| Human Disease |
Term: Epilepsy, Nocturnal Frontal Lobe, 3; ENFL3
OMIM ID: 605375
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| Associated Genes |
Orthologous mouse and human markers where mutations in one or both species have been associated with phenotypes characteristic of this disease.
Mouse Gene |
Human Gene |
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Characteristics of this human disease are associated with mutations in... |
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 ...the human gene.
MGI data currently do not associate this disease with mutations in the orthologous mouse gene. |
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Transgenes and
other mutation types |
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Mouse Models
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1Models involving transgenes or other mutation types may also appear in other sections of the table.
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Analysis Tools