FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term developmental and epileptic encephalopathy 103 ID (Ontology) DOID:0070389 (Human Disease)
Definition A developmental and epileptic encephalopathy characterized by onset of various types of seizures in the first year of life that has_material_basis_in heterozygous mutation in the KCNC2 gene on chromosome 12q21.
Also Known As "DEE103" ; "early infantile epileptic encephalopathy 103"
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 Genes
 developmental and epileptic encephalopathy 103       2
 for disease ribbon | developmental and epileptic encephalopathy 103       2
 model of | developmental and epileptic encephalopathy 103       2
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electroclinical syndrome
 |__developmental and epileptic encephalopathy__
autosomal genetic disease                       |
 |__autosomal dominant disease__________________|
                                                developmental and epileptic encephalopathy 103  2 rec.
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Is a autosomal dominant disease
developmental and epileptic encephalopathy
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Synonyms
  • "DEE103" EXACT OMO:0003012
    "early infantile epileptic encephalopathy 103" EXACT
Secondary IDs
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MIM:619913