2026 ICD-10-CM Diagnosis Code E71.540Rhizomelic chondrodysplasia punctata
ICD-10-CM Codes›E00–E89›E70-E88›E71
- Billable — Valid for Submission
- Chronic Condition
E71.540 is a billable ICD-10-CM diagnosis code for rhizomelic chondrodysplasia punctata. It is valid on HIPAA claims for fiscal year 2026 (October 1, 2025 through September 30, 2026). Coders also document this condition as loss of multiple peroxisomal functions. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Other specified and unspecified nutritional and metabolic disorders.
Code Identity
Code Classification
Approximate SynonymsGuidance
Alternate terms and clinical phrases that map to this code.
- Loss of multiple peroxisomal functions
- Rhizomelic chondrodysplasia punctata syndrome
- Rhizomelic chondrodysplasia punctata type 1
- Rhizomelic chondrodysplasia punctata type 2
- Rhizomelic chondrodysplasia punctata type 3
Index to Diseases and InjuriesGuidance
Alphabetical index entries that point to this code.
- Disorder (of) - See Also: Disease;
- peroxisomal - E71.50
- rhizomelic chondrodysplasia punctata - E71.540
- Rhizomelic chondrodysplasia punctata - E71.540
External Cause of Injuries IndexGuidance
References for this code in the External Cause of Injuries Index.
- Disorder(of)
- peroxisomal
- rhizomelic chondrodysplasia punctata
- Rhizomelic chondrodysplasia punctata
Clinical ClassificationClinical
AHRQ’s CCSR groups this code into broader clinical categories.
Clinical InformationClinical
Peroxisomal Disorders
a heterogeneous group of inherited metabolic disorders marked by absent or dysfunctional peroxisomes. peroxisomal enzymatic abnormalities may be single or multiple. biosynthetic peroxisomal pathways are compromised, including the ability to synthesize ether lipids and to oxidize long-chain fatty acid precursors. diseases in this category include zellweger syndrome; infantile refsum disease; rhizomelic chondrodysplasia (chondrodysplasia punctata, rhizomelic); hyperpipecolic acidemia; neonatal adrenoleukodystrophy; and adrenoleukodystrophy (x-linked). neurologic dysfunction is a prominent feature of most peroxisomal disorders.
Patient EducationClinical
Metabolic Disorders
Metabolism is the process your body uses to get or make energy from the food you eat. Food is made up of proteins, carbohydrates, and fats. Chemicals in your digestive system break the food parts down into sugars and acids, your body's fuel.
Read the full article at MedlinePlus
Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.
Convert E71.540 to ICD-9-CMHistory
The closest ICD-9-CM equivalents under the General Equivalence Mappings.
Code HistoryHistory
Questions About E71.540Overview
Is E71.540 (Other peroxisomal disorders) a billable code?
Yes. This is a billable ICD-10-CM code, specific enough to report rhizomelic chondrodysplasia punctata on HIPAA-covered claims from October 1, 2025 through September 30, 2026.
What is the ICD-9 equivalent of E71.540?
Under the General Equivalence Mappings, rhizomelic chondrodysplasia punctata converts to ICD-9-CM 277.86 (peroxisomal disorders). The mapping is approximate, so confirm the match fits the documentation.
Footnotes
[1] Chronic - a chronic condition code indicates a condition lasting 12 months or longer and its effect on the patient based on one or both of the following criteria:
- The condition results in the need for ongoing intervention with medical products,treatment, services, and special equipment
- The condition places limitations on self-care, independent living, and social interactions.
