- G71.11 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2024 edition of ICD-10-CM G71.11 became effective on October 1, 2022.
- This is the American ICD-10-CM version of G71.11 – other international versions of ICD-10 G71.11 may differ.
ICD-10-CM G71.11 is grouped within Diagnostic Related Group(s):
- 091 Other disorders of nervous system with mcc
- 092 Other disorders of nervous system with cc
- 093 Other disorders of nervous system without cc/mcc
Applicable To
- Dystrophia myotonica [Steinert]
- Myotonia atrophica
- Myotonic dystrophy
- Proximal myotonic myopathy (PROMM)
- Steinert disease
Code History
- 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
- 2016 (effective 10/1/2015): No change
- 2017 (effective 10/1/2016): No change
- 2018 (effective 10/1/2017): No change
- 2019 (effective 10/1/2018): No change
- 2020 (effective 10/1/2019): No change
- 2021 (effective 10/1/2020): No change
- 2022 (effective 10/1/2021): No change
- 2024 (effective 10/1/2022): No change
Diagnosis Index entries containing back-references to G71.11:
- myotonic > muscle, muscular (diffuse) (general) (idiopathic) (primary) M62.50
- myotonia > Atrophy, atrophic (of)
- myotonia atrophica > due to I42.6
- Batten-Steinert > Disease, diseased
- Curschmann > Disease, diseased
- Steinert\’s > Disease, diseased
- myotonic > congenital (hereditary) (progressive) (with specific morphological abnormalities of the muscle fiber) G71.09
- myotonic > muscular G71.00
- myotonic, myotonica > Dystrophy, dystrophia
- myotonia atrophica > in (due to) E51.12
- mytonic, proximal (PROMM) > Myopathy G72.9
- proximal myotonic (PROMM) > Myopathy G72.9
- atrophica > Myotonia (acquisita) (intermittens) M62.89
- dystrophica > Myotonia (acquisita) (intermittens) M62.89
- Batten-Steinert > Syndrome
- Curschmann (-Batten) (-Steinert) > Syndrome