iFrame.AI – Discover What Matters

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 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

2025 ICD-10-CM code E70.32

Oculocutaneous albinism (OCA)

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 E74.04

McArdle disease (also known as type 5 glycogen storage disease or GSD5) is a rare genetic disorder affecting carbohydrate metabolism. It is characterized by a deficiency of the enzyme glycogen phosphorylase, leading to glycogen accumulation in muscle cells.

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 E80.7

Disorder of bilirubin metabolism, unspecified.

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 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 E71.318

Other disorders of fatty-acid oxidation.

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 E87.3

Alkalosis

2025 ICD-10-CM code E86.1

Hypovolemia, or depletion of plasma volume.

2025 ICD-10-CM code E72.89

Other specified disorders of amino-acid metabolism. This encompasses conditions not specifically classified elsewhere, involving disruptions in amino acid processes like synthesis, transport, or breakdown.

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 E70.41

Histidinemia

2025 ICD-10-CM code E80.21

Talamak na paulit-ulit (hepatikong) porphyria. Ito ay isang bihirang minana na karamdaman na nagdudulot ng kakulangan ng porphobilinogen deaminase (<a href="../medical-coding/reference/PBGD" target="_blank" title="Medical Code PBGD 2025">PBGD</a>), na humahantong sa sakit sa tiyan at neurolohikal na sintomas.

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 E72.11

Homocystinuria due to cystathionine synthase deficiency.

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.

Enterprise Edition

Upgrade for detailed insurance, legislation, and other documents analytics for individual cases; real-time analysis of the datasets from your EHR, CRM, ERP, or other software; and more Enterprise Features.