disease 1,759 words KG: ent-dise-9a1d57a2
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

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Related Hypotheses (6)

Oligodendrocyte White Matter Vulnerability
Score: 0.65
SASP-Driven Aquaporin-4 Dysregulation
Score: 0.78
Aquaporin-4 Polarization Rescue
Score: 0.73
Senescence-Associated Myelin Lipid Remodeling
Score: 0.73
Oligodendrocyte Protectin D1 Mimetic for Myelin Resolution
Score: 0.68

Related Analyses (18)

Neuroinflammation resolution mechanisms and pro-resolving me
neurodegeneration · archived
Blood-brain barrier transport mechanisms for antibody therap
neurodegeneration · archived
Gene expression changes in aging mouse brain predicting neur
neurodegeneration · completed
Senolytic therapy for age-related neurodegeneration
neurodegeneration · archived
Astrocyte reactivity subtypes in neurodegeneration
neurodegeneration · completed

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

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