E71.5

The ICD-10-CM code for peroxisomal disorders is E71.5. The full clinical description is "Peroxisomal disorders". E71.5 is a non-billable header code. Use a more specific child code for billing purposes.

ICD-10-CM code E71.5 represents “Peroxisomal disorders”. It is classified under Chapter 4: Endocrine, Nutritional and Metabolic Diseases and is a non-billable header code. Use a more specific child code for billing purposes.

No, E71.5 is a non-billable header code. You need to use one of its more specific child codes for billing. There are 5 child codes under E71.5.

E71.5 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).

E71.5 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); and 4 more.

E71.5 has 5 child codes, including: E71.50 (Peroxisomal disorder, unspecified), E71.51 (Disorders of peroxisome biogenesis), E71.52 (X-linked adrenoleukodystrophy), E71.53 (Other group 2 peroxisomal disorders), and 1 more.

E71.5 is linked to 1 UMLS Concept Unique Identifier: C0282528. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like peroxisomal disorders affect a person's functioning: body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

There is no direct ICD-11 mapping available for E71.5 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.