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DO Term : familial temporal lobe epilepsy 2 [DOID:0060755] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A temporal lobe epilepsy characterized by autosomal dominant inheritance of complex or partial seizures and childhood febrile seizures that has_material_basis_in variation in the chromosome region 12q22-q23.3.
  • synonyms:
  • ORDO:98819,
  • 608096,
  • ETL2,
  • OMIM:608096
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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





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