2022 ICD-10-CM Diagnosis Code G35: Multiple Sclerosis
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2026
- ICD-10-CM Codes ›
- G00-G99 ›
- G35-G37 ›
- G35- ›
- 2026 ICD-10-CM Diagnosis Code G35
Multiple sclerosis
- 2016 2017 2018 2019 2020 2021 2022 2023 2024 2025 2026 - Converted to Parent Code Non-Billable/Non-Specific Code
- G35 should not be used for reimbursement purposes as there are multiple codes below it that contain a greater level of detail.
- ICD-10-CM G35 is a new 2026 ICD-10-CM code that became effective on October 1, 2025.
- This is the American ICD-10-CM version of G35 - other international versions of ICD-10 G35 may differ.
- Applicable To annotations, or
- Code Also annotations, or
- Code First annotations, or
- Excludes1 annotations, or
- Excludes2 annotations, or
- Includes annotations, or
- Note annotations, or
- Use Additional annotations
- G00-G99 2026 ICD-10-CM Range G00-G99
Diseases of the nervous systemType 2 Excludes
- 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)
- Chronic progressive multiple sclerosis
- Dementia due to multiple sclerosis w behavioral disturbance
- Dementia due to multiple sclerosis with altered behavior
- Dementia from multiple sclerosis
- Exacerbation of multiple sclerosis
- Multiple sclerosis (ms), chronic/progressive
- Multiple sclerosis (ms), exacerbation
- Multiple sclerosis (ms), primary progressive
- Multiple sclerosis (ms), relapsing progressive
- Multiple sclerosis (ms), relapsing remitting
- Multiple sclerosis (ms), secondary progressive
- Primary progressive multiple sclerosis
- Relapsing remitting multiple sclerosis
- Remittent-progressive multiple sclerosis
- Secondary progressive multiple sclerosis
- A disorder of the central nervous system marked by weakness, numbness, a loss of muscle coordination, and problems with vision, speech, and bladder control. Multiple sclerosis is thought to be an autoimmune disease in which the body's immune system destroys myelin. Myelin is a substance that contains both protein and fat (lipid), serving as a nerve insulator and helping in the transmission of nerve signals.
- A progressive autoimmune disorder affecting the central nervous system resulting in demyelination. Patients develop physical and cognitive impairments that correspond with the affected nerve fibers.
- An autoimmune disorder mainly affecting young adults and characterized by destruction of myelin in the central nervous system. Pathologic findings include multiple sharply demarcated areas of demyelination throughout the white matter of the central nervous system. Clinical manifestations include visual loss, extra-ocular movement disorders, paresthesias, loss of sensation, weakness, dysarthria, spasticity, ataxia, and bladder dysfunction. The usual pattern is one of recurrent attacks followed by partial recovery (see multiple sclerosis, relapsing-remitting), but acute fulminating and chronic progressive forms (see multiple sclerosis, chronic progressive) also occur. (Adams et al., Principles of Neurology, 6th ed, p903)
- Chronic disease characterized by presence of numerous areas of demyelination in the central nervous system with symptoms such as weakness, incoordination, paresthesis, and speech disturbances; the etiology is unknown.
- Multiple sclerosis (ms) is a nervous system disease that affects your brain and spinal cord. It damages the myelin sheath, the material that surrounds and protects your nerve cells. This damage slows down or blocks messages between your brain and your body, leading to the symptoms of ms. They can include
- visual disturbances
- muscle weakness
- trouble with coordination and balance
- sensations such as numbness, prickling, or "pins and needles"
- thinking and memory problems
- 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
- 2017 (effective 10/1/2016): No change
- 2018 (effective 10/1/2017): No change
- 2019 (effective 10/1/2018): No change
- 2020 (effective 10/1/2019): No change
- 2021 (effective 10/1/2020): No change
- 2022 (effective 10/1/2021): No change
- 2023 (effective 10/1/2022): No change
- 2024 (effective 10/1/2023): No change
- 2025 (effective 10/1/2024): No change
- 2026 (effective 10/1/2025): Deleted code
- 2026 (effective 10/1/2025): New code
- Code First: F02, F48.2 ICD-10-CM Diagnosis Code F02
Dementia in other diseases classified elsewhere
- 2016 2017 2018 2019 2020 2021 2022 2023 2024 2025 2026 Non-Billable/Non-Specific Code
- the underlying physiological condition, such as:
- Alzheimer's (G30.-)
- cerebral lipidosis (E75.4)
- Creutzfeldt-Jakob disease (A81.0-)
- epilepsy and recurrent seizures (G40.-)
- frontotemporal dementia (G31.09)
- hepatolenticular degeneration (E83.01)
- human immunodeficiency virus [HIV] disease (B20)
- Huntington's disease (G10)
- hypercalcemia (E83.52)
- hypothyroidism, acquired (E00-E03.-)
- intoxications (T36-T65)
- Jakob-Creutzfeldt disease (A81.0-)
- multiple sclerosis (G35-)
- neurocognitive disorder with Lewy bodies (G31.83)
- neurosyphilis (A52.17)
- niacin deficiency [pellagra] (E52)
- other frontotemporal neurocognitive disorder (G31.90)
- Parkinson's disease (G20.-)
- Pick's disease (G31.01)
- polyarteritis nodosa (M30.0)
- prion disease (A81.9)
- systemic lupus erythematosus (M32.-)
- traumatic brain injury (S06.-)
- trypanosomiasis (B56.-, B57.-)
- vitamin B deficiency (E53.8)
- Major neurocognitive disorder in other diseases classified elsewhere
- mild neurocognitive disorder due to known physiological condition with or without behavioral disturbance (F06.7-)
- dementia in alcohol and psychoactive substance disorders (F10-F19, with .17, .27, .97)
- vascular dementia (F01.5-, F01.A-, F01.B-, F01.C-)
Pseudobulbar affect
- 2016 2017 2018 2019 2020 2021 2022 2023 2024 2025 2026 Billable/Specific Code
- Involuntary emotional expression disorder
- underlying cause, if known, such as:
- amyotrophic lateral sclerosis (G12.21)
- multiple sclerosis (G35-)
- sequelae of cerebrovascular disease (I69.-)
- sequelae of traumatic intracranial injury (S06.-)
- Type 1 Excludes: G37.3 ICD-10-CM Diagnosis Code G37.3
Acute transverse myelitis in demyelinating disease of central nervous system
- 2016 2017 2018 2019 2020 2021 2022 2023 2024 2025 2026 Billable/Specific Code
- Acute transverse myelitis NOS
- Acute transverse myelopathy
- acute flaccid myelitis (G04.82)
- multiple sclerosis (G35-)
- neuromyelitis optica [Devic] (G36.0)
- Type 2 Excludes: G04 ICD-10-CM Diagnosis Code G04
Encephalitis, myelitis and encephalomyelitis
- 2016 2017 2018 2019 2020 2021 2022 2023 2024 2025 2026 Non-Billable/Non-Specific Code
- acute ascending myelitis
- meningoencephalitis
- meningomyelitis
- encephalopathy NOS (G93.40)
- acute transverse myelitis (G37.3)
- alcoholic encephalopathy (G31.2)
- multiple sclerosis (G35-)
- myalgic encephalomyelitis (G93.32)
- subacute necrotizing myelitis (G37.4)
- toxic encephalitis (G92.8)
- toxic encephalopathy (G92.8)
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
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