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Human Disease

developmental and epileptic encephalopathy 5

Term ID
DOID:0080438
Synonyms
  • DEE5
  • early infantile epileptic encephalopathy 5
Definition
A developmental and epileptic encephalopathy characterized by global developmental delay and onset in the first months of life of tonic seizures or infantile spasms that has_material_basis_in heterozygous mutation in the SPTAN1 gene on chromosome 9q34. https://www.ncbi.nlm.nih.gov/pubmed/20493457
References
Ontology
Human Disease   ( DOID:0080438 )
Relationships
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Genes Involved
Zebrafish Models