2024 ICD-10-CM Diagnosis Code G71.031
Autosomal dominant limb girdle muscular dystrophy
- ICD-10-CM Code:
- G71.031
- ICD-10 Code for:
- Autosomal dominant limb girdle muscular dystrophy
- Is Billable?
- Yes - Valid for Submission
- Chronic Condition Indicator: [1]
- Chronic
- Code Navigator:
G71.031 is a billable diagnosis code used to specify a medical diagnosis of autosomal dominant limb girdle muscular dystrophy. The code is valid during the current fiscal year for the submission of HIPAA-covered transactions from October 01, 2023 through September 30, 2024.
Approximate Synonyms
The following clinical terms are approximate synonyms or lay terms that might be used to identify the correct diagnosis code:
- Autosomal dominant limb girdle muscular dystrophy type 1A
- Autosomal dominant limb girdle muscular dystrophy type 1D
- Autosomal dominant limb girdle muscular dystrophy type 1E
- Autosomal dominant limb girdle muscular dystrophy type 1F
- Autosomal dominant limb girdle muscular dystrophy type 1G
- Autosomal dominant limb-girdle muscular dystrophy type 1H
- Autosomal dominant muscular dystrophy with limb girdle distribution
Clinical Classification
Clinical Category is Myopathies
- CCSR Category Code: NVS018
- Inpatient Default CCSR: Y - Yes, default inpatient assignment for principal diagnosis or first-listed diagnosis.
- Outpatient Default CCSR: Y - Yes, default outpatient assignment for principal diagnosis or first-listed diagnosis.
Tabular List of Diseases and Injuries
The following annotation back-references are applicable to this diagnosis code. The Tabular List of Diseases and Injuries is a list of ICD-10-CM codes, organized "head to toe" into chapters and sections with coding notes and guidance for inclusions, exclusions, descriptions and more.
Inclusion Terms
Inclusion TermsThese 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.
- LGMD D4 calpain-3-related
- LGMD D5 collagen 6-related
- Limb girdle muscular dystrophy type 1
Index to Diseases and Injuries References
The following annotation back-references for this diagnosis code are found in the injuries and diseases index. The Index to Diseases and Injuries is an alphabetical listing of medical terms, with each term mapped to one or more ICD-10-CM code(s).
- - Calpainopathy (primary) - G71.032
- - autosomal dominant - G71.031
- - Dystrophy, dystrophia
- - muscular - G71.00
- - limb-girdle - G71.039
- - D1 (autosomal dominant) - G71.031
- - D2 (autosomal dominant) - G71.031
- - D3 (autosomal dominant) - G71.031
- - D4 (autosomal dominant) - G71.031
- - D5 (autosomal dominant) - G71.031
- - type 1 (autosomal dominant) - G71.031
- - type 1A (autosomal dominant) - G71.031
- - type 1B (autosomal dominant) - G71.031
- - type 1C (autosomal dominant) - G71.031
- - type 1E (autosomal dominant) - G71.031
- - type 1H (autosomal dominant) - G71.031
- - type 1I (autosomal dominant) - G71.031
- - limb-girdle - G71.039
- - muscular - G71.00
Replacement Code
G71031 replaces the following previously assigned ICD-10-CM code(s):
- G71.09 - Other specified muscular dystrophies
Code History
- FY 2024 - No Change, effective from 10/1/2023 through 9/30/2024
- FY 2023 - Code Added, effective from 10/1/2022 through 9/30/2023
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.