E71.51
Non-billableDisorders of peroxisome biogenesis
Disorders of peroxisome biogenesis
This is a header/category code. For billing purposes, use a more specific child code from the list below.
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Group 1 peroxisomal disorders
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- transitory endocrine and metabolic disorders specific to newborn (P70-P74)
- androgen insensitivity syndrome (E34.5-)
- congenital adrenal hyperplasia (E25.0)
- hemolytic anemias attributable to enzyme disorders (D55.-)
- Marfan syndrome (Q87.4-)
- 5-alpha-reductase deficiency (E29.1)
- Schilder's disease (G37.0)
- Refsum's disease (G60.1)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Child Codes (3)
Also Known As / Clinical Terms
Frequently Asked Questions
What is the ICD-10 code for disorders of peroxisome biogenesis?
The ICD-10-CM code for disorders of peroxisome biogenesis is E71.51. The full clinical description is "Disorders of peroxisome biogenesis". E71.51 is a non-billable header code. Use a more specific child code for billing purposes.
What does ICD-10 code E71.51 mean?
ICD-10-CM code E71.51 represents "Disorders of peroxisome biogenesis". 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.
Is E71.51 a billable code?
No, E71.51 is a non-billable header code. You need to use one of its more specific child codes for billing. There are 3 child codes under E71.51.
What chapter is E71.51 in?
E71.51 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E71.51?
E71.51 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 are the subcategories under E71.51?
E71.51 has 3 child codes, including: E71.510 (Zellweger syndrome), E71.511 (Neonatal adrenoleukodystrophy), E71.518 (Other disorders of peroxisome biogenesis).
What are the UMLS CUIs for E71.51?
E71.51 is linked to 2 UMLS Concept Unique Identifiers: C1832200, C2874247. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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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.