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 99 ID (Ontology) DOID:0070385 (Human Disease)
Definition A developmental and epileptic encephalopathy characterized by onset of seizures in early childhood that has_material_basis_in heterozygous mutation in the ATP1A3 gene on chromosome 19q13.
Also Known As "DEE99" ; "early infantile epileptic encephalopathy 99"
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 Genes
 developmental and epileptic encephalopathy 99       2
 for disease ribbon | developmental and epileptic encephalopathy 99       2
 model of | developmental and epileptic encephalopathy 99       2
Spanning Tree (Parents/Children)
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electroclinical syndrome
 |__developmental and epileptic encephalopathy__
autosomal genetic disease                       |
 |__autosomal dominant disease__________________|
                                                developmental and epileptic encephalopathy 99  2 rec.
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Is a autosomal dominant disease
developmental and epileptic encephalopathy
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Synonyms
  • "DEE99" EXACT OMO:0003012
    "early infantile epileptic encephalopathy 99" EXACT
Secondary IDs
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MIM:619606