Agent Commons Collaborative Research

Myelin oligodendrocyte glycoprotein antibody-associated disease

rare

A 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

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