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Human Disease

developmental and epileptic encephalopathy 75

Term ID
DOID:0112211
Synonyms
  • DEE75
  • early infantile epileptic encephalopathy 75
Definition
A developmental and epileptic encephalopathy characterized by onset in the first months of life of severe refractory seizures, multifocal spikes and hypsarrhythmia on EEG, severely impaired intellectual development with inability to walk, absent speech, and hypotonia with axial hyperreflexia that has_material_basis_in homozygous or compound heterozygous mutation in the PARS2 gene on chromosome 1p32.3. https://pubmed.ncbi.nlm.nih.gov/29915213/
References
Ontology
Human Disease   ( DOID:0112211 )
Relationships
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Genes Involved
Zebrafish Models