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 period (P04-P96)
- certain infectious and parasitic diseases (A00-B99)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
- arthrogryposis multiplex congenita (Q74.3)
- metabolic disorders (E70-E88)
- myositis (M60.-)
Also Known As / Clinical Terms
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
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.
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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.