E71.548
BillableOther peroxisomal disorders
Other peroxisomal disorders
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
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
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
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.
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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.