G71.11
BillableMyotonic muscular dystrophy
Myotonic muscular dystrophy
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Dystrophia myotonica [Steinert]
- Myotonia atrophica
- Myotonic dystrophy
- Proximal myotonic myopathy (PROMM)
- Steinert disease
Excludes 2
Conditions not included here, but the patient may have both
- •certain conditions originating in the perinatal periodP04-P96
- •certain infectious and parasitic diseasesA00-B99
- •complications of pregnancy, childbirth and the puerperiumO9A)O00
- •congenital malformations, deformations, and chromosomal abnormalitiesQ00-Q99
- •endocrine, nutritional and metabolic diseasesE00-E88
- •injury, poisoning and certain other consequences of external causesS00-T88
- •neoplasmsC00-D49
- •symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classifiedR00-R94
- •arthrogryposis multiplex congenitaQ74.3
- •metabolic disordersE70-E88
- •myositisM60
Related Codes(4)
Also Known As / Clinical Terms(191)
SNOMED CT
- Dilated cardiomyopathy due to myotonic dystrophy2816000
- Dilated cardiomyopathy secondary to myotonic dystrophy2816000
- Dilated cardiomyopathy due to muscular dystrophy28869005
- Dilated cardiomyopathy secondary to muscular dystrophy28869005
- Myotonic dystrophy type 177956009
- Steinert disease77956009
- Steinert myotonic dystrophy syndrome77956009
- Steinert syndrome77956009
- Cardiomyopathy in myotonic dystrophy195031006
- Congenital myotonic dystrophy240104008
- Congenital-onset Steinert disease240104008
- Congenital-onset Steinert myotonic dystrophy240104008
- Congenital-onset myotonic dystrophy type 1240104008
- Dystrophia myotonica facies248201006
- Myotonic dystrophy type 2715317001
- Proximal myotonic myopathy715317001
- Ricker disease715317001
- Ricker syndrome715317001
- DM - dystrophia myotonica1177122009
- Dystrophia myotonica1177122009
- Myotonia dystrophica1177122009
- Myotonic dystrophy1177122009
- Adult-onset Steinert disease1366414003
- Adult-onset Steinert myotonic dystrophy1366414003
- Adult-onset myotonic dystrophy type 11366414003
- Childhood-onset Steinert disease1366415002
- Childhood-onset Steinert myotonic dystrophy1366415002
- Childhood-onset myotonic dystrophy type 11366415002
- Juvenile-onset Steinert disease1366416001
- Juvenile-onset Steinert myotonic dystrophy1366416001
- Juvenile-onset myotonic dystrophy type 11366416001
- Late-onset Steinert disease1366417005
- Late-onset Steinert myotonic dystrophy1366417005
- Late-onset myotonic dystrophy type 11366417005
UMLS
- Atrophica, MyotoniaC0027126
- Atrophicas, MyotoniaC0027126
- DM - dystrophia myotonicaC0027126
- Disease, SteinertC0027126
- Disease, Steinert'sC0027126
- Dystrophia MyotonicaC0027126
- Dystrophia Myotonica 1C0027126
- Dystrophia MyotonicasC0027126
- Dystrophia myotonicaC0027126
- Dystrophia myotonica [Steinert]C0027126
- Dystrophica, MyotoniaC0027126
- Dystrophicas, MyotoniaC0027126
- Dystrophies, MyotonicC0027126
- Dystrophy, MyotonicC0027126
- Dystrophy, Steinert MyotonicC0027126
- Myotonia AtrophicaC0027126
- Myotonia AtrophicasC0027126
- Myotonia DystrophicaC0027126
- Myotonia DystrophicasC0027126
- Myotonia atrophicaC0027126
- Myotonia dystrophicaC0027126
- Myotonic DystrophiesC0027126
- Myotonic DystrophyC0027126
- Myotonic Dystrophy 1C0027126
- Myotonic Dystrophy, SteinertC0027126
- Myotonic dystrophyC0027126
- Myotonic dystrophy (disorder)C0027126
- Myotonic muscular dystrophyC0027126
- Myotonica, DystrophiaC0027126
- Myotonicas, DystrophiaC0027126
- STEINERT DISC0027126
- STEINERTS DISC0027126
- Steinert DiseaseC0027126
- Steinert Myotonic DystrophyC0027126
- Steinert diseaseC0027126
- Steinert's DiseaseC0027126
- Steinert's diseaseC0027126
- Steinerts DiseaseC0027126
- disease steinertsC0027126
- dystrophia myotonicaC0027126
- dystrophy muscular myotonicC0027126
- dystrophy myotonicC0027126
- muscular dystrophy myotonicC0027126
- myotonia atrophicaC0027126
- myotonia dystrophicaC0027126
- myotonic dystrophyC0027126
- myotonic muscular dystrophyC0027126
- steinert diseaseC0027126
- steinert syndromeC0027126
- steinert's diseaseC0027126
- syndrome steinertC0027126
- DM2C2931689
- DYSTROPHIA MYOTONICA 2C2931689
- Dystrophia Myotonica 2C2931689
- Dystrophia Myotonica 2sC2931689
- MYOTONIC DYSTROPHY 2C2931689
- MYOTONIC MYOPATHY, PROXIMALC2931689
- Myopathies, Proximal MyotonicC2931689
- Myopathy, Proximal MyotonicC2931689
- Myotonic Dystrophy 2C2931689
- Myotonic Myopathies, ProximalC2931689
- Myotonic Myopathy, ProximalC2931689
- Myotonic dystrophy type 2C2931689
- PROMMC2931689
- PROMM (Proximal Myotonic Myopathy)C2931689
- PROMMs (Proximal Myotonic Myopathy)C2931689
- PROXIMAL MYOTONIC MYOPATHYC2931689
- Proximal Myotonic MyopathiesC2931689
- Proximal Myotonic MyopathyC2931689
- Proximal myotonic myopathyC2931689
- Proximal myotonic myopathy (PROMM)C2931689
- Proximal myotonic myopathy (disorder)C2931689
- RICKER SYNDROMEC2931689
- Ricker SyndromeC2931689
- Ricker diseaseC2931689
- Ricker syndromeC2931689
- Syndrome, RickerC2931689
Clinical Terms
- Dystrophica, Myotonia
- Proximal myotonic myopathy (disorder)
- Childhood-onset Steinert myotonic dystrophy
- Proximal Myotonic Myopathies
- Myotonica, Dystrophia
- Myotonic Dystrophy 1
- Steinert's Disease
- Congenital myotonic dystrophy
- dystrophy myotonic
- STEINERTS DIS
- Myotonic Dystrophy 2
- Ricker syndrome
- Dilated cardiomyopathy due to muscular dystrophy
- Myotonic Myopathy, Proximal
- Disease, Steinert
- Atrophicas, Myotonia
- disease steinerts
- PROXIMAL MYOTONIC MYOPATHY
- Childhood-onset Steinert disease
- STEINERT DIS
- PROMM
- Congenital-onset Steinert myotonic dystrophy
- Myotonia Dystrophicas
- Late-onset myotonic dystrophy type 1
- steinert syndrome
- Late-onset Steinert disease
- Dilated cardiomyopathy secondary to myotonic dystrophy
- Myotonic Dystrophy
- Juvenile-onset Steinert myotonic dystrophy
- Dystrophia Myotonicas
- Myotonia atrophica
- dystrophia myotonica
- Myopathies, Proximal Myotonic
- Steinert myotonic dystrophy syndrome
- Disease, Steinert's
- Myotonic Dystrophy, Steinert
- Dystrophy, Steinert Myotonic
- Myotonic dystrophy type 1
- PROMMs (Proximal Myotonic Myopathy)
- Dystrophicas, Myotonia
- PROMM (Proximal Myotonic Myopathy)
- Dilated cardiomyopathy due to myotonic dystrophy
- Syndrome, Ricker
- Dystrophia Myotonica 2
- Congenital-onset Steinert disease
- Proximal myotonic myopathy (PROMM)
- Steinerts Disease
- Ricker disease
- DM2
- dystrophy muscular myotonic
- Myotonia Atrophicas
- steinert disease
- Dystrophia Myotonica 2s
- Late-onset Steinert myotonic dystrophy
- Dystrophies, Myotonic
- Dystrophy, Myotonic
- Dilated cardiomyopathy secondary to muscular dystrophy
- Myotonia dystrophica
- Adult-onset Steinert disease
- Dystrophia myotonica facies
- Cardiomyopathy in myotonic dystrophy
- Myotonic Dystrophies
- Dystrophia Myotonica 1
- Dystrophia myotonica [Steinert]
- Adult-onset myotonic dystrophy type 1
- Myopathy, Proximal Myotonic
- Myotonicas, Dystrophia
- Steinert Myotonic Dystrophy
- Childhood-onset myotonic dystrophy type 1
- Congenital-onset myotonic dystrophy type 1
- Juvenile-onset myotonic dystrophy type 1
- syndrome steinert
- Myotonic dystrophy type 2
- Myotonic dystrophy (disorder)
- Atrophica, Myotonia
- DM - dystrophia myotonica
- Myotonic Myopathies, Proximal
- Adult-onset Steinert myotonic dystrophy
- Juvenile-onset Steinert disease
- muscular dystrophy myotonic
Frequently Asked Questions
What is the ICD-10 code for myotonic muscular dystrophy?
The ICD-10-CM code for myotonic muscular dystrophy is G71.11. The full clinical description is "Myotonic muscular dystrophy". G71.11 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G71.11 mean?
ICD-10-CM code G71.11 represents “Myotonic muscular dystrophy”. It is classified under Chapter 6: Diseases of the Nervous System and is a billable/specific code that can be used on a claim.
Is G71.11 a billable code?
Yes, G71.11 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G71.11 in?
G71.11 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What SNOMED CT codes does G71.11 map to?
G71.11 maps to 12 SNOMED CT concepts: 1366414003, 195031006, 1366415002, 240104008, 1177122009, and 7 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G71.11?
G71.11 is linked to 2 UMLS Concept Unique Identifiers: C0027126, C2931689. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does G71.11 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like myotonic muscular dystrophy affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of G71.11?
There is no direct ICD-11 mapping available for G71.11 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.