Valid for Submission
G71.220 is a billable diagnosis code used to specify a medical diagnosis of x-linked myotubular myopathy. The code G71.220 is valid during the fiscal year 2022 from October 01, 2021 through September 30, 2022 for the submission of HIPAA-covered transactions.
The ICD-10-CM code G71.220 might also be used to specify conditions or terms like myotubular myopathy, myotubular myopathy with type i atrophy or severe x-linked myotubular myopathy.
Tabular List of Diseases and Injuries
The Tabular List of Diseases and Injuries is a list of ICD-10 codes, organized "head to toe" into chapters and sections with coding notes and guidance for inclusions, exclusions, descriptions and more. The following references are applicable to the code G71.220:
Inclusion TermsInclusion Terms
These terms are the conditions for which that code is to be used. The terms may be synonyms of the code title, or, in the case of "other specified" codes, the terms are a list of the various conditions assigned to that code. The inclusion terms are not necessarily exhaustive. Additional terms found only in the Alphabetic Index may also be assigned to a code.
- Myotubular (centronuclear) myopathy
Index to Diseases and Injuries
The Index to Diseases and Injuries is an alphabetical listing of medical terms, with each term mapped to one or more ICD-10 code(s). The following references for the code G71.220 are found in the index:
The following clinical terms are approximate synonyms or lay terms that might be used to identify the correct diagnosis code:
- Myotubular myopathy
- Myotubular myopathy with type I atrophy
- Severe x-linked myotubular myopathy
- MYOPATHIES STRUCTURAL CONGENITAL-. a heterogeneous group of diseases characterized by the early onset of hypotonia developmental delay of motor skills non progressive weakness. each of these disorders is associated with a specific histologic muscle fiber abnormality.
G71220 replaces the following previously assigned ICD-10 code(s):