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ICD-10-CM Code E71.51
Disorders of peroxisome biogenesis

NON-BILLABLE
Non-Billable Code
Non-Billable means the code is not sufficient justification for admission to an acute care hospital when used a principal diagnosis. Use a child code to capture more detail.
| ICD-10 from 2011 - 2016

ICD Code E71.51 is a non-billable code. To code a diagnosis of this type, you must use one of the three child codes of E71.51 that describes the diagnosis 'disorders of peroxisome biogenesis' in more detail.


The ICD code E71 is used to code Congenital disorders of amino acid metabolism

Inborn errors of amino acid metabolism are metabolic disorders which impair the synthesis and degradation of amino acids.

Specialty: Endocrinology
MeSH Code: D000592
ICD 9 Code: 270

The general structure of an α-amino acid, with the amino group on the left and the carboxyl group on the right.

Source: Wikipedia

Coding Notes for E71.51 Info for medical coders on how to properly use this ICD-10 code

Inclusion Terms:
Inclusion Terms
Inclusion Terms are a list of concepts for which a specific code is used. The list of Inclusion Terms is useful for determining the correct code in some cases, but the list is not necessarily exhaustive.
Group 1 peroxisomal disorders
Code Type-1 Excludes:
Type-1 Excludes
Type-1 Excludes mean the conditions excluded are mutually exclusive and should never be coded together. Excludes 1 means "do not code here."
Refsum's disease - instead, use code G60.1

ICD-10-CM Alphabetical Index References for 'E71.51 - Disorders of peroxisome biogenesis'

The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code E71.51. Click on any term below to browse the alphabetical index.


Parent Code: E71.5 - Peroxisomal disorders

** This Document Provided By ICD.Codes **
Source: http://icd.codes/icd10cm/E7151