Other demyelinating diseases of central nervous system (G37) ICD-10-CM
The G37 code range covers other demyelinating diseases of central nervous system with 11 ICD-10-CM diagnosis codes. 9 of them are billable and valid for claim submission in fiscal year 2027, and the category headers group them but cannot themselves be billed.
Codes in the G37 Range 11 codes · 9 billable
- G37 Other demyelinating diseases of central nervous systemNon-billable
- G37.0 Diffuse sclerosis of central nervous system
- G37.1 Central demyelination of corpus callosum
- G37.2 Central pontine myelinolysis
- G37.3 Acute transverse myelitis in demyelinating disease of central nervous system
- G37.4 Subacute necrotizing myelitis of central nervous system
- G37.5 Concentric sclerosis [Balo] of central nervous system
- G37.8 Other specified demyelinating diseases of central nervous systemNon-billable
- G37.81 Myelin oligodendrocyte glycoprotein antibody disease
- G37.89 Other specified demyelinating diseases of central nervous system
- G37.9 Demyelinating disease of central nervous system, unspecified
Clinical Terms in This Code Range
Definitions from the National Library of Medicine for conditions coded in the G37 range.
Balo Concentric Sclerosis
A rare, rapidly progressive variant of multiple sclerosis. Characteristic findings of alternating bands of demyelinated and myelinated white matter in concentric layers may be seen throughout the central nervous system.
Demyelinating Disorder of Central Nervous System
Any condition in which there is degeneration of the myelin sheath that covers the nerves of the central nervous system.
Diffuse Cerebral Sclerosis of Schilder
A rare central nervous system demyelinating condition affecting children and young adults. Pathologic findings include a large, sharply defined, asymmetric focus of myelin destruction that may involve an entire lobe or cerebral hemisphere. The clinical course tends to be progressive and includes dementia, cortical blindness, cortical deafness, spastic hemiplegia, and pseudobulbar palsy. Concentric sclerosis of Balo is differentiated from diffuse cerebral sclerosis of Schilder by the pathologic finding of alternating bands of destruction and preservation of myelin in concentric rings. Alpers' Syndrome refers to a heterogeneous group of diseases that feature progressive cerebral deterioration and liver disease. (From Adams et al., Principles of Neurology, 6th ed, p914; Dev Neurosci 1991;13(4-5):267-73)
Marchiafava-Bignami Disease
A rare neurological disorder characterized initially by selective demyelination and necrosis of the corpus callosum. It is associated with chronic ethanol consumption or malnutrition, and depending on the acuity of presentation, signs and symptoms may include an altered mental state, motor disturbances, seizures, delirium and coma.
Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease
A disease in which serum antibodies are directed against MYELIN-OLIGODENDROCYTE GLYCOPROTEIN. MOGAD is typically associated with ACUTE DISSEMINATED ENCEPHALOMYELITIS; NEUROMYELITIS OPTICA; or TRANSVERSE MYELITIS.
Myelinolysis, Central Pontine
A demyelinating condition affecting the PONS and characterized clinically by an acute progressive QUADRIPLEGIA; DYSARTHRIA; DYSPHAGIA; and alterations of consciousness. Pathologic features include prominent demyelination in the central PONS with sparing of axons and neurons. This condition is usually associated with systemic disorders such as HYPONATREMIA; chronic ALCOHOLISM; LIVER FAILURE; severe BURNS; malignant NEOPLASMS; hemorrhagic PANCREATITIS; HEMODIALYSIS; and SEPSIS. The rapid medical correction of hyponatremia has been cited as a cause of this condition. (From Adams et al., Principles of Neurology, 6th ed, pp1125-6)
About the G37 Code Range
These conditions involve loss of myelin in the central nervous system. The subdivisions distinguish named diseases, affected structures, and whether a disease is specified.
G37.0 identifies diffuse sclerosis, while G37.5 identifies concentric sclerosis. G37.1 names the corpus callosum, and G37.2 names the central pons. The myelitis subdivisions distinguish acute transverse myelitis from subacute necrotizing myelitis.
G37.8 branches into G37.81 for myelin oligodendrocyte glycoprotein antibody disease and G37.89 for other specified diseases. G37.9 identifies an unspecified demyelinating disease of the central nervous system.
Questions About This Page
How many billable codes are in the G37 range?
Of the 11 codes in this range, 9 are billable and valid for claim submission from October 1, 2026 through September 30, 2027. Category header codes group them but cannot be reported on claims.
What does the G37 range classify?
The range classifies other demyelinating diseases of central nervous system. Each code links to its own reference page with billing status, MS-DRG grouping, coding notes, and clinical information.
Related References
Source: CMS FY 2027 ICD-10-CM Tabular List and order file, effective October 1, 2026 through September 30, 2027.