2026 ICD-10-CM Diagnosis Code G35.D

Multiple sclerosis, unspecified

ICD-10-CM Code:
G35.D
ICD-10 Code for:
Multiple sclerosis, unspecified
Is Billable?
Yes - Valid for Submission
Code Navigator:

G35.D is a billable diagnosis code used to specify a medical diagnosis of multiple sclerosis, unspecified. The code is valid during the current fiscal year for the submission of HIPAA-covered transactions from October 01, 2025 through September 30, 2026.

Unspecified diagnosis codes like G35.D are acceptable when clinical information is unknown or not available about a particular condition. Although a more specific code is preferable, unspecified codes should be used when such codes most accurately reflect what is known about a patient's condition. Specific diagnosis codes should not be used if not supported by the patient's medical record.

Code Classification

  • Diseases of the nervous system
    G00–G99
    • Demyelinating diseases of the central nervous system
      G35-G37
      • Multiple sclerosis
        G35

Approximate Synonyms

The following list of clinical terms are approximate synonyms, alternative descriptions, or common phrases that might be used by patients, healthcare providers, or medical coders to describe the same condition. These synonyms and related diagnosis terms are often used when searching for an ICD-10 code, especially when the exact medical terminology is unclear. Whether you're looking for lay terms, similar diagnosis names, or common language alternatives, this list can help guide you to the correct ICD-10 classification.

  • Acute relapsing multiple sclerosis
  • Autonomic disorder due to multiple sclerosis
  • Autonomic nervous system disorder co-occurrent and due to neurodegenerative disorder
  • Benign multiple sclerosis
  • Brown-Séquard syndrome due to multiple sclerosis
  • Central neuropathic pain
  • Chorea due to immunological disorder
  • Chronic central neuropathic pain
  • Chronic central neuropathic pain due to multiple sclerosis
  • Cognitive impairment due to multiple sclerosis
  • Cognitive impairment due to multiple sclerosis
  • Dementia associated with multiple sclerosis
  • Dementia associated with multiple sclerosis
  • Dementia due to multiple sclerosis with altered behavior
  • Demyelination of spinal cord
  • Demyelination of spinal cord
  • Exacerbation of multiple sclerosis
  • Functional quadriplegia due to multiple sclerosis
  • Hemichorea
  • Hemichorea due to multiple sclerosis
  • Intermediate uveitis
  • Lamellar ichthyosis
  • Malignant multiple sclerosis
  • Marburg acute multiple sclerosis
  • Multiple sclerosis
  • Multiple sclerosis associated intermediate uveitis
  • Multiple sclerosis of the brainstem
  • Multiple sclerosis of the spinal cord
  • Multiple sclerosis of the spinal cord
  • Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome
  • Myelitis due to multiple sclerosis
  • Optic neuritis due to demyelinating disease
  • Pediatric multiple sclerosis
  • Posterior cord syndrome due to multiple sclerosis
  • Progressive multiple sclerosis
  • Progressive relapsing multiple sclerosis
  • Retrobulbar neuritis
  • Retrobulbar neuritis due to multiple sclerosis

Clinical Information

  • Multiple Sclerosis

    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)
  • Multiple Sclerosis, Chronic Progressive

    a form of multiple sclerosis characterized by a progressive deterioration in neurologic function which is in contrast to the more typical relapsing remitting form. if the clinical course is free of distinct remissions, it is referred to as primary progressive multiple sclerosis. when the progressive decline is punctuated by acute exacerbations, it is referred to as progressive relapsing multiple sclerosis. the term secondary progressive multiple sclerosis is used when relapsing remitting multiple sclerosis evolves into the chronic progressive form. (from ann neurol 1994;36 suppl:s73-s79; adams et al., principles of neurology, 6th ed, pp903-914)
  • Multiple Sclerosis, Relapsing-Remitting

    the most common clinical variant of multiple sclerosis, characterized by recurrent acute exacerbations of neurologic dysfunction followed by partial or complete recovery. common clinical manifestations include loss of visual (see optic neuritis), motor, sensory, or bladder function. acute episodes of demyelination may occur at any site in the central nervous system, and commonly involve the optic nerves, spinal cord, brain stem, and cerebellum. (adams et al., principles of neurology, 6th ed, pp903-914)
  • ABCA12 wt Allele|ABC12|ARCI4A|ARCI4B|ATP Binding Cassette Subfamily A Member 12 wt Allele|ATP-Binding Cassette, Sub-Family A (ABC1), Member 12 Gene|ATP-Binding Cassette, Subfamily A, Member 12 Gene|DKFZP434G232|ICR2B|Ichthyosis Congenita II, Lamellar Ichthyosis B Gene|LI2

    human abca12 wild-type allele is located in the vicinity of 2q35 and is approximately 207 kb in length. this allele, which encodes glucosylceramide transporter abca12 protein, plays a role in both the membrane localization of glucosylceramide and other lipids in lamellar granules and in cholesterol transport. mutation of the gene is associated with autosomal recessive congenital ichthyosis (arci) types 4a and 4b (harlequin).
  • Lamellar Ichthyosis

    a very rare, autosomal recessive inherited skin disorder present at birth. it is characterized by the presence of a transparent membrane encasing the newborn. this membrane sheds in about two weeks after birth to reveal generalized scaling and skin erythema.

New 2026 ICD-10-CM Code

G35.D is new to ICD-10-CM code set for the FY 2026, effective October 1, 2025. The National Center for Health Statistics (NCHS) has published an update to the ICD-10-CM diagnosis codes which became effective October 1, 2025. This is a new and revised code for the FY 2026 (October 1, 2025 - September 30, 2026).

Tabular List of Diseases and Injuries

The following annotation back-references are applicable to this diagnosis code. The Tabular List of Diseases and Injuries is a list of ICD-10-CM codes, organized "head to toe" into chapters and sections with coding notes and guidance for inclusions, exclusions, descriptions and more.


Inclusion Terms

Inclusion Terms
These terms are the conditions for which that code is to be used. The terms may be synonyms of the code title, or, in the case of "other specified" codes, the terms are a list of the various conditions assigned to that code. The inclusion terms are not necessarily exhaustive. Additional terms found only in the Alphabetic Index may also be assigned to a code.
  • Disseminated multiple sclerosis
  • Generalized multiple sclerosis
  • Multiple sclerosis NOS
  • Multiple sclerosis of brain stem
  • Multiple sclerosis of cord

Index to Diseases and Injuries References

The following annotation back-references for this diagnosis code are found in the injuries and diseases index. The Index to Diseases and Injuries is an alphabetical listing of medical terms, with each term mapped to one or more ICD-10-CM code(s).

Index of External Cause of Injuries

References found for this diagnosis code in the External Cause of Injuries Index:

    • Dementia(degenerative (primary)) (persisting) (unspecified severity) (without behavioral disturbance, psychotic disturbance, mood disturbance, and anxiety)
      • in (due to)
        • multiple
          • sclerosis
    • Dementia(degenerative (primary)) (persisting) (unspecified severity) (without behavioral disturbance, psychotic disturbance, mood disturbance, and anxiety)
      • in (due to)
        • multiple
          • sclerosis
            • with behavioral disturbance
    • Demyelination, demyelinization
      • global
    • Disease, diseased
      • demyelinating, demyelinizating (nervous system)
        • multiple sclerosis
    • Myelosclerosis
      • disseminated, of nervous system
    • Sclérose en plaques
    • Sclerosis, sclerotic
      • ascending multiple
    • Sclerosis, sclerotic
      • brain (generalized) (lobular)
        • disseminated
    • Sclerosis, sclerotic
      • brain (generalized) (lobular)
        • insular
    • Sclerosis, sclerotic
      • brain (generalized) (lobular)
        • miliary
    • Sclerosis, sclerotic
      • brain (generalized) (lobular)
        • multiple
    • Sclerosis, sclerotic
      • brain (generalized) (lobular)
        • stem, multiple
    • Sclerosis, sclerotic
      • bulbar, multiple
    • Sclerosis, sclerotic
      • cerebrospinal (disseminated) (multiple)
    • Sclerosis, sclerotic
      • combined (spinal cord)
        • multiple
    • Sclerosis, sclerotic
      • disseminated
    • Sclerosis, sclerotic
      • dorsal
    • Sclerosis, sclerotic
      • insular
    • Sclerosis, sclerotic
      • multiple (brain stem) (cerebral) (disseminated) (generalized) (spinal cord)
    • Sclerosis, sclerotic
      • plaques
    • Sclerosis, sclerotic
      • spinal (cord) (progressive)
        • combined
          • multiple
    • Sclerosis, sclerotic
      • spinal (cord) (progressive)
        • disseminated
    • Sclerosis, sclerotic
      • spinal (cord) (progressive)
        • multiple

Replacement Code

G35D replaces the following previously assigned ICD-10-CM code(s):

  • G35 - Multiple sclerosis

Code History

  • FY 2026 - Code Added, effective from 10/1/2025 through 9/30/2026