Version May 2024
| Inflammatory disease |
| Acute disseminated encephalomyelitis |
| Behçet disease |
| Chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids |
| Clinically isolated syndromes suggestive of multiple sclerosis |
| Myelin oligodendrocyte glycoprotein antibody-associated disease |
| Neuromyelitis optica spectrum disorder |
| Paraneoplastic encephalomyelopathies |
| Polyarteritis nodosa |
| Primary angiitis of the central nervous system |
| Sjögren's disease |
| Systemic lupus erythematosus |
| Infectious disease |
| Human immunodeficiency virus |
| Lyme neuroborreliosis |
| Neurosyphilis |
| Progressive multifocal leukoencephalopathy |
| HTLV-1-associated myelopathy/Tropical spastic paraparesis |
| Genetic disease |
| Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy |
| Granulomatous disease |
| Lymphomatoid granulomatosis |
| Sarcoidosis |
| Granulomatosis with polyangiitis (Wegener's) |
| Disease of myelin |
| Adrenoleukodystrophy |
| Adult metachromatic leukodystrophy |
| Other |
| Arnold-Chiari malformation |
| Compressive spinal cord lesions |
| Vascular malformations |
| Vitamin B12 deficiency |
| Spinocerebellar disorders |
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