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ALL MEDICAL CODES IN CATEGORY Chapter 4: Endocrine, Nutritional and Metabolic Diseases (E00-E89)
2025 ICD-10-CM code E24.3
Ectopic ACTH syndrome. This is a rare form of Cushing syndrome caused by the overproduction of adrenocorticotropic hormone (ACTH) by tumors outside the pituitary gland.
2025 ICD-10-CM code E27.49
Other adrenocortical insufficiency. This code is used when the provider documents a type of adrenocortical insufficiency not otherwise classified.
2025 ICD-10-CM code E75.02
Tay-Sachs disease. This is a genetic disorder causing a deficiency of the enzyme beta-hexosaminidase A, leading to the accumulation of GM2 ganglioside in nerve cells.
2025 ICD-10-CM code E80.1
Porphyria cutanea tarda (PCT).
2025 ICD-10-CM code E76.03
Scheie syndrome (MPS I-S) is a rare, inherited metabolic disorder, the mildest form of Mucopolysaccharidosis type I (MPS I), characterized by the accumulation of glycosaminoglycans in the body.
2025 ICD-10-CM code E32.0
Persistent hyperplasia of the thymus.Enlargement of the thymus gland beyond its normal size for age.
2025 ICD-10-CM code E75.26
Sulfatase deficiency, also known as multiple sulfatase deficiency (MSD).
2025 ICD-10-CM code E75.19
This code represents other types of gangliosidosis not specifically identified by other codes, such as GM1 and GM3.
2025 ICD-10-CM code E72.8
This code encompasses disorders of amino-acid metabolism not classified elsewhere. These may involve issues with the synthesis, transport, or breakdown of amino acids.
2025 ICD-10-CM code E50.4
Vitamin A deficiency with keratomalacia.
2025 ICD-10-CM code E74.0
Glycogen storage disease.
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 E50.9
Vitamin A deficiency, unspecified.
2025 ICD-10-CM code E75.22
Gaucher disease, a genetic disorder characterized by the deficiency of beta-glucocerebrosidase, leading to the accumulation of glucocerebroside in various organs.
2025 ICD-10-CM code E89.820
Postprocedural hematoma of an endocrine system organ or structure following an endocrine system procedure.
2025 ICD-10-CM code E71.518
Other disorders of peroxisome biogenesis. This condition encompasses inborn errors of metabolism affecting peroxisome function, excluding Zellweger syndrome and neonatal adrenoleukodystrophy.
Diabetes mellitus due to an underlying condition with proliferative diabetic retinopathy, combined traction and rhegmatogenous retinal detachment.
2025 ICD-10-CM code E70.330
Chediak-Higashi syndrome
2025 ICD-10-CM code E71.51
Disorder of peroxisome biogenesis, Group 1 peroxisomal disorder. Excludes1: Refsum's disease (G60.1)
2025 ICD-10-CM code E26.8
Other hyperaldosteronism.
2025 ICD-10-CM code E53.8
Deficiency of other specified B group vitamins. This includes deficiencies in B vitamins not otherwise classified, such as pantothenic acid (B5), biotin (B7), and other B complex vitamins.
2025 ICD-10-CM code E70.319
Unspecified ocular albinism (OA) is an inherited eye disorder characterized by diminished pigmentation in the iris and retina.It primarily affects males.
2025 ICD-10-CM code E70.30
Albinism, unspecified.This code is used when the specific type of albinism is not documented or unknown.
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