E71.548
BillableOther peroxisomal disorders
Other peroxisomal disorders
Coding Notes
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Related Codes(3)
Also Known As / Clinical Terms(52)
SNOMED CT
- 3-Ketoacyl-CoA thiolase deficiency238067002
- Peroxisomal thiolase deficiency238067002
- Pseudo-Zellweger syndrome238067002
- Bifunctional peroxisomal enzyme deficiency238068007
- Glutaric acidaemia type 3238070003
- Glutaric acidemia type 3238070003
- Glutaric aciduria type 3238070003
- Glutaryl-CoA oxidase deficiency238070003
- Glutaryl-coenzyme A oxidase deficiency238070003
- SUGCT-gene related glutaryl-coenzyme A oxidase deficiency238070003
- Dihydroxycholestanoic acidaemia and trihydroxycholestanoic acidaemia238071004
- Dihydroxycholestanoic acidemia and trihydroxycholestanoic acidemia238071004
- Trihydroxycholestanoyl-CoA oxidase deficiency238071004
- Isolated DHAP-AT - dihydroxyacetone phosphate acyltransferase deficiency238072006
- Isolated dihydroxyacetone phosphate acyltransferase deficiency238072006
- Isolated alkyldihydroxyacetone phosphate synthase deficiency238073001
- Encephalopathy due to mitochondrial and peroxisomal fission defect1236807002
- FAR1 deficiency1237619001
- Fatty acyl-CoA reductase 1 deficiency1237619001
- Fatty acyl-coenzyme A reductase 1 deficiency1237619001
- PFCRD - peroxisomal fatty acyl-CoA reductase 1 disorder1237619001
- Deficiency of sterol carrier protein X1296861002
- SCPX (sterol carrier protein X) deficiency1296861002
- SCPx (sterol carrier protein x) deficiency1296861002
- Sterol carrier protein X deficiency1296861002
- Sterol carrier protein-2 deficiency1296861002
Clinical Terms
- Deficiency of sterol carrier protein X
- FAR1 deficiency
- Isolated dihydroxyacetone phosphate acyltransferase deficiency
- Pseudo-Zellweger syndrome
- PFCRD - peroxisomal fatty acyl-CoA reductase 1 disorder
- Sterol carrier protein-2 deficiency
- Isolated DHAP-AT - dihydroxyacetone phosphate acyltransferase deficiency
- 3-Ketoacyl-CoA thiolase deficiency
- Dihydroxycholestanoic acidemia and trihydroxycholestanoic acidemia
- Encephalopathy due to mitochondrial and peroxisomal fission defect
- Trihydroxycholestanoyl-CoA oxidase deficiency
- Isolated alkyldihydroxyacetone phosphate synthase deficiency
- Glutaryl-coenzyme A oxidase deficiency
- SCPX (sterol carrier protein X) deficiency
- Glutaric acidaemia type 3
- Glutaric acidemia type 3
- Glutaryl-CoA oxidase deficiency
- Sterol carrier protein X deficiency
- Bifunctional peroxisomal enzyme deficiency
- Fatty acyl-CoA reductase 1 deficiency
- Fatty acyl-coenzyme A reductase 1 deficiency
- SUGCT-gene related glutaryl-coenzyme A oxidase deficiency
- Dihydroxycholestanoic acidaemia and trihydroxycholestanoic acidaemia
- Glutaric aciduria type 3
- Peroxisomal thiolase deficiency
Frequently Asked Questions
What is the ICD-10 code for other peroxisomal disorders?
The ICD-10-CM code for other peroxisomal disorders is E71.548. The full clinical description is "Other peroxisomal disorders". E71.548 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E71.548 mean?
ICD-10-CM code E71.548 represents “Other peroxisomal disorders”. 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 E71.548 a billable code?
Yes, E71.548 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E71.548 in?
E71.548 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E71.548?
E71.548 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.
What SNOMED CT codes does E71.548 map to?
E71.548 maps to 9 SNOMED CT concepts: 238067002, 238068007, 1296861002, 238071004, 1236807002, and 4 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E71.548?
E71.548 is linked to 1 UMLS Concept Unique Identifier: C2874255. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E71.548 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other 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.
What is the ICD-11 equivalent of E71.548?
There is no direct ICD-11 mapping available for E71.548 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.