E71.518
BillableOther disorders of peroxisome biogenesis
Other disorders of peroxisome biogenesis
Coding Notes
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-)
Also Known As / Clinical Terms
SNOMED CT
- BASD - Bile acid synthetic defect235915002
- Bile acid synthesis disorder235915002
- Bile acid synthetic defect235915002
- Disorder of bile acid synthesis235915002
- Inborn error of bile acid synthesis235915002
- Synthetic defect of bile acids235915002
- General loss of peroxisomal function238060000
- AMACR deficiency700463002
- Alpha-methylacyl-CoA racemase deficiency disorder700463002
- Congenital bile acid synthesis defect type 4700463002
- PBD-ZSS - Peroxisome biogenesis disorder Zellweger syndrome spectrum742876007
- Peroxisome biogenesis disorder742876007
- Peroxisome biogenesis disorder spectrum742876007
- PEX26 deficiency1187522009
- Peroxisome biogenesis disorder due to PEX26 mutation1187522009
- PEX3 deficiency1187523004
- Peroxisome biogenesis disorder due to PEX3 mutation1187523004
- PEX19 deficiency1187524005
- Peroxisome biogenesis disorder due to PEX19 mutation1187524005
- PEX2 deficiency1187525006
- Peroxisome biogenesis disorder due to PEX2 mutation1187525006
- PEX16 deficiency1187526007
- Peroxisome biogenesis disorder due to PEX16 mutation1187526007
- PEX13 deficiency1187527003
- Peroxisome biogenesis disorder due to PEX13 mutation1187527003
- PEX14 deficiency1187528008
- Peroxisome biogenesis disorder due to PEX14 mutation1187528008
- PEX10 deficiency1187529000
- Peroxisome biogenesis disorder due to PEX10 mutation1187529000
- PEX12 deficiency1187530005
- Peroxisome biogenesis disorder due to PEX12 mutation1187530005
- PEX1 deficiency1187532002
- Peroxisome biogenesis disorder due to PEX1 mutation1187532002
- PEX5 deficiency1187548001
- Peroxisome biogenesis disorder due to PEX5 mutation1187548001
- PEX6 deficiency1187550009
- Peroxisome biogenesis disorder due to PEX6 mutation1187550009
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.
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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.