familial temporal lobe epilepsy 2 Disease Ontology Browser

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Disease Ontology Browser

familial temporal lobe epilepsy 2 (DOID:0060755)
Alliance: disease page
Synonyms: ETL2
Alt IDs: OMIM:608096, ORDO:98819
Definition: 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.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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