM code E71.310

Long-chain/very long chain acyl-CoA dehydrogenase deficiency. This metabolic disorder impairs the body's ability to break down certain fats for energy.

2025 ICD-10-CM code E80.21

Acute intermittent (hepatic) porphyria. This is a rare inherited disorder causing deficiency of porphobilinogen deaminase (PBGD), leading to abdominal pain and neurological symptoms.

2025 ICD-10-CM code E73.1

Secondary lactase deficiency, an acquired condition where the body doesn't produce enough lactase, the enzyme needed to digest lactose (milk sugar).

2025 ICD-10-CM code E70.30

Albinism, unspecified.This code is used when the specific type of albinism is not documented or unknown.

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 E84.1

Cystic fibrosis with intestinal manifestations.

2025 ICD-10-CM code E87.22

Chronic metabolic acidosis.

2025 ICD-10-CM code E80

Disorders of porphyrin and bilirubin metabolism. Includes defects of catalase and peroxidase.

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 E77.0

Defects in post-translational modification of lysosomal enzymes. Includes Mucolipidosis II (I-cell disease) and Mucolipidosis III (pseudo-Hurler polydystrophy).

2025 ICD-10-CM code E71.30

Disorder of fatty-acid metabolism, unspecified.

2025 ICD-10-CM code E71.311

Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency.

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 E74.29

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

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