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DO Term : familial temporal lobe epilepsy 5 [DOID:0060752] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A temporal lobe epilepsy that has_material_basis_in heterozygous mutation in the CPA6 gene on chromosome 8q13.

synonyms:
ETL5,
ORDO:163717,
614417,
OMIM:614417

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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