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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 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 E71.518
Other disorders of peroxisome biogenesis. This condition encompasses inborn errors of metabolism affecting peroxisome function, excluding Zellweger syndrome and neonatal adrenoleukodystrophy.
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 E08.354
Diabetes mellitus due to an underlying condition with proliferative diabetic retinopathy, combined traction and rhegmatogenous retinal detachment.
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 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 E70.30
Albinism, unspecified.This code is used when the specific type of albinism is not documented or unknown.
2025 ICD-10-CM code E74.0
Glycogen storage disease.
2025 ICD-10-CM code E70.330
Chediak-Higashi syndrome
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 E89.820
Postprocedural hematoma of an endocrine system organ or structure following an endocrine system procedure.
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).
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