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- NCIT_C175047 IAO_0000115 "An autosomal dominant form of early infantile epileptic encephalopathy caused by mutation(s) in the KCNB1 gene, encoding potassium voltage-gated channel subfamily B member 1." @default.
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- NCIT_C175047 hasExactSynonym "DEE26" @default.
- NCIT_C175047 hasExactSynonym "Developmental and Epileptic Encephalopathy 26" @default.
- NCIT_C175047 hasExactSynonym "EIEE26" @default.
- NCIT_C175047 hasExactSynonym "Early Infantile Epileptic Encephalopathy 26" @default.
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