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Human Disease

developmental and epileptic encephalopathy 57

Term ID
DOID:0080284
Synonyms
  • DEE57
  • early infantile epileptic encephalopathy 57
Definition
A developmental and epileptic encephalopathy characterized by onset in the first days or months of life of refractory multifocal seizures, global developmental delay with hypotonia, variably impaired intellectual development, and poor or absent language that has_material_basis_in heterozygous mutation in the KCNT2 gene on chromosome 1q31. (3)
References
Ontology
Human Disease   ( DOID:0080284 )
Relationships
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Genes Involved
Zebrafish Models