Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:605751 - SEIZURES, BENIGN FAMILIAL INFANTILE, 2; BFIS2

Xenbase Genes: prrt2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011593 - maxillary tooth
MONDO:0017615 - vomerine dentition

Disease Ontology (DO):
DOID:0081115 - benign familial infantile seizures 2