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DO Term : familial temporal lobe epilepsy 8 [DOID:0060754] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A temporal lobe epilepsy characterized by autosomal dominant inheritance of complex partial seizures with occasional secondary generalization and that has_material_basis_in heterozygous mutation in the GAL gene on chromosome 11q13.
  • synonyms:
  • ORDO:101046,
  • 616461,
  • OMIM:616461,
  • ETL8
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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