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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 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.
2025 ICD-10-CM code E75.240
Niemann-Pick disease type A. Acid sphingomyelinase deficiency type A (ASMD type A). Infantile neurovisceral acid sphingomyelinase deficiency.
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 E71.42
Carnitine deficiency due to inborn errors of metabolism. This is a genetic disorder characterized by the body's inability to process fatty acids due to insufficient carnitine or issues with its cellular transport.
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 E70.330
Chediak-Higashi syndrome
2025 ICD-10-CM code E70.31
Ocular albinism. This condition primarily affects the eyes, reducing pigmentation in the iris and retina.
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 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 E71.31
Disorder of fatty-acid oxidation.
2025 ICD-10-CM code E88.2
Lipomatosis, not elsewhere classified. This condition is characterized by the presence of multiple benign fatty deposits (lipomas) throughout the body.
2025 ICD-10-CM code E73.0
Congenital lactase deficiency.
2025 ICD-10-CM code E79.0
Hyperuricemia without signs of inflammatory arthritis and tophaceous disease.A metabolic disorder with excess uric acid in the blood but without kidney stones, joint inflammation, or tophi.
2025 ICD-10-CM code E71.50
Peroxisomal disorder, unspecified.
2025 ICD-10-CM code E78.4
A type of hyperlipidemia not classified elsewhere.
2025 ICD-10-CM code E88.8
Other specified metabolic disorders.
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 E72.09
Other disorders of amino-acid transport.
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 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 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 E87.70
Fluid overload, unspecified.
2025 ICD-10-CM code E70.9
Disorder of aromatic amino-acid metabolism, unspecified.
2025 ICD-10-CM code E88
Other and unspecified metabolic disorders
2025 ICD-10-CM code E70.40
Disorders of histidine metabolism, unspecified.
2025 ICD-10-CM code E88.3
Tumor lysis syndrome
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 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 E87.3
Alkalosis
2025 ICD-10-CM code E86.1
Hypovolemia, or depletion of plasma volume.
2025 ICD-10-CM code E76.22
Sanfilippo mucopolysaccharidosis, also known as mucopolysaccharidosis type III (MPS III).
2025 ICD-10-CM code E78.8
A disorder characterized by the body's inability to process lipoproteins effectively, leading to abnormal levels of fats in the blood.
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