benign familial infantile seizures 2

Summary

DOID:0081115 - benign familial infantile seizures 2

Disease Ontology Definition:A benign familial infantile epilepsy that is characterized by afebrile partial complex or generalized tonic-clonic seizures occurring between 3 and 12 months of age with a good response to medication and no neurologic sequelae and that has_material_basis_in mutation in the PRRT2 gene on chromosome 16p11.

Synonyms: Benign Familial Infantile Seizures, 2

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

: prrt2

MIM:

MIM:605751 - SEIZURES, BENIGN FAMILIAL INFANTILE, 2; BFIS2

MIM:605751 - SEIZURES, BENIGN FAMILIAL INFANTILE, 2; BFIS2

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), benign familial infantile epilepsy (is_a)