G71.19
BillableOther specified myotonic disorders
Other specified myotonic disorders
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Myotonia fluctuans
- Myotonia permanens
- Neuromyotonia [Isaacs]
- Paramyotonia congenita (of von Eulenburg)
- Pseudomyotonia
- Symptomatic myotonia
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(147)
SNOMED CT
- Myotonia3434004
- Myotonus3434004
- Tonic spasm of muscle3434004
- Eulenburg disease41574007
- Eulenburg syndrome41574007
- Eulenburg's disease41574007
- Paramyotonia congenita41574007
- Axonal neuropathy60703000
- Myotonic cataract64741003
- Isaacs syndrome80138003
- Isaacs-Mertens syndrome80138003
- Peripheral axonal neuropathy128208007
- Myotonic disorder193237003
- Infantile myotonia193238008
- Cataract in systemic disorders231970007
- Eye closing finding301991004
- Eye closing observation301991004
- Continuous muscle fiber activity305719002
- Continuous muscle fibre activity305719002
- Neuromyotonia305719002
- Finding of movement of eyelid366010006
- Movement of eyelid - finding366010006
- Myotonic warm-up phenomenon422410004
- Eye closure myotonia422485001
- Myotonic warm-up phenomenon - hand grip422561007
- Non dystrophic myotonia424795008
- Potassium aggravated myotonia702355008
- Sodium channel myotonia702355008
- Rippling muscle disease709281006
- Rippling muscle syndrome709281006
- Autosomal recessive axonal neuropathy with neuromyotonia711406009
- Autosomal recessive neuromyotonia with axonal neuropathy711406009
- Gamstorp-Wohlfart syndrome711406009
- Myokymia, myotonia and muscle wasting711406009
- Exercise induced delayed onset myotonia715788001
- Fluctuating myotonia715788001
- Myotonia fluctuans715788001
- Myotonia permanens715789009
- Pseudomyotonia762666001
- Acquired rippling muscle disease770596007
- Immune-mediated rippling muscle disease770596007
- Rippling muscle disease with myasthenia gravis770596007
- Paradoxical myotonia1137401000
- Percussion myotonia1137402007
UMLS
- EULENBURG DISC0221055
- EULENBURGS DISC0221055
- Eulenburg DiseaseC0221055
- Eulenburg diseaseC0221055
- Eulenburg syndromeC0221055
- Eulenburg's DiseaseC0221055
- Eulenburg's diseaseC0221055
- PARALYSIS PERIODICA PARAMYOTONICAC0221055
- PARAMYOTONIA CONGENC0221055
- PARAMYOTONIA CONGENITAC0221055
- PARAMYOTONIA CONGENITA OF VON EULENBURGC0221055
- PMCC0221055
- Paralysis Periodica ParamyotoniaC0221055
- Paralysis periodica paramyotoniaC0221055
- Paramyotonia CongenitaC0221055
- Paramyotonia Congenita of von EulenbergC0221055
- Paramyotonia Congenita of von EulenburgC0221055
- Paramyotonia congenitaC0221055
- Paramyotonia congenita (disorder)C0221055
- Paramyotonia congenita (of von Eulenburg)C0221055
- Paramyotonia congenita of von EulenburgC0221055
- Von Eulenberg DiseaseC0221055
- Von Eulenberg's DiseaseC0221055
- Von Eulenberg's diseaseC0221055
- eulenburg's diseaseC0221055
- paramyotonia congenitaC0221055
- Exercise induced delayed onset myotoniaC0752355
- Exercise-Induced Delayed-Onset MyotoniaC0752355
- Fluctuating myotoniaC0752355
- MYOTONIA FLUCTUANSC0752355
- Myotonia FluctuansC0752355
- Myotonia fluctuansC0752355
- Myotonia fluctuans (disorder)C0752355
- MYOTONIA PERMANENSC5848361
- Myotonia permanensC5848361
- Myotonia permanens (disorder)C5848361
- Neuromyotonia [Isaacs]C2875314
- Other specified myotonic disordersC0410224
- PseudomyotoniaC4521481
- Pseudomyotonia (finding)C4521481
- Symptomatic myotoniaC1404544
Clinical Terms
- Myotonia fluctuans
- Axonal neuropathy
- Eye closing observation
- Immune-mediated rippling muscle disease
- Movement of eyelid - finding
- Non dystrophic myotonia
- MYOTONIA PERMANENS
- PMC
- Von Eulenberg's Disease
- PARALYSIS PERIODICA PARAMYOTONICA
- Von Eulenberg Disease
- Paramyotonia Congenita
- Paramyotonia congenita (of von Eulenburg)
- Percussion myotonia
- PARAMYOTONIA CONGENITA OF VON EULENBURG
- Potassium aggravated myotonia
- Myotonus
- Rippling muscle disease
- Autosomal recessive axonal neuropathy with neuromyotonia
- Eulenburg Disease
- Eulenburg's Disease
- Peripheral axonal neuropathy
- Eulenburg syndrome
- Sodium channel myotonia
- Myotonia
- EULENBURG DIS
- Eye closing finding
- Rippling muscle syndrome
- Symptomatic myotonia
- Continuous muscle fibre activity
- Isaacs syndrome
- EULENBURGS DIS
- Myotonic warm-up phenomenon - hand grip
- Pseudomyotonia
- Cataract in systemic disorders
- Tonic spasm of muscle
- Myokymia, myotonia and muscle wasting
- Exercise-Induced Delayed-Onset Myotonia
- Myotonic disorder
- Paralysis Periodica Paramyotonia
- Paramyotonia Congenita of von Eulenberg
- Rippling muscle disease with myasthenia gravis
- Fluctuating myotonia
- Infantile myotonia
- Neuromyotonia
- Paradoxical myotonia
- Exercise induced delayed onset myotonia
- Gamstorp-Wohlfart syndrome
- Myotonia permanens (disorder)
- Myotonic cataract
- Acquired rippling muscle disease
- Myotonia fluctuans (disorder)
- Eye closure myotonia
- PARAMYOTONIA CONGEN
- Finding of movement of eyelid
- Isaacs-Mertens syndrome
- Myotonic warm-up phenomenon
- Autosomal recessive neuromyotonia with axonal neuropathy
- Pseudomyotonia (finding)
- Continuous muscle fiber activity
- Neuromyotonia [Isaacs]
- Paramyotonia congenita (disorder)
Frequently Asked Questions
What is the ICD-10 code for other specified myotonic disorders?
The ICD-10-CM code for other specified myotonic disorders is G71.19. The full clinical description is "Other specified myotonic disorders". G71.19 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G71.19 mean?
ICD-10-CM code G71.19 represents “Other specified myotonic disorders”. 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 G71.19 a billable code?
Yes, G71.19 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G71.19 in?
G71.19 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What SNOMED CT codes does G71.19 map to?
G71.19 maps to 25 SNOMED CT concepts: 770596007, 711406009, 60703000, 231970007, 305719002, and 20 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G71.19?
G71.19 is linked to 7 UMLS Concept Unique Identifiers: C0221055, C0752355, C5848361, C2875314, C0410224, and 2 more. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does G71.19 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other specified myotonic disorders 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 G71.19?
There is no direct ICD-11 mapping available for G71.19 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.