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Human Disease

developmental and epileptic encephalopathy 25

Term ID
DOID:0080453
Synonyms
  • DEE25
  • developmental and epileptic encephalopathy 25, with amelogenesis imperfecta
  • early infantile epileptic encephalopathy 25
Definition
A developmental and epileptic encephalopathy characterized by onset in early infancy of refractory seizures, global developmental delay with intellectual disability, persistent neurologic symptoms, and dental anomalies that has_material_basis_in homozygous or compound heterozygous mutation in the SLC13A5 gene on chromosome 17p13. (2)
References
Ontology
Human Disease   ( DOID:0080453 )
Relationships
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Genes Involved
Zebrafish Models