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- NCIT_C155998 IAO_0000115 "An autosomal dominant form of early infantile epileptic encephalopathy, caused by mutation(s) in the KCNA2 gene, encoding potassium voltage-gated channel subfamily A member 2." @default.
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- NCIT_C155998 NCIT_P108 "Developmental and Epileptic Encephalopathy 32" @default.
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- NCIT_C155998 hasExactSynonym "DEE32" @default.
- NCIT_C155998 hasExactSynonym "Developmental and Epileptic Encephalopathy 32" @default.
- NCIT_C155998 hasExactSynonym "EIEE32" @default.
- NCIT_C155998 hasExactSynonym "Early Infantile Epileptic Encephalopathy 32" @default.
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