G70.00
BillableMyasthenia gravis without (acute) exacerbation
Myasthenia gravis without (acute) exacerbation
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Myasthenia gravis NOS
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
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
Related Codes(1)
Also Known As / Clinical Terms(97)
SNOMED CT
- Toxic disorders of the neuromuscular junction17940001
- Toxic myoneural junction disorder17940001
- Toxic neuromuscular junction disorder17940001
- Myasthenia gravis, adult form31839002
- Myasthenia gravis, juvenile form55051001
- Neonatal myasthenia gravis82178003
- Erb-Goldflam disease91637004
- MG - Myasthenia gravis91637004
- Myasthenia gravis91637004
- Persistent neonatal myasthenia gravis193206003
- Juvenile or adult myasthenia gravis193207007
- Genetically determined myasthenia230669004
- Congenital myasthenia230672006
- Congenital myasthenia syndrome230672006
- Congenital myasthenic syndrome230672006
- Putative defect in acetylcholine synthesis or packaging230676009
- Congenital end-plate acetylcholinesterase deficiency230677000
- Decrease of MEPP amplitude without acetylcholine receptor deficiency230678005
- Decrease of motor end-plate potential amplitude without acetylcholine receptor deficiency230678005
- Abnormality of synaptic vesicles230679002
- Ocular myasthenia230684008
- Myasthenia gravis associated with thymoma230685009
- Generalised myasthenia230686005
- Generalized myasthenia230686005
- Myasthenic myopathy230687001
- Myopathy in myasthenia gravis230687001
- Deficiency of acetylcholinesterase360586005
- Deficiency of choline esterase I360586005
- Deficiency of true cholinesterase360586005
- Neonatal neuromuscular disorder363222009
- Ocular myasthenia with strabismus414927004
- Rippling muscle disease709281006
- Rippling muscle syndrome709281006
- Acquired rippling muscle disease770596007
- Immune-mediated rippling muscle disease770596007
- Rippling muscle disease with myasthenia gravis770596007
- Myasthenia gravis caused by MuSK (muscle-specific kinase) antibodies521000146105
- Myasthenia gravis caused by muscle-specific tyrosine kinase antibodies521000146105
- Myasthenia gravis in remission16415791000119104
- Myasthenia gravis without exacerbation77471000119103
UMLS
- Erb-Goldflam diseaseC0026896
- MG - Myasthenia gravisC0026896
- MYASTHENIA GRAVISC0026896
- Myasthenia GravisC0026896
- Myasthenia gravisC0026896
- Myasthenia gravis (disorder)C0026896
- Myasthenia gravis NOSC0026896
- Myasthenia gravis paralyticaC0026896
- myasthenia gravisC0026896
- myasthenia gravis (MG)C0026896
- myasthenia gravis disorderC0026896
- Myasthenia gravis without (acute) exacerbationC1260409
Clinical Terms
- Congenital myasthenia syndrome
- Immune-mediated rippling muscle disease
- Myasthenic myopathy
- Myasthenia gravis NOS
- Juvenile or adult myasthenia gravis
- Decrease of MEPP amplitude without acetylcholine receptor deficiency
- MYASTHENIA GRAVIS
- Congenital myasthenia
- Rippling muscle disease
- Congenital myasthenic syndrome
- Myopathy in myasthenia gravis
- Myasthenia gravis in remission
- Myasthenia gravis paralytica
- Genetically determined myasthenia
- Rippling muscle syndrome
- Generalised myasthenia
- Myasthenia gravis, juvenile form
- Abnormality of synaptic vesicles
- Myasthenia gravis, adult form
- Congenital end-plate acetylcholinesterase deficiency
- Erb-Goldflam disease
- Myasthenia gravis caused by muscle-specific tyrosine kinase antibodies
- Myasthenia gravis caused by MuSK (muscle-specific kinase) antibodies
- Myasthenia gravis without exacerbation
- Rippling muscle disease with myasthenia gravis
- Toxic myoneural junction disorder
- Toxic neuromuscular junction disorder
- Neonatal neuromuscular disorder
- Decrease of motor end-plate potential amplitude without acetylcholine receptor deficiency
- Toxic disorders of the neuromuscular junction
- myasthenia gravis (MG)
- Neonatal myasthenia gravis
- Ocular myasthenia
- Acquired rippling muscle disease
- Deficiency of true cholinesterase
- Generalized myasthenia
- MG - Myasthenia gravis
- Myasthenia gravis (disorder)
- Persistent neonatal myasthenia gravis
- Ocular myasthenia with strabismus
- Myasthenia gravis associated with thymoma
- Deficiency of acetylcholinesterase
- Putative defect in acetylcholine synthesis or packaging
- Deficiency of choline esterase I
- myasthenia gravis disorder
Frequently Asked Questions
What is the ICD-10 code for myasthenia gravis without (acute) exacerbation?
The ICD-10-CM code for myasthenia gravis without (acute) exacerbation is G70.00. The full clinical description is "Myasthenia gravis without (acute) exacerbation". G70.00 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G70.00 mean?
ICD-10-CM code G70.00 represents “Myasthenia gravis without (acute) exacerbation”. 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 G70.00 a billable code?
Yes, G70.00 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G70.00 in?
G70.00 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What codes cannot be used with G70.00?
G70.00 has Excludes1 notes indicating codes that cannot be used together with it, including: botulism (A05.1, A48.51-A48.52); transient neonatal myasthenia gravis (P94.0).
What SNOMED CT codes does G70.00 map to?
G70.00 maps to 25 SNOMED CT concepts: 230679002, 770596007, 230677000, 230672006, 230678005, and 20 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G70.00?
G70.00 is linked to 2 UMLS Concept Unique Identifiers: C0026896, C1260409. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does G70.00 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like myasthenia gravis without (acute) exacerbation 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 G70.00?
There is no direct ICD-11 mapping available for G70.00 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.