G25.3
BillableMyoclonus
Myoclonus
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Drug-induced myoclonus
- Palatal myoclonus
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
- •sleep related movement disordersG47.6
Use Additional Code
Additional codes that should follow this code
Related Codes(9)
G25.0Essential tremor
G25.1Drug-induced tremor
G25.2Other specified forms of tremor
G25.4Drug-induced chorea
G25.5Other chorea
G25.6Drug induced tics and other tics of organic origin
G25.7Other and unspecified drug induced movement disorders
G25.8Other specified extrapyramidal and movement disorders
G25.9Extrapyramidal and movement disorder, unspecified
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(216)
SNOMED CT
- Diabetes mellitus associated with genetic syndrome5969009
- Genetic syndromes of diabetes mellitus5969009
- Palatal myoclonus9366002
- Palatal nystagmus9366002
- Myoclonia17450006
- Myoclonus17450006
- Hyperekplexia19557000
- Hyperexplexia19557000
- Startle syndrome19557000
- Action myoclonus27572006
- Intention myoclonus27572006
- Dysphonia of palatopharyngolaryngeal myoclonus30736009
- Pendular nystagmus35743001
- Paramyoclonus multiplex60935008
- Essential myoclonus67305007
- Familial essential myoclonus67305007
- Nerve conduction deafness73371001
- Nerve deafness73371001
- Neural hearing loss73371001
- Retrocochlear hearing loss73371001
- Juvenile cerebellar degeneration AND myoclonus76156000
- Disorder characterised by myoclonus127324008
- Disorder characterized by myoclonus127324008
- Myoclonic disorder127324008
- Myoclonus disorder127324008
- Progressive cerebellar ataxia with palatal myoclonus230239001
- Post-anoxic myoclonus230344005
- Postencephalitic myoclonus230345006
- Drug-induced myoclonus230346007
- Segmental cord myoclonus230347003
- Palatal-tympanic myoclonus230348008
- Hyoid myoclonus230349000
- Opsoclonus-myoclonus syndrome230350000
- Herrmann syndrome237612000
- Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction237612000
- Stapedial finding250899001
- Stapedial observation250899001
- Oculopalatal myoclonus307672008
- Spontaneous eye movements in coma307690009
- Vertical myoclonus307693006
- Benign neonatal sleep myoclonus413638006
- Periodic limb movement disorder418763003
- Myoclonus of stapedius muscle426187002
- Stapedial myoclonus426187002
- Non-epileptic myoclonus427111000
- Myoclonus of tensor tympani muscle427789001
- Myoclonus tensor tympani muscle427789001
- Tensor tympani myoclonus427789001
- Febrile myoclonus441604003
- Myoclonus associated with fever441604003
- Hypnic jerk443438009
- Hypnic twitch443438009
- Periodic leg movements of sleep445140006
- Brainstem myoclonus698738000
- Cerebral cortex myoclonus698835006
- Cortical myoclonus698835006
- Spinal cord myoclonus698836007
- Spinal myoclonus698836007
- Segmental myoclonus722974003
- Focal myoclonus724773004
- Myoclonus, cerebellar ataxia, deafness syndrome733065003
- Familial cortical myoclonus763770005
- Familial myoclonus of cerebral cortex763770005
- Sporadic hyperekplexia783705006
- Dissociative neurological symptom disorder co-occurrent with myoclonus788910003
- Functional neurological symptom disorder with myoclonus788910003
- Propriospinal myoclonus at sleep onset789010008
- Autoimmune opsoclonus myoclonus838323002
- Infantile propriospinal myoclonus at sleep onset1052285005
- Propriospinal myoclonus at sleep onset in infancy1052285005
- Autoimmune generalised polymyoclonus1208833001
- Autoimmune generalized polymyoclonus1208833001
- Opsoclonus myoclonus syndrome due to paraneoplastic syndrome1231185005
- Paraneoplastic opsoclonus myoclonus syndrome1231185005
- Myoclonus due to paraneoplastic syndrome1231233002
- Paraneoplastic myoclonus1231233002
- Autoimmune disorder of movement1259084000
- Autoimmune movement disorder1259084000
- Myoclonic disorder due to uraemia1263501007
- Myoclonic disorder due to uremia1263501007
- Myoclonic disorder due to sialidosis1263503005
- Myoclonic disorder due to mitochondrial cytopathy1263505003
- Myoclonic disorder due to mitochondrial disorder1263505003
- Myoclonic disorder due to neuronal ceroid lipofuscinosis1263506002
- Myoclonic disorder due to hepatic failure1263507006
- Myoclonic disorder due to dementia1263512007
- Insomnia due to periodic limb movement disorder93681000119102
- Sleep related movement disorder84991000119105
UMLS
- Drug-induced myoclonusC0393622
- Drug-induced myoclonus (disorder)C0393622
- Involuntary jerking movementsC0027066
- Jerk, MyoclonicC0027066
- Jerking, MyoclonicC0027066
- Jerks, MyoclonicC0027066
- MyocloniaC0027066
- Myoclonic JerkC0027066
- Myoclonic JerkingC0027066
- Myoclonic JerksC0027066
- Myoclonic jerksC0027066
- MyoclonusC0027066
- Myoclonus (finding)C0027066
- involuntary muscle jerkingC0027066
- myoclonic disorderC0027066
- myoclonic jerkC0027066
- myoclonic jerkingC0027066
- myoclonic jerksC0027066
- myoclonusC0027066
- Myoclonus, PalatalC0030214
- Palatal MyoclonusC0030214
- Palatal myoclonusC0030214
- Palatal myoclonus (disorder)C0030214
- Palatal nystagmusC0030214
- Palatal tremorC0030214
- myoclonus palatalC0030214
- palatal myoclonusC0030214
Clinical Terms
- Benign neonatal sleep myoclonus
- Opsoclonus myoclonus syndrome due to paraneoplastic syndrome
- Myoclonic Jerk
- Genetic syndromes of diabetes mellitus
- Neural hearing loss
- Drug-induced myoclonus
- Familial essential myoclonus
- Cortical myoclonus
- Sporadic hyperekplexia
- Jerking, Myoclonic
- Myoclonus associated with fever
- Drug-induced myoclonus (disorder)
- Myoclonic disorder due to uraemia
- Myoclonic disorder due to uremia
- Progressive cerebellar ataxia with palatal myoclonus
- Vertical myoclonus
- Myoclonia
- Infantile propriospinal myoclonus at sleep onset
- myoclonic disorder
- Febrile myoclonus
- Opsoclonus-myoclonus syndrome
- Autoimmune movement disorder
- Diabetes mellitus associated with genetic syndrome
- Myoclonus tensor tympani muscle
- Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction
- Stapedial finding
- Myoclonic jerks
- Spontaneous eye movements in coma
- Post-anoxic myoclonus
- Startle syndrome
- Palatal nystagmus
- Sleep related movement disorder
- Autoimmune opsoclonus myoclonus
- Involuntary jerking movements
- Familial myoclonus of cerebral cortex
- Myoclonic Jerking
- Functional neurological symptom disorder with myoclonus
- Palatal-tympanic myoclonus
- Juvenile cerebellar degeneration AND myoclonus
- Oculopalatal myoclonus
- Jerks, Myoclonic
- Propriospinal myoclonus at sleep onset
- myoclonus palatal
- Hyperexplexia
- Periodic leg movements of sleep
- Pendular nystagmus
- Familial cortical myoclonus
- Dysphonia of palatopharyngolaryngeal myoclonus
- Brainstem myoclonus
- Postencephalitic myoclonus
- involuntary muscle jerking
- Paraneoplastic myoclonus
- Disorder characterized by myoclonus
- Non-epileptic myoclonus
- Nerve deafness
- Dissociative neurological symptom disorder co-occurrent with myoclonus
- Autoimmune generalized polymyoclonus
- Myoclonic disorder due to sialidosis
- Hyoid myoclonus
- Stapedial myoclonus
- Myoclonus of stapedius muscle
- Tensor tympani myoclonus
- Paraneoplastic opsoclonus myoclonus syndrome
- Myoclonic disorder due to mitochondrial disorder
- Cerebral cortex myoclonus
- Segmental cord myoclonus
- Essential myoclonus
- Myoclonus, cerebellar ataxia, deafness syndrome
- Hyperekplexia
- Insomnia due to periodic limb movement disorder
- Myoclonic disorder due to neuronal ceroid lipofuscinosis
- Segmental myoclonus
- Autoimmune generalised polymyoclonus
- Periodic limb movement disorder
- Spinal myoclonus
- Hypnic twitch
- Myoclonic disorder due to hepatic failure
- Palatal myoclonus (disorder)
- Myoclonic disorder due to dementia
- Palatal tremor
- Action myoclonus
- Spinal cord myoclonus
- Myoclonus, Palatal
- Myoclonic disorder due to mitochondrial cytopathy
- Palatal myoclonus
- Propriospinal myoclonus at sleep onset in infancy
- Myoclonus of tensor tympani muscle
- Stapedial observation
- Intention myoclonus
- Hypnic jerk
- Autoimmune disorder of movement
- Myoclonus disorder
- Retrocochlear hearing loss
- Disorder characterised by myoclonus
- Paramyoclonus multiplex
- Jerk, Myoclonic
- Nerve conduction deafness
- Myoclonus (finding)
- Myoclonus due to paraneoplastic syndrome
- Focal myoclonus
- Herrmann syndrome
Frequently Asked Questions
What is the ICD-10 code for myoclonus?
The ICD-10-CM code for myoclonus is G25.3. The full clinical description is "Myoclonus". G25.3 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G25.3 mean?
ICD-10-CM code G25.3 represents “Myoclonus”. 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 G25.3 a billable code?
Yes, G25.3 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G25.3 in?
G25.3 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What codes cannot be used with G25.3?
G25.3 has Excludes1 notes indicating codes that cannot be used together with it, including: facial myokymia (G51.4); myoclonic epilepsy (G40.-).
Are additional codes required with G25.3?
Yes, when using G25.3, also report: adverse effect, if applicable, to identify drug (T36-T50 with fifth or sixth character 5).
What SNOMED CT codes does G25.3 map to?
G25.3 maps to 57 SNOMED CT concepts: 27572006, 1259084000, 1208833001, 838323002, 413638006, and 52 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G25.3?
G25.3 is linked to 3 UMLS Concept Unique Identifiers: C0393622, C0027066, C0030214. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does G25.3 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like myoclonus 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 G25.3?
G25.3 maps to the ICD-11 code: 8A06.Z (Myoclonic disorders, unspecified).
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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.