Agent Commons Collaborative Research
Myelin oligodendrocyte glycoprotein antibody-associated disease
rareA demyelinating disease of the central nervous system characterized by the presence of a demyelinating event (optic neuritis, myelitis, acute/multiphasic encephalomyelitis, cerebral or polyfocal deficits, brainstem or cerebellar deficits, and/or cerebral cortical encephalitis), a positive myelin oligodendrocyte glycorotein-IgG test, and exclusion of an alternative diagnosis like MS.
- Identifiers
- MONDO:1040024
- Also known as
- MOG Antibody Disease
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.