ICD-10-CM 2027 diagnosis code
G71.0Muscular dystrophy
G71.0 is a header code, so it can't be reported by itself. Choose one of the 5 more specific codes beneath it.
Code last changed in FY2019 (effective October 1, 2018). Source: official FY2027 ICD-10-CM release from CDC/NCHS and CMS. Page updated September 29, 2026. About our data
About G71.0
G71.0 is the ICD-10-CM diagnosis code for muscular dystrophy. It belongs to category G71 (primary disorders of muscles), block G70-G73 (diseases of myoneural junction and muscle) and chapter 6 (diseases of the nervous system). It is a header code, so it can't be reported by itself; one of its 5 subcodes must be used instead.
Within G71 (primary disorders of muscles), G71.0 is specifically for muscular dystrophy. Related codes cover myotonic disorders (G71.1), congenital myopathies (G71.2), mitochondrial myopathy, not elsewhere classified (G71.3), other primary disorders of muscles (G71.8) and primary disorder of muscle, unspecified (G71.9).
To report this condition, pick the subcode that matches the documentation: G71.00 (unspecified), G71.01 (dystrophy), G71.02 (dystrophy), G71.03 (dystrophies) and G71.09 (dystrophies).
It has been part of ICD-10-CM since the code set took effect on October 1, 2015, and changed in FY2019 (expanded into subcodes).
Before ICD-10, this condition was coded in ICD-9-CM as 359.1 (hereditary progressive muscular dystrophy).
Specific codes under G71.0
- G71.00Muscular dystrophy, unspecifiedBillable
- G71.01Duchenne or Becker muscular dystrophyBillable
- G71.02Facioscapulohumeral muscular dystrophyBillable
- G71.03Limb girdle muscular dystrophies
- G71.031Autosomal dominant limb girdle muscular dystrophyBillable
- G71.032Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunctionBillable
- G71.033Limb girdle muscular dystrophy due to dysferlin dysfunctionBillable
- G71.034Limb girdle muscular dystrophy due to sarcoglycan dysfunction
- G71.0340Limb girdle muscular dystrophy due to sarcoglycan dysfunction, unspecifiedBillable
- G71.0341Limb girdle muscular dystrophy due to alpha sarcoglycan dysfunctionBillable
- G71.0342Limb girdle muscular dystrophy due to beta sarcoglycan dysfunctionBillable
- G71.0349Limb girdle muscular dystrophy due to other sarcoglycan dysfunctionBillable
- G71.035Limb girdle muscular dystrophy due to anoctamin-5 dysfunctionBillable
- G71.036Limb girdle muscular dystrophy due to fukutin related protein dysfunctionBillable
- G71.038Other limb girdle muscular dystrophyBillable
- G71.039Limb girdle muscular dystrophy, unspecifiedBillable
- G71.09Other specified muscular dystrophiesBillable
Notes that apply from higher levels
Instructions written at a parent level also apply to G71.0.
Broader instructions also apply from Chapter 6: Diseases of the nervous system.
Codes whose notes reference G71.0
- Z99.3Code first
ICD-9-CM equivalent
Converter →- 359.1Hereditary progressive muscular dystrophyexact
From the CMS 2018 General Equivalence Mappings (GEMs), the final GEMs release.
Code history
- 2016
- 2017
- 2018
- 2019
- 2020
- 2021
- 2022
- 2023
- 2024
- 2025
- 2026
- 2027
- FY2016 (effective 10/1/2015): Added (first year of ICD-10-CM)
- FY2019 (effective 10/1/2018): Expanded — no longer billable