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Human Disease

developmental and epileptic encephalopathy 71

Term ID
DOID:0112207
Synonyms
  • DEE71
  • early infantile epileptic encephalopathy 71
  • glutaminase deficiency with neonatal epileptic encephalopathy
Definition
A developmental and epileptic encephalopathy characterized by early neonatal refractory seizures, respiratory failure, structural brain abnormalities and cerebral edema, with death within weeks after birth that has_material_basis_in homozygous or compound heterozygous mutation in GLS on chromosome 2q32.2. https://pubmed.ncbi.nlm.nih.gov/30575854/
References
Ontology
Human Disease   ( DOID:0112207 )
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