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DO Term : developmental and epileptic encephalopathy 15 [DOID:0080414] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A developmental and epileptic encephalopathy that has_material_basis_in homozygous or compound heterozygous mutation in the ST3GAL3 gene on chromosome 1p34.
  • synonyms:
  • early infantile epileptic encephalopathy 15,
  • DEE15,
  • OMIM:615006,
  • 615006
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents