disease 1,759 words KG: ent-dise-9a1d57a2 2026-03-24
kind:diseasesection:diseasesstate:published
Contents

Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD)

Disease Info
Prevalence1-5 per 100,000 population 3
Incidence0.5-2 per million per year
Age distributionBimodal—peaks in childhood (median: 7 years) and adulthood (median: 35 years)
Gender distributionMore common in males in childhood; female predominance in adults
EthnicityNo strong ethnic predominance, unlike NMOSD
FunctionCell adhesion molecule, involved in:
ExpressionOligodendrocyte surface, myelin sheaths
ImmunogenicityHighly species-conserved, targets for demyelinating antibodies
IsotypePredominantly IgG1 (can fix complement)
TargetConformational epitopes on extracellular domain of MOG
Primary oligodendrocyte injuryDirect demyelination
Less complement activationMOG antibodies are less potent activators
DatabasesOMIMOrphanetClinicalTrialsPubMed

Knowledge Graph

Related Hypotheses (6)

Oligodendrocyte White Matter Vulnerability
Score: 0.40
SASP-Driven Aquaporin-4 Dysregulation
Score: 0.59
Aquaporin-4 Polarization Rescue
Score: 0.51
Glymphatic System-Enhanced Antibody Clearance Reversal
Score: 0.54
Senescence-Associated Myelin Lipid Remodeling
Score: 0.51

Related Analyses (21)

Blood-brain barrier transport mechanisms for antibody therap
neurodegeneration · archived
Senolytic therapy for age-related neurodegeneration
neurodegeneration · archived
Neuroinflammation resolution mechanisms and pro-resolving me
neurodegeneration · archived
Gene expression changes in aging mouse brain predicting neur
neurodegeneration · archived
TREM2 agonism vs antagonism in DAM microglia
neurodegeneration · failed

Related Experiments (3)

CSF Dynamic Biomarkers for Differential Diagnosis of NPH vs
clinical · proposed · Score: 0.90
CSF Dynamic Biomarkers for Differential Diagnosis of NPH vs
clinical · proposed · Score: 0.40
NPH Glymphatic System Interaction Experiment
clinical · proposed · Score: 0.40