DRG 058

Multiple sclerosis and cerebellar ataxia with mcc

  • G11.0
    Congenital nonprogressive ataxia
  • G11.1
    Early-onset cerebellar ataxia
  • G11.2
    Late-onset cerebellar ataxia
  • G11.3
    Cerebellar ataxia with defective DNA repair
  • G11.4
    Hereditary spastic paraplegia
  • G11.8
    Other hereditary ataxias
  • G11.9
    Hereditary ataxia, unspecified
  • G32.81
    Cerebellar ataxia in diseases classified elsewhere
  • G35
    Multiple sclerosis
  • G36.0
    Neuromyelitis optica [Devic]
  • G36.1
    Acute and subacute hemorrhagic leukoencephalitis [Hurst]
  • G36.8
    Other specified acute disseminated demyelination
  • G36.9
    Acute disseminated demyelination, unspecified
  • G37.0
    Diffuse sclerosis of central nervous system
  • G37.1
    Central demyelination of corpus callosum
  • G37.2
    Central pontine myelinolysis
  • G37.5
    Concentric sclerosis [Balo] of central nervous system
  • G37.8
    Other specified demyelinating diseases of central nervous system
  • G37.9
    Demyelinating disease of central nervous system, unspecified
ICD-10-CM G11.0

Congenital nonprogressive ataxia

    2016 2017 2018 2019 2020 Billable/Specific Code
ICD-10-CM G11.1

Early-onset cerebellar ataxia

    2016 2017 2018 2019 2020 Billable/Specific Code
Applicable To
  • Early-onset cerebellar ataxia with essential tremor
  • Early-onset cerebellar ataxia with myoclonus [Hunt's ataxia]
  • Early-onset cerebellar ataxia with retained tendon reflexes
  • Friedreich's ataxia (autosomal recessive)
  • X-linked recessive spinocerebellar ataxia
ICD-10-CM G11.2

Late-onset cerebellar ataxia

    2016 2017 2018 2019 2020 Billable/Specific Code Adult Dx (15-124 years)
ICD-10-CM G11.3

Cerebellar ataxia with defective DNA repair

    2016 2017 2018 2019 2020 Billable/Specific Code
Applicable To
  • Ataxia telangiectasia [Louis-Bar]
Type 2 Excludes
  • Cockayne's syndrome (Q87.19)
  • other disorders of purine and pyrimidine metabolism (E79.-)
  • xeroderma pigmentosum (Q82.1)
ICD-10-CM G11.4

Hereditary spastic paraplegia

    2016 2017 2018 2019 2020 Billable/Specific Code
ICD-10-CM G11.8

Other hereditary ataxias

    2016 2017 2018 2019 2020 Billable/Specific Code
ICD-10-CM G11.9

Hereditary ataxia, unspecified

    2016 2017 2018 2019 2020 Billable/Specific Code
Applicable To
  • Hereditary cerebellar ataxia NOS
  • Hereditary cerebellar degeneration
  • Hereditary cerebellar disease
  • Hereditary cerebellar syndrome
ICD-10-CM G32.81

Cerebellar ataxia in diseases classified elsewhere

    2016 2017 2018 2019 2020 Billable/Specific Code Manifestation Code
Code First
  • underlying disease, such as:
  • celiac disease (with gluten ataxia) (K90.0)
  • cerebellar ataxia (in) neoplastic disease (paraneoplastic cerebellar degeneration) (C00-D49)
  • non-celiac gluten ataxia (M35.9)
Type 1 Excludes
  • systemic atrophy primarily affecting the central nervous system in alcoholic cerebellar ataxia (G31.2)
  • systemic atrophy primarily affecting the central nervous system in myxedema (G13.2)
ICD-10-CM G35

Multiple sclerosis

    2016 2017 2018 2019 2020 Billable/Specific Code
Applicable To
  • Disseminated multiple sclerosis
  • Generalized multiple sclerosis
  • Multiple sclerosis NOS
  • Multiple sclerosis of brain stem
  • Multiple sclerosis of cord
ICD-10-CM G36.0

Neuromyelitis optica [Devic]

    2016 2017 2018 2019 2020 Billable/Specific Code
Applicable To
  • Demyelination in optic neuritis
Type 1 Excludes
  • optic neuritis NOS (H46)
ICD-10-CM G36.1

Acute and subacute hemorrhagic leukoencephalitis [Hurst]

    2016 2017 2018 2019 2020 Billable/Specific Code
ICD-10-CM G36.8

Other specified acute disseminated demyelination

    2016 2017 2018 2019 2020 Billable/Specific Code
ICD-10-CM G36.9

Acute disseminated demyelination, unspecified

    2016 2017 2018 2019 2020 Billable/Specific Code
ICD-10-CM G37.0

Diffuse sclerosis of central nervous system

    2016 2017 2018 2019 2020 Billable/Specific Code
Applicable To
  • Periaxial encephalitis
  • Schilder's disease
Type 1 Excludes
  • X linked adrenoleukodystrophy (E71.52-)
ICD-10-CM G37.1

Central demyelination of corpus callosum

    2016 2017 2018 2019 2020 Billable/Specific Code
ICD-10-CM G37.2

Central pontine myelinolysis

    2016 2017 2018 2019 2020 Billable/Specific Code
ICD-10-CM G37.5

Concentric sclerosis [Balo] of central nervous system

    2016 2017 2018 2019 2020 Billable/Specific Code
ICD-10-CM G37.8

Other specified demyelinating diseases of central nervous system

    2016 2017 2018 2019 2020 Billable/Specific Code
ICD-10-CM G37.9

Demyelinating disease of central nervous system, unspecified

    2016 2017 2018 2019 2020 Billable/Specific Code