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:300388 - POLYMICROGYRIA, BILATERAL PERISYLVIAN, X-LINKED; BPPX

Xenbase Genes: srpx2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010314 - structure with developmental contribution from neural crest
MONDO:0017091 - bilateral polymicrogyria
MONDO:0020340 - bilateral perisylvian polymicrogyria