familial temporal lobe epilepsy 6

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Summary

Literature (0)

DOID:0060749 - familial temporal lobe epilepsy 6

Disease Ontology Definition:A temporal lobe epilepsy that has_material_basis_in variation in the chromosome region 3q25-q26.

Synonyms: ETL6,

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

:

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014308 - familial temporal lobe epilepsy 6

MONDO:0014308 - familial temporal lobe epilepsy 6

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant disease (is_a), temporal lobe epilepsy (is_a)