AutoICD API

E71.518

Billable

Other disorders of peroxisome biogenesis

Other disorders of peroxisome biogenesis

Status

Billable / Specific

Block

E70-E88

Parent Code

E71.51

Coding Notes

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

Excludes 2

Conditions not included here, but the patient may have both

Related Codes(2)
E71.510

Zellweger syndrome

BillableE71.511

Neonatal adrenoleukodystrophy

Billable
Also Known As / Clinical Terms(75)

SNOMED CT

UMLS

Clinical Terms

  • PEX5 deficiency
  • Peroxisome biogenesis disorder due to PEX19 mutation
  • Peroxisome biogenesis disorder due to PEX5 mutation
  • Peroxisome biogenesis disorder due to PEX3 mutation
  • Peroxisome biogenesis disorder spectrum
  • PEX1 deficiency
  • PEX2 deficiency
  • Peroxisome biogenesis disorder
  • Peroxisome biogenesis disorder due to PEX10 mutation
  • PEX10 deficiency
  • Congenital bile acid synthesis defect type 4
  • Disorder of bile acid synthesis
  • Bile acid synthesis disorder
  • PEX26 deficiency
  • PEX13 deficiency
  • PEX12 deficiency
  • Peroxisome biogenesis disorder due to PEX26 mutation
  • Bile acid synthetic defect
  • Peroxisome biogenesis disorder due to PEX13 mutation
  • AMACR deficiency
  • Peroxisome biogenesis disorder due to PEX14 mutation
  • PEX3 deficiency
  • Inborn error of bile acid synthesis
  • BASD - Bile acid synthetic defect
  • PEX14 deficiency
  • PEX16 deficiency
  • Peroxisome biogenesis disorder due to PEX6 mutation
  • Synthetic defect of bile acids
  • Peroxisome biogenesis disorder due to PEX1 mutation
  • Alpha-methylacyl-CoA racemase deficiency disorder
  • General loss of peroxisomal function
  • Peroxisome biogenesis disorder due to PEX16 mutation
  • PBD-ZSS - Peroxisome biogenesis disorder Zellweger syndrome spectrum
  • PEX19 deficiency
  • Peroxisome biogenesis disorder due to PEX2 mutation
  • PEX6 deficiency
  • Peroxisome biogenesis disorder due to PEX12 mutation
Frequently Asked Questions
What is the ICD-10 code for other disorders of peroxisome biogenesis?

The ICD-10-CM code for other disorders of peroxisome biogenesis is E71.518. The full clinical description is "Other disorders of peroxisome biogenesis". E71.518 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code E71.518 mean?

ICD-10-CM code E71.518 represents “Other disorders of peroxisome biogenesis”. It is classified under Chapter 4: Endocrine, Nutritional and Metabolic Diseases and is a billable/specific code that can be used on a claim.

Is E71.518 a billable code?

Yes, E71.518 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is E71.518 in?

E71.518 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).

What codes cannot be used with E71.518?

E71.518 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 5 more.

What SNOMED CT codes does E71.518 map to?

E71.518 maps to 16 SNOMED CT concepts: 700463002, 235915002, 238060000, 742876007, 1187532002, and 11 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for E71.518?

E71.518 is linked to 1 UMLS Concept Unique Identifier: C2874248. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does E71.518 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other disorders of peroxisome biogenesis 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.

What is the ICD-11 equivalent of E71.518?

There is no direct ICD-11 mapping available for E71.518 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.

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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.