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 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
- 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
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.
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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.