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DOID:0060751 - familial temporal lobe epilepsy 7
Disease Ontology Definition:A temporal lobe epilepsy characterized by autosomal dominant inheritance of focal seizures with prominent auditory symptoms and that has_material_basis_in heterozygous mutation in the RELN gene on chromosome 7q22.
Synonyms: ETL7,
Xenbase Genes : reln
MONDO:0014639 - frontal sulcus |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee