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- NCIT_C188139 IAO_0000115 "An autosomal dominant subtype of developmental and epileptic encephalopathy caused by mutation(s) in the SCN8A gene, encoding sodium channel protein type 8 subunit alpha." @default.
- NCIT_C188139 NCIT_NHC0 "C188139" @default.
- NCIT_C188139 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C188139 NCIT_P108 "Developmental and Epileptic Encephalopathy 13" @default.
- NCIT_C188139 NCIT_P207 "C3281191" @default.
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- NCIT_C188139 hasExactSynonym "DEE13" @default.
- NCIT_C188139 hasExactSynonym "Developmental and Epileptic Encephalopathy 13" @default.
- NCIT_C188139 hasExactSynonym "EIEE13" @default.
- NCIT_C188139 hasExactSynonym "Encephalopathy, Early Infantile, 13" @default.
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- NCIT_C188139 label "Developmental and Epileptic Encephalopathy 13" @default.
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