| Human Disease |
Term: Epileptic Encephalopathy, Early Infantile, 2; EIEE2
OMIM ID: 300672
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| Synonyms |
Infantile Spasm Syndrome, X-Linked 2; ISSX2; Rett Syndrome, Atypical, Cdkl5-Related; Rett Syndrome, Variant, with Infantile Spasms |
| 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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Analysis Tools