G71.12
BillableMyotonia congenita
Myotonia congenita
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Acetazolamide responsive myotonia congenita
- Dominant myotonia congenita [Thomsen disease]
- Myotonia levior
- Recessive myotonia congenita [Becker 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
- Myotonia levior8960007
- Becker myotonia congenita20305008
- Congenital myotonia, autosomal recessive form20305008
- Myotonia congenita - autosomal recessive form20305008
- Congenital myotonia, autosomal dominant form57938005
- Myotonia congenita - autosomal dominant form57938005
- Thomsen myotonia congenita57938005
- Thomsen's disease57938005
- Potassium aggravated myotonia702355008
- Sodium channel myotonia702355008
- Acetazolamide responsive myotonia715793003
- Congenital myotonia726051002
- Myotonia congenita726051002
- Myotonia, intellectual disability, skeletal anomalies syndrome782941005
- Richieri Costa-da Silva syndrome782941005
UMLS
- Acetazolamide responsive myotonia congenitaC2931826
- MYOTONIA CONGENITA, ACETAZOLAMIDE-RESPONSIVEC2931826
- MYOTONIA CONGENITA, ATYPICALC2931826
- MYOTONIA PERMANENSC2931826
- MYOTONIA, POTASSIUM-AGGRAVATEDC2931826
- Myotonia congenita, acetazolamide-responsiveC2931826
- Myotonia congenita, atypicalC2931826
- Myotonia, Potassium-AggravatedC2931826
- PAMC2931826
- Potassium Aggravated MyotoniaC2931826
- Potassium aggravated myotoniaC2931826
- Potassium aggravated myotonia (disorder)C2931826
- Potassium-Aggravated MyotoniaC2931826
- Potassium-aggravated myotoniaC2931826
- SODIUM CHANNEL MUSCLE DISEASEC2931826
- Sodium Channel MyotoniaC2931826
- Sodium channel myotoniaC2931826
- BATTEN-TURNER CONGENITAL MYOPATHYC0027127
- Batten Turner Congenital MyopathyC0027127
- Batten-Turner Congenital MyopathyC0027127
- Congenital MyotoniaC0027127
- Congenital myotoniaC0027127
- Generalized MyotoniaC0027127
- Generalized MyotoniasC0027127
- MYOTONIA CONGENC0027127
- Myopathy, CongenitalC0027127
- Myotonia CongenitaC0027127
- Myotonia congenitaC0027127
- Myotonia congenita (disorder)C0027127
- Myotonia congenitalC0027127
- Myotonia, GeneralizedC0027127
- Myotonias, GeneralizedC0027127
- BECKER DISEASEC0751360
- Becker DiseaseC0751360
- Becker Generalized MyotoniaC0751360
- Becker myotonia congenitaC0751360
- Congenital myotonia, autosomal recessive formC0751360
- Congenital myotonia, autosomal recessive form (disorder)C0751360
- Disease, BeckerC0751360
- Generalized Myotonia of BeckerC0751360
- Generalized Myotonia, BeckerC0751360
- MYOTONIA CONGENITA, AUTOSOMAL RECESSIVEC0751360
- MYOTONIA, GENERALIZEDC0751360
- Myotonia Congenita, Autosomal RecessiveC0751360
- Myotonia congenita - autosomal recessive formC0751360
- Myotonia, Becker GeneralizedC0751360
- Myotonia, Generalized, BeckerC0751360
- Recessive myotonia congenita [Becker disease]C0751360
- Congenital myotonia, autosomal dominant formC2936781
- Congenital myotonia, autosomal dominant form (disorder)C2936781
- Disease, ThomsenC2936781
- Disease, Thomsen'sC2936781
- Disease, ThomsensC2936781
- Dominant myotonia congenita [Thomsen disease]C2936781
- Generalized Myotonia of ThomsenC2936781
- MYOTONIA CONGENITA, AUTOSOMAL DOMINANTC2936781
- Myotonia Congenita, Autosomal DominantC2936781
- Myotonia congenita - autosomal dominant formC2936781
- THDC2936781
- THOMSEN DISC2936781
- THOMSEN DISEASEC2936781
- THOMSENS DISC2936781
- Thomsen DiseaseC2936781
- Thomsen Generalized MyotoniaC2936781
- Thomsen myotonia congenitaC2936781
- Thomsen's DiseaseC2936781
- Thomsen's diseaseC2936781
- Thomsens DiseaseC2936781
- myotonia congenitaC2936781
- thomsen diseaseC2936781
- thomsen's diseaseC2936781
- thomsens diseaseC2936781
- MYOTONIA LEVIORC0270959
- Myotonia LeviorC0270959
- Myotonia leviorC0270959
- Myotonia levior (disorder)C0270959
Frequently Asked Questions
What is the ICD-10 code for myotonia congenita?
The ICD-10-CM code for myotonia congenita is G71.12. The full clinical description is "Myotonia congenita". G71.12 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G71.12 mean?
ICD-10-CM code G71.12 represents "Myotonia congenita". 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 G71.12 a billable code?
Yes, G71.12 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G71.12 in?
G71.12 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What SNOMED CT codes does G71.12 map to?
G71.12 maps to 7 SNOMED CT concepts: 715793003, 20305008, 726051002, 57938005, 8960007, and 2 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G71.12?
G71.12 is linked to 5 UMLS Concept Unique Identifiers: C2931826, C0027127, C0751360, C2936781, C0270959. 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.