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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 E75.29

This code represents a diagnosis of other sphingolipidosis, encompassing conditions not specifically classified elsewhere within the sphingolipidoses.

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 E74.01

Von Gierke disease (also known as Type I glycogen storage disease). It's a genetic disorder where the body can't break down glycogen, leading to its accumulation and low blood sugar.

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 E71.12

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 E78.41

Elevated lipoprotein(a), also known as Lp(a). This is an inherited condition causing high levels of a cholesterol, fat, and protein-carrying particle in the blood, increasing the risk of coronary artery disease.

2025 ICD-10-CM code E71

Disorders of branched-chain amino-acid metabolism and fatty-acid 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 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 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 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 E78.00

Pure hypercholesterolemia, unspecified. This is a condition characterized by elevated cholesterol levels without a specified cause.

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 E72.01

Cystinuria is a rare, inherited disorder characterized by impaired renal reabsorption of cystine, leading to the formation of cystine stones in the kidneys, ureters, and bladder.

2025 ICD-10-CM code E71.30

Disorder of fatty-acid metabolism, unspecified.

2025 ICD-10-CM code E75.01

Sandhoff disease is a rare, inherited lysosomal storage disorder causing progressive destruction of nerve cells in the brain and spinal cord.

2025 ICD-10-CM code E70.81

Aromatic L-amino acid decarboxylase deficiency (AADC deficiency).

2025 ICD-10-CM code E71.311

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

2025 ICD-10-CM code E85.82

Wild-type transthyretin-related (ATTR) amyloidosis, also known as senile systemic amyloidosis (SSA).

2025 ICD-10-CM code E78.41

Erhöhtes Lipoprotein (a), auch bekannt als Lp (a). Dies ist eine Erbkrankheit, die zu einem hohen Gehalt an Cholesterin-, Fett- und Proteinpartikeln im Blut führt, was das Risiko einer koronaren Herzkrankheit erhöht.

2025 ICD-10-CM code E74.3

Other disorders of intestinal carbohydrate absorption

2025 ICD-10-CM code E75.1

Other and unspecified gangliosidosis. This code is used for gangliosidoses other than GM2 gangliosidosis, or when the specific type of non-GM2 gangliosidosis is not specified.

2025 ICD-10-CM code E70.331

Hermansky-Pudlak syndrome