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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.
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
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