Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations MECP2 disease C1968556 GeneticVariation 0.72 disgenet
Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations MECP2 disease C1968556 Biomarker 0.72 disgenet
Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations MECP2 disease C1968556 CausalMutation 0.72 disgenet
Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations MECP2 disease C1968556 GermlineCausalMutation 0.72 disgenet
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